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Andrographis affinis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644009260d2ae691738906
Scientific name Andrographis affinis
Authority Nees
First published in Pl. Asiat. Rar. 3: 116 (1832)

Description Top

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Synonyms Top

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Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000534034
Tropicos 100288350
KEW urn:lsid:ipni.org:names:45202-1
The Plant List kew-2637037
Open Tree Of Life 6075802
NCBI Taxonomy 2566155
IPNI 45202-1
iNaturalist 1124398
GBIF 3769619

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)!
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Title Authors Publication Released IDs
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
New 2'-oxygenated flavonoids from Andrographis affinis. Bhaskar Reddy MV, Kishore PH, Rao CV, Gunasekar D, Caux C, Bodo B J Nat Prod 01-Feb-2003
doi:10.1021/NP020331K
PMID:12608871

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 / Terpene lactones / Diterpene lactones
14-Deoxy-11,12-didehydroandrographolide 5708351 Click to see CC12CCC(C(C1CCC(=C)C2C=CC3=CCOC3=O)(C)CO)O 332.40 unknown https://doi.org/10.1021/NP020331K
19-Hydroxy-8(17),13-labdadien-16,15-olide 45934420 Click to see CC1(CCCC2(C1CCC(=C)C2CCC3=CCOC3=O)C)CO 318.40 unknown https://doi.org/10.1021/NP020331K
4-[2-[6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 4262071 Click to see CC12CCC(C(C1CCC(=C)C2C=CC3=CCOC3=O)(C)CO)O 332.40 unknown https://doi.org/10.1021/NP020331K
Andrograpanin 11666871 Click to see CC1(CCCC2(C1CCC(=C)C2CCC3=CCOC3=O)C)CO 318.40 unknown https://doi.org/10.1021/NP020331K
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-(2,3,4-trimethoxyphenyl)-2,3-dihydrochromen-4-one 637184 Click to see COC1=C(C(=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 374.40 unknown https://doi.org/10.1021/NP020331K
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 11081450 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC=C2C3=CC(=O)C4=C(C=C(C=C4O3)OC)O)O)O)O 488.40 unknown https://doi.org/10.1021/NP020331K
[3,4,5-Trihydroxy-6-[2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 74977416 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC=C2C3=CC(=O)C4=C(C=C(C=C4O3)OC)O)O)O)O 488.40 unknown https://doi.org/10.1021/NP020331K
5,7,2',3',4'-Pentamethoxyflavanone 21573556 Click to see COC1=C(C(=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 374.40 unknown https://doi.org/10.1021/NP020331K
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(S)-5-Hydroxy-7,8-dimethoxy-2-phenylchroman-4-one 13963771 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1021/NP020331K
5-Hydroxy-7,8-dimethoxyflavanone 13963770 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)O)OC 300.30 unknown https://doi.org/10.1021/NP020331K
5-Hydroxy-7,8-dimethoxyflavone 188316 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)OC 298.29 unknown https://doi.org/10.1021/NP020331K
5-Hydroxy-7,8,2',5'tetramethoxyflavone 10948318 Click to see COC1=CC(=C(C=C1)OC)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC 358.30 unknown https://doi.org/10.1021/NP020331K
Andrographin 5318506 Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC 328.30 unknown https://doi.org/10.1021/NP020331K
Skullcapflavone I 5320399 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3O)OC 314.29 unknown https://doi.org/10.1021/NP020331K

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