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Graviola Max
(Annona Muricata & Annona Montana)

The normal price for Graviola Max (600 mg) $29.95
Special Pricing
(1 Bottle) 120 Capsules - $20.95ea - Save $8.00
(2 - 3 Bottles) 120 Capsules - $19.95 ea - Save $10.00
(4+ Bottles) 120 Capsules - $18.49 ea - Save $11.50
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Graviola Max
Graviola Max increases coverage of standard Graviola 100 % pure plant blend
of Graviola leaf and stem Annona Muricata, and Mountain Graviola leaf and stem
Annona Montana.
- Annona Muricata has 82 different acetogenins chemicals
- Annona Montana has 108 acetogenins chemicals. (Mountain type)
In a study, published in the Journal of Natural Products, scientists proved
that Graviola dramatically outperforms one of the most common chemotherapy drugs
on the market. You'll have all the scientific evidence that showed one chemical
in Graviola selectively kills colon cancer cells at "10,000 times the potency of
Adriamycin."
Other promising and ongoing research at Purdue University is supported by a
grant from the National Cancer Institute. Purdue researchers recently found that
leaves from the Graviola tree kills cancer cells "among six human-cell lines"
and are especially effective against prostate and pancreatic cancer cells.
In a separate study, Purdue researchers showed that extracts from the Graviola
leaves are extremely effective in isolating and killing lung cancer cells.
Some of the active ingredients
documented, researched, and verified in graviola are a group of Annonaceous
acetogenins which are only found in the Annonaceae plant family. Graviola (Annona
muricata) has 82 different acetogenin chemicals (in 10 distinct types).
Mountain graviola (Annona montana) contains the main annonacin chemical
that graviola does, and, it has 26 more acetogenin chemicals not found in
graviola (in 6 distinct types)! Graviola Max combines both species of graviola (Annona
muricata and Annona montana) to provide 12 different types of
acetogenins—108 distinct powerful chemicals in all. Compare that to only 28
acetogenin chemicals found in the American paw paw... Graviola Max delivers
almost four times more acetogenins than paw paw!
Family: Annonaceae
Genus: Annona
Species: Muricata
Synonyms: Annona macrocarpa, A. bonplandiana, A. cearensis,
Guanabanus muricatus
Common names: Graviola, soursop, Brazilian paw paw, guanábana,
guanábano, guanavana, guanaba, corossol épineux, huanaba, toge-banreisi, durian
benggala, nangka blanda, cachiman épineux
Part Used: Leaves, fruit, seeds, bark, roots
Suggested Use: Take 3 capsules 3 or 4 times daily or as directed by
a healthcare professional.
Contraindications:
 | Not to be used during pregnancy or breast-feeding. |
 | Graviola has demonstrated hypotensive, vasodilator, and
cardio-depressant activities in animal studies. People with low blood pressure
should monitor their blood pressure accordingly. |
Drug Interactions: None have been reported; however, based on animal
studies, Graviola may potentiate antihypertensive and cardiac depressant drugs.
Other Observations:
 | Graviola has demonstrated in vitro antimicrobial
properties. Chronic, long-term use of this plant might lead to some die-off of
friendly bacteria in the digestive tract. Supplementing the diet with
Probiotics and Digestive Enzymes may be helpful to counteract this possible
effect. |
 | Graviola has demonstrated emetic properties in one
animal study with pigs. Large single dosages may cause nausea or vomiting.
Reduce the usage accordingly or take with a meal if nausea occurs. |
 | Drinking plenty of water (at least 8 glasses a day) is
helpful to reduce Herxheimer reactions and flush dead and dying cells from the
body. |
 | One of three documented mechanisms of action of graviola is by decreasing
energy to abnormal cells (called an ATP-inhibitor). Taking supplements that
increase cellular energy (like CoQ10) will counteract or disable this one
mechanism of action of graviola (however, the other two mechanisms of action
will be unaffected). |
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GRAVIOLA
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HERBAL PROPERTIES
AND ACTIONS
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Main Actions |
Other Actions |
Standard Dosage |
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kills cancer cells |
relieves depression |
Leaves |
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slows tumor growth |
reduces spasms |
Infusion: 1 cup 3 times daily |
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kills bacteria |
kills viruses |
Tincture: 2-4 ml 3 times daily |
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kills parasites |
reduces fever |
Capsules: 2 g 3 times daily |
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reduces blood
pressure |
expels worms |
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lowers heart rate |
stimulates digestion |
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dilates blood vessels |
stops convulsions |
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sedates |
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Graviola is a small, upright evergreen tree, 5–6 m high, with
large, glossy, dark green leaves. It produces a large, heart-shaped, edible
fruit that is 15–20 cm in diameter, is yellow-green in color, and has white
flesh inside. Graviola is indigenous to most of the warmest tropical areas in
South and North America, including the Amazon. The fruit is sold in local
markets in the tropics, where it is called guanábana in Spanish-speaking
countries and graviola in Brazil. The fruit pulp is excellent for making
drinks and sherbets and, though slightly sour-acid, can be eaten out of hand.
Tribal & Herbal Medicine Uses
All parts of the graviola tree are used in natural medicine
in the tropics, including the bark, leaves, roots, fruit, and fruit seeds.
Different properties and uses are attributed to the different parts of the tree.
Generally, the fruit and fruit juice are taken for worms and parasites, to cool
fevers, to increase mother's milk after childbirth, and as an astringent for
diarrhea and dysentery. The crushed seeds are used against internal and external
parasites, head lice, and worms. The bark, leaves, and roots are considered
sedative, antispasmodic, hypotensive, and nervine, and a tea is made for various
disorders toward those effects.
Graviola has a long, rich history of use in herbal medicine
as well as a lengthy recorded indigenous use. In the Peruvian Andes, a leaf tea
is used for catarrh (inflammation of mucous membranes) and the crushed seed is
used to kill parasites. In the Peruvian Amazon the bark, roots, and leaves are
used for diabetes and as a sedative and antispasmodic. Indigenous tribes in
Guyana use a leaf and/or bark tea as a sedative and heart tonic. In the
Brazilian Amazon a leaf tea is used for liver problems, and the oil of the
leaves and unripe fruit is mixed with olive oil and used externally for
neuralgia, rheumatism, and arthritis pain. In Jamaica, Haiti, and the West
Indies the fruit and/or fruit juice is used for fevers, parasites and diarrhea;
the bark or leaf is used as an antispasmodic, sedative, and nervine for heart
conditions, coughs, flu, difficult childbirth, asthma, hypertension, and
parasites.
Plant Chemicals
Many
active compounds and chemicals have been found in graviola, as scientists have
been studying its properties since the 1940s. Most of the research on graviola
focuses on a novel set of chemicals called Annonaceous acetogenins.
Graviola produces these natural compounds in its leaf and stem, bark, and fruit
seeds. Three separate research groups have confirmed that these chemicals have
significant antitumorous properties and selective toxicity against various types
of cancer cells (without harming healthy cells) publishing eight clinical
studies on their findings. Many of the acetogenins have demonstrated selective
toxicity to tumor cells at very low dosages—as little as 1 part per million.
Four studies were published in 1998 which further specify the chemicals and
acetogenins in graviola which are demonstrating the strongest anticancerous,
antitumorous, and antiviral properties. In a 1997 clinical study, novel
alkaloids found in graviola fruit exhibited antidepressive effects in animals.
Annonaceous acetogenins are only found in the Annonaceae
family (to which graviola belongs). These chemicals in general have been
documented with antitumorous, antiparasitic, insecticidal, and antimicrobial
activities. Mode of action studies in three separate laboratories have recently
determined that these acetogenins are superb inhibitors of enzyme processes that
are only found in the membranes of cancerous tumor cells. This is why they are
toxic to cancer cells but have no toxicity to healthy cells. Purdue University,
in West Lafayette, Indiana, has conducted a great deal of the research on the
acetogenins, much of which, has been funded by The National Cancer Institute
and/or the National Institute of Health (NIH). Thus far, Purdue University
and/or its staff have filed at least nine U.S. and/or international patents on
their work around the antitumorous and insecticidal properties and uses of these
acetogenins.
In 1997, Purdue University published information with
promising news that several of the Annonaceous acetogenins were " . . . not only
are effective in killing tumors that have proven resistant to anti-cancer
agents, but also seem to have a special affinity for such resistant cells." In
several interviews after this information was publicized, the head
pharmacologist in Purdue's research explained how this worked. As he explains
it, cancer cells that survive chemotherapy can develop resistance to the agent
originally used as well as to other, even unrelated, drugs. This phenomenon is
called multi-drug resistance (MDR). One of the main ways that
cancer cells develop resistance to chemotherapy drugs is by creating an
intercellular pump which is capable of pushing anticancer agents out of the cell
before they can kill it. On average, only about two percent of the cancer cells
in any given person might develop this pump—but they are the two percent that
can eventually grow and expand to create multi-drug-resistant tumors. Some of
the latest research on acetogenins reported that they were capable of shutting
down these intercellular pumps, thereby killing multi-drug-resistant tumors.
Purdue researchers reported that the acetogenins preferentially killed
multi-drug-resistant cancer cells by blocking the transfer of ATP—the chief
source of cellular energy—into them. A tumor cell needs energy to grow and
reproduce, and a great deal more to run its pump and expel attacking agents. By
inhibiting energy to the cell , it can no longer run its pump. When acetogenins
block ATP to the tumor cell over time, the cell no longer has enough energy to
operate sustaining processes—and it dies. Normal cells seldom develop such a
pump; therefore, they don't require large amounts of energy to run a pump and,
generally, are not adversely affected by ATP inhibitors. Purdue researchers
reported that 14 different acetogenins tested thus far demonstrate potent
ATP-blocking properties (including several found only in graviola). They also
reported that 13 of these 14 acetogenins tested were more potent against MDR
breast cancer cells than all three of the standard drugs (adriamycin,
vincristine, and vinblastine) they used as controls.
The Annonaceous acetogenins discovered in graviola thus far
include: annocatalin, annohexocin, annomonicin, annomontacin, annomuricatin A &
B, annomuricin A thru E, annomutacin, annonacin, annonacinone, annopentocin A
thru C, cis-annonacin, cis-corossolone, cohibin A thru D, corepoxylone, coronin,
corossolin, corossolone, donhexocin, epomuricenin A & B, gigantetrocin,
gigantetrocin A & B, gigantetrocinone, gigantetronenin, goniothalamicin,
iso-annonacin, javoricin, montanacin, montecristin, muracin A thru G,
muricapentocin, muricatalicin, muricatalin, muri-catenol, muricatetrocin A & B
muricatin D, muricatocin A thru C muricin H, muricin I, muricoreacin,
murihexocin 3, murihexocin A thru C, murihexol, murisolin, robustocin,
rolliniastatin 1 & 2, saba-delin, solamin, uvariamicin I & IV, xylomaticin
Biological Activites and Clinical Research
In an 1976 plant screening program by the National Cancer
Institute, graviola leaves and stem showed active toxicity against cancer cells
and researchers have been following up on these findings since. Thus far,
specific acetogenins in graviola and/or extracts of graviola have been reported
to be selectively toxic in vitro to these types of tumor cells: lung
carcinoma cell lines; human breast solid tumor lines; prostate adenocarcinoma;
pancreatic carcinoma cell lines; colon adenocarcinoma cell lines; liver cancer
cell lines; human lymphoma cell lines; and multi-drug resistant human breast
adenocarcinoma. Researchers in Taiwan reported in 2003 that the main graviola
acetogenin, annonacin, was highly toxic to ovarian, cervical, breast,
bladder and skin cancer cell lines at very low dosages saying; “. . . annonacin
is a promising anti-cancer agent and worthy of further animal studies and, we
would hope, clinical trials.”
An interesting in vivo study was published in March of 2002 by
researchers in Japan, who were studying various acetogenins found in several
species of plants. They inoculated mice with lung cancer cells. One third
received nothing (the control group), one third received the chemotherapy drug
adriamycin, and one third received the main graviola acetogenin, annonacin (at
a dosage of 10 mg/kg). At the end of two weeks, five of the six in the
untreated control group were still alive and lung tumor sizes were then
measured. The adriamycin group showed a 54.6% reduction of tumor mass over the
control group—but 50% of the animals had died from toxicity (three of six).
The mice receiving annonacin were all still alive, and the tumors were
inhibited by 57.9%—slightly better than adriamycin—and without toxicity. This
led the researchers to summarize; “This suggested that annonacin was less
toxic in mice. On considering the antitumor activity and toxicity, annonacin
might be used as a lead to develop a potential anticancer agent.”
Current Practical Uses
Cancer research is ongoing on these important Annona
plants and plant chemicals, as several pharmaceutical companies and universities
continue to research, test, patent, and attempt to synthesize these chemicals
into new chemotherapeutic drugs. In fact, graviola seems to be following the
same path as another well known cancer drug – Taxol. From the time researchers
first discovered an antitumorous effect in the bark of the pacific yew tree and
a novel chemical called taxol was discovered in its bark - it took thirty years
of research by numerous pharmaceutical companies, universities, and government
agencies before the first FDA-approved Taxol drug was sold to a cancer patient
(which was based on the natural taxol chemical they found in the tree bark).
With graviola, it has taken researchers almost 10 years to successfully
synthesize (chemically reproduce) the main antitumorous chemical, annonacin.
These acetogenin chemicals have a unique waxy center and other unique molecular
energy properties which thwarted earlier attempts, and at least one major
pharmaceutical company gave up in the process (despite knowing how active the
natural chemical was against tumors). Now that scientists have the ability to
recreate this chemical and several other active acetogenins in the laboratory,
the next step is to change the chemical just enough (without losing any of the
antitumorous actions in the process) to become a novel chemical which can be
patented and turned into a new patented cancer drug. (Naturally-occurring plant
chemicals cannot be patented.) Thus far, scientists seem to be thwarted
again—every time they change the chemical enough to be patentable, they lose
much of the antitumorous actions. Like the development of taxol, it may well
take government agenies like the National Cancer Institute and the National
Institute of Health to step forward and launch full-scale human cancer research
on the synthesized unpatentable natural plant chemical (which will allow any
pharmaceutical company to develop a cancer drug utilizing the research as
happened with taxol) to be able to make this promising therapy available to
cancer patients in a timely fashion.
In the meantime, many cancer patients and health practitioners
are not waiting… they are adding the natural leaf and stem of
graviola (with over 40 documented naturally-occurring acetogenins including
annonacin) as a complementary therapy to their cancer protocols. After all,
graviola has a long history of safe use as a herbal remedy for other conditions
for many years, and research indicates that the antitumorous acetogenins are
selectively toxic to just cancer cells and not healthy cells—and in miniscule
amounts. While research confirms that these antitumorous acetogenins also occur
in high amounts in the fruit seeds and roots of graviola, different alkaloid
chemicals in the seeds and roots have shown some preliminary in vitro
neurotoxic effects. Researchers have suggested that these alkaloids might be
linked to atypical Parkinson’s disease in countries where the seeds are employed
as a common herbal parasite remedy. Therefore, using the seeds and root of
graviola is not recommended at this time.
The therapuetic dosage of graviola leaf, (which offers just
as high of an amount of acetogenins as the root and almost as much as the seed)
is reported to be 2-3 grams taken 3 or 4 times daily. Graviola products
(capsules and tinctures) are becoming more widely available in the U.S. market,
and now offered under several different manufacturer’s labels in health food
stores. As one of graviola’s mechanisms of action is to deplete ATP energy to
cancer cells, combining it with other supplements and natural products which
increase or enhance cellular ATP may reduce the effect of graviola. The main
supplement which increases ATP is a common antioxidant called Coenzyme Q10 and
for this reason, it should be avoided when taking graviola.
Graviola is certainly a promising natural remedy and one that
again emphasizes the importance of preserving our remaining rainforest
ecosystems. Perhaps—if enough people believe that the possible cure for cancer
truly is locked away in a rainforest plant—we will take the steps needed to
protect our remaining rainforests from destruction. One researcher studying
graviola summarized this idea eloquently: “At the time of preparation of this
current review, over 350 Annonaceous acetogenins have been isolated from 37
species. Our preliminary efforts show that about 50%, of over 80 Annonaceous
species screened, are significantly bioactive and are worthy of fractionation;
thus, this class of compounds can be expected to continue to grow at an
exponential rate in the future, provided that financial support for such
research efforts can be found. With the demise of the world’s tropical rain
forests, such work is compelling before the great chemical diversity, contained
within these endangered species, is lost.”
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GRAVIOLA PLANT SUMMARY
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Main
Actions (in order):
anticancerous, antitumorous, antimicrobial, antiparasitic, hypotensive
(lowers blood pressure)
Main Uses:
- for cancer (all types)
- as a broad-spectrum internal and external antimicrobial to treat
bacterial and fungal infections
- for internal parasites and worms
- for high blood pressure
- for depression, stress, and nervous disorders
Properties/Actions Documented by Research:
antibacterial, anticancerous, anticonvulsant, antidepressant, antifungal,
antimalarial, antimutagenic (cellular protector), antiparasitic,
antispasmodic, antitumorous, cardiodepressant, emetic (causes vomiting),
hypotensive (lowers blood pressure), insecticidal, sedative, uterine
stimulant, vasodilator
Other Properties/Actions Documented by Traditional Use:
antiviral, cardiotonic (tones, balances, strengthens the heart),
decongestant, digestive stimulant, febrifuge (reduces fever), nervine
(balances/calms nerves), pediculicide (kills lice), vermifuge (expels worms)
Cautions: It has cardiodepressant, vasodilator, and hypotensive
(lowers blood pressure) actions. Large dosages can cause nausea and
vomiting. Avoid combining with ATP-enhancers like CoQ10. |
Traditional Preparation: The therapeutic
dosage is reported to be 2 g three times daily in capsules or tablets. A
standard infusion (one cup 3 times daily) or a 4:1 standard tincture (2–4 ml
three times daily) can be substituted if desired. See Traditional Herbal
Remedies Preparation Methods page if necessary for definitions.
Contraindications:
 | Graviola has demonstrated uterine stimulant activity in an animal study
(rats) and should therefore not be used during pregnancy.
|
 | Graviola has demonstrated hypotensive, vasodilator, and cardiodepressant
activities in animal studies and is contraindicated for people with low blood
pressure. People taking antihypertensive drugs should check with their doctors
before taking Graviola and monitor their blood pressure accordingly (as
medications may need adjusting).
|
 | Graviola has demonstrated significant in vitro antimicrobial
properties. Chronic, long-term use of this plant may lead to die-off of
friendly bacteria in the digestive tract due to its antimicrobial properties.
Supplementing the diet with Probiotics and Digestive Enzymes is advisable if
this plant is used for longer than 30 days.
|
 | Graviola has demonstrated emetic properties in one animal study with pigs.
Large single dosages may cause nausea or vomiting. Reduce the usage
accordingly if this occurs.
|
 | One study with rats given a stem-bark extract intragastrically (at 100
mg/kg) reported an increase in dopamine, norepinephrine, and monomine oxidase
activity, as well as a inhibition of serotonin release in stress-induced rats.
|
 | Alcohol extracts of Graviola leaf showed no toxicity or side effects in
mice at 100 mg/kg; however, at a dosage of 300 mg/kg, a reduction in
explorative behavior and mild abdominal constrictions was observed. If
sedation or sleepiness occurs, reduce the amount used. |
Drug Interactions: None have been reported;
however, Graviola may potentiate antihypertensive and cardiac depressant drugs.
It may potentiate antidepressant drugs and interfere with MAO-inhibitor drugs.
See contraindications above.
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WORLDWIDE
ETHNOMEDICAL USES
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| Brazil |
for abscesses,
bronchitis, chest problems, cough, diabetes, diarrhea, dysentery, edema,
fever, intestinal colic, intestinal parasites, liver problems, neuralgia,
nervousness, pain, parasites, rheumatism, spasms, worms |
| Caribbean |
for chills, fever,
flu, indigestion, nervousness, palpitations, rash, spasms, skin disease, and
as a sedative |
| Curaçao |
for childbirth,
gallbladder problems, nervousness, and as a sedative and tranquilizer |
| Haiti |
for digestive
sluggishness, coughs, diarrhea, fever, flu, heart conditions, lactation aid,
lice, nerves, parasites, pain, pellagra, sores, spasms, weakness, wounds,
and as a sedative |
| Jamaica |
for asthma, fevers,
heart conditions, hypertension, lactation aid, nervousness, parasites,
spasms, water retention, weakness, worms, and as a sedative |
| Malaysia |
for boils, coughs,
diarrhea, dermatosis, hypertension, rheumatism, and to reduce bleeding |
| Mexico |
for diarrhea,
dysentery, fever, chest colds, ringworm, scurvy, and to reduce bleeding |
| Panama |
for diarrhea,
dyspepsia, kidney, stomach ulcers, worms |
| Peru |
for diabetes,
diarrhea, dysentery, fever, hypertension, indigestion, inflammation, lice,
liver disorders, parasites, spasms, tumors, ulcers (internal), and as a
sedative |
| Trinidad |
for blood cleansing,
fainting, flu, high blood pressure, insomnia, lactation aid, palpitations,
ringworms |
| U.S.A. |
for cancer,
depression, fungal infections, hypertension, intestinal parasites, tumors |
| West Indies |
for asthma,
childbirth, diarrhea, hypertension, lactation aid, parasites, worms |
| Elsewhere |
for arthritis,
asthma, bile insufficiency, childbirth, cancer, diarrhea, dysentery, fever,
heart problems, kidney problems, lactation aid, lice, liver disorders,
malaria, pain, ringworm, scurvy, stomach problems, and as a sedative |
Third-Party Published Research on Graviola
All available third-party documentation
and research on Graviola be found at
PubMed. A partial listing of the third-party published research on
Graviola is shown below:
Anticancerous & Antitumor Actions:
Kojima, N. “Systematic synthesis of antitumor Annonaceous acetogenins”
Yakugaku Zasshi. 2004; 124(10): 673-81.
Tormo, J. R., et al. “In vitro antitumor structure-activity relationships
of threo/trans/threo mono-tetrahydro-furanic acetogenins: Correlations with
their inhibition of mitochondrial complex I.” Oncol. Res. 2003; 14(3):
147-54.
Yuan, S. S., et al. “Annonacin, a mono-tetrahydrofuran acetogenin, arrests
cancer cells at the G1 phase and causes cytotoxicity in a Bax- and
caspase-3-related pathway.” Life Sci. 2003 May: 72(25): 2853-61.
Liaw, C. C., et al. “New cytotoxic monotetrahydrofuran Annonaceous acetogenins
from Annona muricata.” J. Nat. Prod. 2002; 65(4): 470-75
Gonzalez-Coloma, A., et al. “Selective action of acetogenin mitochondrial
complex I inhibitors.” Z. Naturforsch. 2002; 57(11-12): 1028-34.
Chang, F. R., et al. “Novel cytotoxic Annonaceous acetogenins from Annona
muricata.” J. Nat. Prod. 2001; 64(7): 925-31.
Jaramillo, M. C., et al. “Cytotoxicity and antileishmanial activity of Annona
muricata pericarp.” Fitoterapia. 2000; 71 (2): 183-6.
Betancur-Galvis, L., et al. “Antitumor and antiviral activity of Colombian
medicinal plant extracts.” Mem. Inst. Oswaldo Cruz. 1999; 94(4): 531-35.
Kim, G. S., et al. “Muricoreacin and murihexocin C, mono-tetrahydrofuran
acetogenins, from the leaves of Annona muricata.” Phytochemistry.
1998; 49(2): 565-71.
Kim, G. S., et al. “Two new mono-tetrahydrofuran ring acetogenins, annomuricin E
and muricapentocin, from the leaves of Annona muricata.” J. Nat. Prod.
1998; 61(4): 432-36.
Nicolas, H., et al. “Structure-activity relationships of diverse Annonaceous
acetogenins against multidrug resistant human mammary adenocarcinoma (MCF-7/Adr)
cells.” J. Med. Chem. 1997; 40(13): 2102-6.
Zeng, L., et al. “Five new monotetrahydrofuran ring acetogenins from the leaves
of Annona muricata.” J. Nat. Prod. 1996; 59(11): 1035-42.
Wu, F. E., et al. “Two new cytotoxic monotetrahydrofuran Annonaceous acetogenins,
annomuricins A and B, from the leaves of Annona muricata.” J. Nat.
Prod. 1995; 58(6): 830-36.
Oberlies, N. H., et al. “Tumor cell growth inhibition by several Annonaceous
acetogenins in an in vitro disk diffusion assay.” Cancer Lett.
1995; 96(1): 55-62.
Wu, F. E., et al. “Additional bioactive acetogenins, annomutacin and (2,4-trans
and cis)-10R-annonacin-A-ones, from the leaves of Annona muricata.” J.
Nat. Prod. 1995; 58(9): 1430-37.
Wu, F. E., et al. “New bioactive monotetrahydrofuran Annonaceous acetogenins,
annomuricin C and muricatocin C, from the leaves of Annona muricata.”
J. Nat. Prod. 1995; 58(6): 909-5.
Wu, F. E., et al. “Muricatocins A and B, two new bioactive monotetrahydrofuran
Annonaceous acetogenins from the leaves of Annona muricata.” J. Nat.
Prod. 1995; 58(6): 902-8.
Sundarrao, K., et al. “Preliminary screening of antibacterial and antitumor
activities of Papua New Guinean native medicinal plants.” Int. J. Pharmacog.
1993; 31(1): 3-6.
Antimicrobial Actions:
Takahashi, J.A., et al. “Antibacterial activity of eight Brazilian Annonaceae
plants.” Nat. Prod. Res. 2006; 20(1): 21-6.
Betancur-Galvis, L., et al. “Antitumor and antiviral activity of Colombian
medicinal plant extracts.” Mem. Inst. Oswaldo Cruz 1999; 94(4): 531-35.
Antoun, M. D., et al. "Evaluation of the flora of Puerto Rico for in vitro
cytotoxic and anti-HIV activities." Pharmaceutical Biol. 1999; 37(4):
277-280.
Padma, P., et al. “Effect of the extract of Annona muricata and
Petunia nyctaginiflora on Herpes simplex virus.” J. Ethnopharmacol.
1998; 61(1): 81–3.
Sundarrao, K., et al. “Preliminary screening of antibacterial and antitumor
activities of Papua New Guinean native medicinal plants.” Int. J. Pharmacog.
1993; 31(1): 3–6.
Misas, C. A. J., et al. “Contribution to the biological evaluation of Cuban
plants. IV.” Rev. Cubana Med. Trop. 1979; 31(1): 29–35.
Antidepressant & Antistress Actions:
Padma, P., et al. “Effect of Annona muricata and Polyalthia cerasoides
on brain neurotransmitters and enzyme monoamine oxidase following cold
immobilization stress.” J. Natural Remedies 2001; 1(2): 144–46.
Hasrat, J. A., et al. “Screening of medicinal plants from Suriname for 5-HT 1A
ligands: Bioactive isoquinoline alkaloids from the fruit of Annona muricata.”
Phytomedicine. 1997; 4(20: 133-140.
Padma, P., et al. “Effect of alcohol extract of Annona muricata on cold
immobilization stress induced tissue lipid peroxidation.” Phytother. Res.
1997; 11(4): 326-327.
Hasrat, J. A., et al. “Isoquinoline derivatives isolated from the fruit of
Annona muricata as 5-HTergic 5-HT1A receptor agonists in rats: unexploited
antidepressive (lead) products.” J. Pharm. Pharmacol. 1997; 49(11):
1145–49.
Antiparasitic, Antimalarial, & Insecticidal Actions:
Luna, J. S., et al. “Acetogenins in Annona muricata L. (Annonaceae)
leaves are potent molluscicides.” Nat. Prod. Res. 2006; 20(3): 253-7.
Jaramillo, M. C., et al. “Cytotoxicity and antileishmanial activity of Annona
muricata pericarp.” Fitoterapia. 2000; 71(2): 183–6.
Alali, F. Q., et al. “Annonaceous acetogenins as natural pesticides; potent
toxicity against insecticide-susceptible and resistant German cockroaches (Dictyoptera:
Blattellidae).” J. Econ. Entomol. 1998; 91(3): 641-9.
Antoun, M. D., et al. "Screening of the flora of Puerto Rico for potential
antimalarial bioactives.” Int. J. Pharmacog. 1993; 31(4): 255–58.
Heinrich, M., et al. “Parasitological and microbiological evaluation of Mixe
Indian medicinal plants (Mexico).” J. Ethnopharmacol. 1992; 36(1): 81–5.
Bories, C., et al. “Antiparasitic activity of Annona muricata and
Annona cherimolia seeds.” Planta Med. 1991; 57(5): 434–36.
Gbeassor, M., et al. “In vitro antimalarial activity of six medicinal
plants.” Phytother. Res. 1990; 4(3): 115–17.
Tattersfield, F., et al. “The insecticidal properties of certain species of
Annona and an Indian strain of Mundulea sericea (Supli).” Ann.
Appl. Biol. 1940; 27: 262–73.
Anticonvulsant, Antispasmodic, & Smooth Muscle Relaxant Actions:
N’gouemo, P., et al. “Effects of ethanol extract of Annona muricata on
pentylenetetrazol-induced convulsive seizures in mice.” Phytother. Res.
1997; 11(3): 243–45.
Feng, P. C., et al. “Pharmacological screening of some West Indian medicinal
plants.” J. Pharm. Pharmacol. 1962; 14: 556–61.
Hypotensive & Cardiodepressant Actions
Carbajal, D., et al. “Pharmacological screening of plant decoctions commonly
used in Cuban folk medicine.” J. Ethnopharmacol. 1991; 33(1/2): 21–4.
Feng, P. C., et al. “Pharmacological screening of some West Indian medicinal
plants.” J. Pharm. Pharmacol. 1962; 14: 556–61.
Meyer, T. M. “The alkaloids of Annona muricata.” Ing. Ned. Indie.
1941; 8(6): 64.

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