Liquid extracts cited in the numerous studies indicated selective
cytotoxicities against several cancer cell lines*. The phytochemicals
are derived from the leaf of this popular tropical fruit tree. Studies
below point to its reputation and popular use by herbalists. Historical
ethnobotanical use is said to be sedative and anti-spasmodic. Sometimes
used to treat, cleanse and support the liver, treat catarrh, and
considered anthelmintic, antidiuretic, anti-asthmatic and digestive.
(References below).
Suggested Use: Liquids:
Use 15-20 drops mixed with water two to three times daily, or more as
recommended by a practitioner. Capsules: Two capsules
once or twice daily; Tea: One tsp loose leaf per 16 oz
of boiling water.
Cautions: Use under care/advice of a
medical practitioner. Not intended for long term therapy.
Contraindications:Should not be used during
pregnancy. It is not recommended for people with low blood pressure,
can have a hypotensive, vasodilator and cardio depressant action. May
potentiate antihypertensive and cardiac depressant drugs. It may
potentiate antidepressant drugs. People using antihypertensive drugs
should monitor blood pressure and adjust medications if necessary. Do
not use in combination with MAO inhibitors and some types of
prescription antidepressants. Long-term use may disrupt bacteria in the
digestive tract. Can promote drowsiness. Reduce the amount used if
feeling tired.
Ingredients:
100% Graviola leaf extracted in distilled water and 40% organic grain
alcohol. Full spectrum powders are in vegi-caps.
More About Graviola:
1. Novel cytotoxic
annonaceous acetogenins from Annona muricata
J Nat Prod. 1995 Sep;58(9):1430-7. Department of Medicinal Chemistry and
Pharmacognosy, School of Pharmacy and Pharmacal Sciences, Purdue
University, West Lafayette, Indiana 47907, USA.
2. Isolation and characterization of a lectin from
Annona muricata seeds
Damico DC, Freire MG, Gomes VM, Toyama MH, Marangoni S, Novello JC,
Macedo ML.
Departamento de Bioquimica, Instituto de Biologia, Universidade Estadual
de Campinas, Campinas (SP), Brazil.
J Protein Chem. 2003 Nov;22(7-8):655-61.
3. Effect of the extract of Annona muricata and
Petunia nyctaginiflora on Herpes simplex virus.
Padma P, Pramod NP, Thyagarajan SP, Khosa RL.
Department of Pharmaceutics, IT, Banaras Hindu University, Varanasi,
India.
Annona muricata (Annonaceae) and Petunia nyctaginiflora (Solanaceae)
were screened for their activity against Herpes simplex virus-1 (HSV-1)
and clinical isolate (obtained from the human keratitis lesion). We have
looked at the ability of extract(s) to inhibit the cytopathic effect of
HSV-1 on vero cells as indicative of anti-HSV-1 potential. The minimum
inhibitory concentration of ethanolic extract of A. muricata and aqueous
extract of P. nyctaginiflora was found to be 1 mg/ml.
4. Novel cytotoxic annonaceous acetogenins from
Annona muricata.
Chang FR, Wu YC.
Graduate Institute of Natural Products, Kaohsiung Medical University,
Kaohsiung 807, Taiwan, Republic of China.
J Nat Prod. 2001 Jul;64(7):925-31.
PMID: 11473425 [PubMed - indexed for MEDLINE]
5. Isolation and characterization of a lectin from
Annona muricata seeds.
Damico DC, Freire MG, Gomes VM, Toyama MH, Marangoni S, Novello JC,
Macedo ML.
Departamento de Bioquimica, Instituto de Biologia, Universidade
Estadual de Campinas, Campinas (SP), Brazil.
J Protein Chem. 2003 Nov;22(7-8):655-61.
PMID: 14714732 [PubMed - in process]
6. [Studies on the chemical constituents of Annona
muricata] [Article in Chinese]
Yu JG, Gui HQ, Luo XZ, Sun L, Zhu P, Yu ZL.
Institute of Medicinal Plant Development, Chinese Academy of Medical
Sciences and Peking Union Medical College, Beijing 100094.
Yao Xue Xue Bao. 1997 Jun;32(6):431-7.
PMID: 11596323 [PubMed - indexed for MEDLINE]
7. New cytotoxic monotetrahydrofuran annonaceous
acetogenins from Annona muricata.
Liaw CC, Chang FR, Lin CY, Chou CJ, Chiu HF, Wu MJ, Wu YC.
Graduate Institute of Natural Products, Kaohsiung Medical University,
Kaohsiung 807, Taiwan, Republic of China.
J Nat Prod. 2002 Apr;65(4):470-5.
8. Additional bioactive acetogenins, annomutacin and
(2,4-trans and cis)-10R-annonacin-A-ones, from the leaves of Annona
muricata.
Wu FE, Zhao GX, Zeng L, Zhang Y, Schwedler JT, McLaughlin JL,
Sastrodihardjo S.
Department of Medicinal Chemistry and Pharmacognosy, School of
Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette,
Indiana 47907, USA.
J Nat Prod. 1995 Sep;58(9):1430-7.
1. Novel cytotoxic annonaceous acetogenins from
Annona muricata.
Chang FR, Wu YC.
Graduate Institute of Natural Products, Kaohsiung Medical University,
Kaohsiung 807, Taiwan, Republic of China.
J Nat Prod. 2001 Jul;64(7):925-31.
Seven new annonaceous acetogenins, muricins A-G (1-7), as well as five
known compounds, a mixture of muricatetrocin A (8) and muricatetrocin B
(9), longifolicin (10), corossolin (11), and corossolone (12), were
isolated from the seeds of Annona muricata. The structures of all
isolates were elucidated and characterized by spectral and chemical
methods. These acetogenins showed significantly selective in vitro
cytotoxicities toward the human hepatoma cell lines Hep G(2) and 2,2,15.
PMID: 11473425 [PubMed - indexed for MEDLINE]
2. Isolation and characterization of a lectin from
Annona muricata seeds.
Damico DC, Freire MG, Gomes VM, Toyama MH, Marangoni S, Novello JC,
Macedo ML.
Departamento de Bioquimica, Instituto de Biologia, Universidade
Estadual de Campinas, Campinas (SP), Brazil.
J Protein Chem. 2003 Nov;22(7-8):655-61.
A lectin with a high affinity for glucose/mannose was isolated from
Annona muricata seeds (Annonaceae) by gel filtration chromatography on
Sephacryl S-200, ion exchange chromatography on a DEAE SP-5 PW column,
and molecular exclusion on a Protein Pak Glass 300 SW column. Sodium
dodecyl sulfate polyacrylamide gel electrophoresis (PAGE) yielded two
protein bands of approximately 14 kDa and 22 kDa. However, only one band
was seen in native PAGE. The Mr of the lectin estimated by
fast-performance liquid chromatography-gel filtration on Superdex 75 was
22 kDa. The lectin was a glycoprotein with 8% carbohydrate (neutral
sugar) and required divalent metal cations (Ca2+, Mg2+, and Mn2+) for
full activity. Amino acid analysis revealed a large content of Glx, Gly,
Phe, and Lys. The lectin agglutinated dog, chicken, horse, goose, and
human erythrocytes and inhibited the growth of the fungi Fusarium
oxysporum, Fusarium solani, and Colletotrichum musae.
PMID: 14714732 [PubMed - in process]
3. [Studies on the chemical constituents of Annona
muricata] [Article in Chinese]
Yu JG, Gui HQ, Luo XZ, Sun L, Zhu P, Yu ZL.
Institute of Medicinal Plant Development, Chinese Academy of Medical
Sciences and Peking Union Medical College, Beijing 100094.
Yao Xue Xue Bao. 1997 Jun;32(6):431-7.
Annonaceous acetogenin (or polyketide) is a kind of potential
antineoplastic agents from Annonaceae plants. Two new acetogenins,
Muricatalicin (I) and muricatalin (VI), a mesitoate of a new acetogenin,
annonacin-B mesitoate (Vb), and three known acetogenins, annonacin
(II), annonacin-A (III) and annonacin-10-one (IV) have been isolated
from Annona muricata L. The structures and relative stereochemistry of
I, VI and Vb were elucidated on the basis of spectral analysis and
examination of their acetates and/or mesitoate.
PMID: 11596323 [PubMed - indexed for MEDLINE]
4. Effect of the extract of Annona muricata and
Petunia nyctaginiflora on Herpes simplex virus.
Padma P, Pramod NP, Thyagarajan SP, Khosa RL.
Department of Pharmaceutics, IT, Banaras Hindu University, Varanasi,
India.
J Ethnopharmacol. 1998 May;61(1):81-3.
Annona muricata (Annonaceae) and Petunia nyctaginiflora (Solanaceae)
were screened for their activity against Herpes simplex virus-1 (HSV-1)
and clinical isolate (obtained from the human keratitis lesion). We have
looked at the ability of extract(s) to inhibit the cytopathic effect of
HSV-1 on vero cells as indicative of anti-HSV-1 potential. The minimum
inhibitory concentration of ethanolic extract of A. muricata and aqueous
extract of P. nyctaginiflora was found to be 1 mg/ml.
PMID: 9687085 [PubMed - indexed for MEDLINE]
5. New cytotoxic monotetrahydrofuran annonaceous
acetogenins from Annona muricata.
Liaw CC, Chang FR, Lin CY, Chou CJ, Chiu HF, Wu MJ, Wu YC.
Graduate Institute of Natural Products, Kaohsiung Medical University,
Kaohsiung 807, Taiwan, Republic of China.
J Nat Prod. 2002 Apr;65(4):470-5.
Three new monotetrahydrofuran annonaceous acetogenins, muricin H (1),
muricin I (2), and cis-annomontacin (3), along with five known
acetogenins, annonacin, annonacinone, annomontacin, murisolin, and
xylomaticin, were isolated from the seeds of Annona muricata.
Additionally, two new monotetrahydrofuran annonaceous acetogenins,
cis-corossolone (4) and annocatalin (5), together with four known ones,
annonacin, annonacinone, solamin, and corossolone, were isolated from
the leaves of this species. The structures of all new isolates were
elucidated and characterized by spectral and chemical methods. These new
acetogenins exhibited significant activity in in vitro cytotoxic assays
against two human hepatoma cell lines, Hep G(2) and 2,2,15. Compound 5
showed a high selectivity toward the Hep 2,2,15 cell line.
6. Additional bioactive acetogenins, annomutacin and
(2,4-trans and cis)-10R-annonacin-A-ones, from the leaves of Annona
muricata.
Wu FE, Zhao GX, Zeng L, Zhang Y, Schwedler JT, McLaughlin JL,
Sastrodihardjo S.
Department of Medicinal Chemistry and Pharmacognosy, School of
Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette,
Indiana 47907, USA.
J Nat Prod. 1995 Sep;58(9):1430-7.
In a continuation of our research on bioactive components from the
leaves of Annona muricata, three novel monotetrahydrofuran Annonaceous
acetogenins, namely, annomutacin [1], (2,4-trans)-10R-annonacin-A-one
[2], and (2,4-cis)-10R- annonacin-A-one [3], have been identified. Their
structures were deduced by ms, nmr, ir, and uv spectral and chemical
methods, and the absolute configurations were determined by Mosher ester
methodology. A known bioactive amide, N-p-coumaroyl tyramine, was also
found. Compound 1 and the mixture of compounds 2 and 3 showed selective
cytotoxicities against the human A-549 lung tumor cell line.
Disclaimer: Statements on this page
have not been evaluated by the Food and Drug Administration. This
product is not intended to diagnose, treat, cure or prevent any disease.
Information on this publication should not be used as medical advice.
Data prvided for research and professional use only