Scientific name	Authority	First published in
Blaberopus venenatus	A.DC.	Prodr. 8: 411 (1844)
Echites venenatus	Roxb.	Hort. Bengal. 20; et ex A. DC. in DC. Prod. viii. 411.
Alstonia venenata var. pubescens	Monach.	Pacific Sci. 3: 156. 1949

Common names Top

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Language	Common/alternative name
Malayalam	അണലിവേഗം
Chinese	毒糖胶树
Chinese	毒糖膠樹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-tropical click to expand
- Indian Subcontinent
  - India

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000953155
Tropicos	1800002
KEW	urn:lsid:ipni.org:names:76602-1
The Plant List	kew-7123
Open Tree Of Life	463397
NCBI Taxonomy	994907
IPNI	76602-1
iNaturalist	430637
GBIF	5535596
Freebase	/m/0w33tqd
EPPO	ATNVE
USDA GRIN	2689
Wikipedia	Alstonia_venenata

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Investigation of Small-Molecule Constituents in Voacanga africana Seeds and Mapping of Their Spatial Distributions Using Laser Ablation Direct Analysis in Real-Time Imaging–Mass Spectrometry (LADI-MS)

Coon AM, Musah RA

ACS Omega

18-Jul-2023

PMCID:	PMC10399170
doi:	10.1021/acsomega.3c02464
PMID:	37546641

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Anticancer Potential of Natural Bark Products—A Review

Burlacu E, Tanase C

Plants (Basel)

13-Sep-2021

PMCID:	PMC8467168
doi:	10.3390/plants10091895
PMID:	34579427

Infrequent use of medicinal plants from India in snakebite treatment

Upasani MS, Upasani SV, Beldar VG, Beldar CG, Gujarathi PP

Integr Med Res

06-Nov-2017

PMCID:	PMC5884010
doi:	10.1016/j.imr.2017.10.003
PMID:	29629287

Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence

Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD

Evid Based Complement Alternat Med

21-Aug-2017

PMCID:	PMC5585606
doi:	10.1155/2017/5748256
PMID:	28904556

Ethnomedicinal plants used for snakebite in India: a brief overview

Upasani SV, Beldar VG, Tatiya AU, Upasani MS, Surana SJ, Patil DS

Integr Med Res

20-Mar-2017

PMCID:	PMC5478250
doi:	10.1016/j.imr.2017.03.001
PMID:	28664135

Ethnomedicinal assessment of Irula tribes of Walayar valley of Southern Western Ghats, India

Venkatachalapathi A, Sangeeth T, Ali MA, Tamilselvi SS, Paulsamy S, Al-Hemaidc FM

Saudi J Biol Sci

19-Oct-2016

PMCID:	PMC5936975
doi:	10.1016/j.sjbs.2016.10.011
PMID:	29740242

ChemInform Abstract: STRUCTURE AND ABSOLUTE STEREOCHEMISTRY OF 19‐EPI‐(+)‐ECHITOVENILINE. A NEW INDOLE ALKALOID OF THE LEAVES OF ALSTONIA VENENATA R.BR

P. L. MAJUMDER, S. JOARDAR, B. N. DINDA, D. BANDYOPADHYAY, S. JOARDAR, A. BASU

Wiley

24-Apr-2016

doi:	10.1002/CHIN.198128353

Large Scale Screening of Ethnomedicinal Plants for Identification of Potential Antibacterial Compounds

Panda SK, Mohanta YK, Padhi L, Park YH, Mohanta TK, Bae H

Molecules

14-Mar-2016

PMCID:	PMC6274442
doi:	10.3390/molecules21030293
PMID:	26985889

Pd(OAc)2-catalyzed dehydrogenative C–H activation: An expedient synthesis of uracil-annulated β-carbolinones

Mondal B, Hazra S, Panda TK, Roy B

Beilstein J Org Chem

04-Aug-2015

PMCID:	PMC4578345
doi:	10.3762/bjoc.11.146
PMID:	26425190

Quantification of Plant Chlorophyll Content Using Google Glass

Cortazar B, Koydemir HC, Tseng D, Feng S, Ozcan A

Lab Chip

11-Feb-2015

PMCID:	PMC4366296
doi:	10.1039/c4lc01279h
PMID:	25669673

Antifungal Indole and Pyrrolidine-2,4-Dione Derivative Peptidomimetic Lead Design Based on In Silico Study of Bioactive Peptide Families

Moradi S, Azerang P, Khalaj V, Sardari S

Avicenna J Med Biotechnol

01-Jan-2013

PMCID:	PMC3572706
PMID:	23626876

Rigorous Biogenetic Network for a Group of Indole Alkaloids Derived from Strictosidine

Szabó LF

Molecules

27-Aug-2008

PMCID:	PMC6245392
doi:	10.3390/molecules13081875
PMID:	18794791

Antifungal Activity of Nor-securinine Against Some Phytopathogenic Fungi

Sahni S, Maurya S, Singh UP, Singh AK, Singh VP, Pandey VB

Mycobiology

30-Jun-2005

PMCID:	PMC3774870
doi:	10.4489/MYCO.2005.33.2.097
PMID:	24049481

The alkaloids of the fruits of R.Br. echitovenidine and (+)-minovincinine

B. Das, K. Biemann, A. Chatterjee, A.B. Ray, P.L. Majumder

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4039(00)75680-2

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Ajmaline-sarpagine alkaloids
3Dff5qdk46	15599715	Click to see CC1C(C2CC3N1C4C2C(C5(C4)C3=NC6=CC=CC=C56)OC(=O)C)CO	352.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
> Alkaloids and derivatives / Aspidofractine alkaloids
Methyl (9R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate	21123851	Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4	338.40	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
19S-hydroxy-(+)-vincadifformine	138911112	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O	354.40	unknown	https://doi.org/10.1016/S0040-4039(00)75680-2
methyl (1R,12R,19R)-12-[(1R)-1-(3-methylbut-2-enoyloxy)ethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	134714947	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C=C(C)C	436.50	unknown	https://doi.org/10.1016/S0040-4039(00)75680-2
methyl (1R,12R,19R)-5-methoxy-12-[(1S)-1-(7-methoxy-1,3-benzodioxole-5-carbonyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9-tetraene-10-carboxylate	162913847	Click to see CC(C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC)OC(=O)C6=CC7=C(C(=C6)OC)OCO7	562.60	unknown	https://doi.org/10.1016/S0040-4020(01)97441-1
methyl (1S,12S,19S)-12-[(1R)-1-(3,4,5-trimethoxybenzoyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	162885869	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	548.60	unknown	https://doi.org/10.1002/CHIN.198128353
methyl (1S,12S,19S)-12-[(1S)-1-(7-methoxy-1,3-benzodioxole-5-carbonyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	162926770	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC7=C(C(=C6)OC)OCO7	532.60	unknown	https://doi.org/10.1016/S0031-9422(00)91368-2
Methyl 12-[1-(3,4,5-trimethoxybenzoyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	155886207	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	548.60	unknown	https://doi.org/10.1002/CHIN.198128353
Methyl 12-[1-(7-methoxy-1,3-benzodioxole-5-carbonyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	162926769	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC7=C(C(=C6)OC)OCO7	532.60	unknown	https://doi.org/10.1016/S0031-9422(00)91368-2
Methyl 5-methoxy-12-[1-(7-methoxy-1,3-benzodioxole-5-carbonyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9-tetraene-10-carboxylate	162913845	Click to see CC(C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC)OC(=O)C6=CC7=C(C(=C6)OC)OCO7	562.60	unknown	https://doi.org/10.1016/S0040-4020(01)97441-1
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (1S,10R,12S,13R,14S,15R)-15-ethyl-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate	163006424	Click to see CCC1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC	354.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
methyl (1S,10R,12S,13S,14S,15R)-15-ethyl-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate	163006425	Click to see CCC1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC	354.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
methyl (1S,10S,12S,13E,18R)-13-ethylidene-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate	138964044	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(CO)C(=O)OC	352.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
methyl (1S,10S,12S,13E,18R)-13-ethylidene-18-[(3,4,5-trimethoxybenzoyl)oxymethyl]-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate	131636676	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=C3C2CC1C4(COC(=O)C6=CC(=C(C(=C6)OC)OC)OC)C(=O)OC	546.60	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
methyl (1S,10S,12S,13S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate	163185464	Click to see CC=C1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
Methyl 15-ethyl-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate	163006423	Click to see CCC1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC	354.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
Methyl 15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate	162950834	Click to see CC=C1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC	352.40	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
> Alkaloids and derivatives / Yohimbine alkaloids
16-epi-Alstovenine	66577094	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/0031-9422(81)84049-6
16-epi-Venenatine	66577093	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/0031-9422(81)84049-6
Alstovenine	199742	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6 https://doi.org/10.1016/0031-9422(81)84049-6
methyl (1R,15S,18R,19S,20R)-18-hydroxy-8-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate	163000864	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6
methyl (1S,15S,18R,19S,20R)-18-hydroxy-8-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate	163000865	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6
Methyl 17-hydroxy-9-methoxyyohimban-16-carboxylate	433868	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/0031-9422(81)84049-6
Reserpine	5770	Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	608.70	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6
Venenatine	73061	Click to see COC1=CC=CC2=C1C3=C(N2)C4CC5C(CCC(C5C(=O)OC)O)CN4CC3	384.50	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6 https://doi.org/10.1016/0031-9422(81)84049-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0040-4020(01)98382-6
> Organoheterocyclic compounds / Diazaspirononane derivatives
methyl (1S,2R,7S,11S,12R,17S)-12-[(1S)-1-hydroxyethyl]-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-3,5,9-triene-10-carboxylate	162880428	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5C4C=CC=C5OC)C(=O)OC)O	372.50	unknown	https://doi.org/10.1016/0031-9422(82)83125-7
Methyl 12-(1-hydroxyethyl)-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-3,5,9-triene-10-carboxylate	162880427	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5C4C=CC=C5OC)C(=O)OC)O	372.50	unknown	https://doi.org/10.1016/0031-9422(82)83125-7
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
5-Methoxy-2,3,4,9-tetrahydropyrido[3,4-b]indol-1-one	13434113	Click to see COC1=CC=CC2=C1C3=C(N2)C(=O)NCC3	216.24	unknown	https://doi.org/10.1016/0031-9422(82)83125-7
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(2-Hydroxyethoxy)-6-methoxychromen-2-one	85800492	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OCCO	236.22	unknown	https://doi.org/10.1016/0031-9422(82)85212-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
5,6,7-Trimethoxy-3',4'-methylenedioxyisoflavone	21723648	Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC4=C(C=C3)OCO4)OC)OC	356.30	unknown	https://doi.org/10.1016/0031-9422(82)85212-6

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Alstonia venenata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top