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Internal ID UUID64404b8e73907317124062
Scientific name Marsdenia tinctoria
Authority R.Br.
First published in Asclepiadeae : 17 (1810)

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Synonyms Top

Scientific name Authority First published in
Marsdenia monostachya Wall. ex Hook.f. Fl. Brit. India 4: 34 (1883)
Marsdenia akkar Blanco Fl. Filip. : 118 (1837)
Marsdenia tagudinia Blanco Fl. Filip. : 121 (1837)
Asclepias tinctoria (R.Br.) Roxb. Fl. Ind. ed. 1832 , 2: 43 (1832)
Cynanchum tingens Buch.-Ham. ex Hook.f. Fl. Brit. India 4: 34 (1883)
Pergularia parviflora Blume Bijdr. Fl. Ned. Ind. : 1056 (1826)
Pergularia tinctoria (R.Br.) Spreng. Syst. Veg. 1: 844 (1824)
Marsdenia globifera Tsiang Sunyatsenia 3: 199 (1936)
Marsdenia tinctoria var. tomentosa Masam. ex Tsiang & P.T.Li Acta Phytotax. Sin. 12: 117 (1974)
Marsdenia tinctoria var. brevis Costantin Fl. Indo-Chine 4: 94. 1912

Common names Top

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Language Common/alternative name
Japanese 染物蔓
Japanese ソメモノカズラ
Malay pokok akar tarum
Malay akar tarum
Thai ครามเถา
Chinese 蓝叶藤
Chinese 球花牛奶菜
Chinese 篮叶藤果
Chinese 絨毛芙蓉蘭
Chinese 肖牛耳藤
Chinese 芙蓉兰
Chinese 短序蓝叶藤
Chinese 绒毛芙蓉兰

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001102203
Tropicos 2601803
KEW urn:lsid:ipni.org:names:99325-1
The Plant List tro-2601803
Open Tree Of Life 5784568
NCBI Taxonomy 2072778
IPNI 99326-1
iNaturalist 703025
GBIF 7312032
USDA GRIN 464434

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
“Purplish Blue” or “Greenish Grey”? Indigo Qualities and Extraction Yields from Six Species Hartl A, Polleichtner A, Novak J Plants (Basel) 22-Mar-2024
PMCID:PMC11013892
doi:10.3390/plants13070918
PMID:38611450
Ethnomedicinal plants in Champadevi rural municipality, Okhaldhunga district, Nepal Karki D, Khadka D, Kunwar RM, Aryal PC, Paudel HR, Bhatta S, Shi S J Ethnobiol Ethnomed 11-Dec-2023
PMCID:PMC10712033
doi:10.1186/s13002-023-00627-y
PMID:38072922
Selected flavonoids exhibit antibiofilm and antibacterial effects against Vibrio by disrupting membrane integrity, virulence and metabolic activities Faleye OS, Lee JH, Lee J Biofilm 07-Nov-2023
PMCID:PMC10681883
doi:10.1016/j.bioflm.2023.100165
PMID:38034415
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Seasonal variations in group leaf characteristics in species with red young leaves Zhang TJ, Tian XS, Liu XT, Huang XD, Peng CL Sci Rep 11-Nov-2019
PMCID:PMC6848096
doi:10.1038/s41598-019-52753-x
PMID:31712569
Effect of different physico-chemical parameters for natural indigo production during fermentation of Indigofera plant biomass Dutta S, Roychoudhary S, Sarangi BK 3 Biotech 16-Sep-2017
PMCID:PMC5602782
doi:10.1007/s13205-017-0923-2
PMID:28955619
Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP J Ethnobiol Ethnomed 03-May-2016
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597
A triterpene from Marsdenia globifera Qiu Sheng-Xiang, Gong Yong, H.T.A. Cheung Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80034-X
[Study on the constituents of Marsdenia tinctoria var. tomentosa Masamune (author's transl)]. Ito K, Lai J Yakugaku Zasshi 01-Sep-1978
doi:10.1248/YAKUSHI1947.98.9_1285
PMID:731402

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bS,8aR,11R,12S,12aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one 5318252 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
[(1S,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] hexadecanoate 162847784 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1248/YAKUSHI1947.98.9_1285
alpha-Amyrenone 12306155 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Sambuculin a 14486636 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1248/YAKUSHI1947.98.9_1285
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(1S)-1-[(3S,8S,9R,10R,12R,13R,14R,17S)-3,8,12,14,17-pentahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]ethyl] (E)-3-phenylprop-2-enoate 14411663 Click to see CC(C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)O)C)O)O)OC(=O)C=CC5=CC=CC=C5 512.60 unknown https://doi.org/10.1016/0031-9422(91)80034-X
14beta-Pregn-5-en-20-one, 3beta,8,12beta,14-tetrahydroxy- 22213147 Click to see CC(=O)C1CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)O)C)O 364.50 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Gagaminin 44575627 Click to see CC(C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C=CC5=CC=CC=C5)C)O)O)OC(=O)C6=CN=CC=C6 617.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Gymnemarsgenin 101683294 Click to see CC(C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C=CC5=CC=CC=C5)C)O)O)OC(=O)C6=CC=CC=C6 616.70 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Penupogenin 56841085 Click to see CC(C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C=CC5=CC=CC=C5)C)O)O)O 512.60 unknown https://doi.org/10.1016/0031-9422(91)80034-X
Sarcostin 46173994 Click to see CC(C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)O)C)O)O)O 382.50 unknown https://doi.org/10.1016/0031-9422(91)80034-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1248/YAKUSHI1947.98.9_1285

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