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Andrographis stenophylla

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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 UUID64400928369e1449757484
Scientific name Andrographis stenophylla
Authority C.B.Clarke
First published in Fl. Brit. India 4: 503 (1884)

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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No germination or propagation data was added yet.

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-0000534079
Tropicos 100288377
KEW urn:lsid:ipni.org:names:45232-1
The Plant List kew-2637078
Open Tree Of Life 6075822
IPNI 45232-1
iNaturalist 1124407
GBIF 3769334

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)!
Title Authors Publication Released IDs
Flavonoids from Andrographis viscosula. Yerra Koteswara Rao, Amooru Gangaiah Damu, Alahari Janardhan Rao, Shanmuganathan Venkatesan, Ping‐Chung Kuo, Chunduri Venkata Rao, Tian‐Shung Wu Wiley 15-Apr-2004
doi:10.1002/CHIN.200419204
Flavonoids from Andrographis viscosula. Rao YK, Damu AG, Rao AJ, Venkatesan S, Kuo PC, Rao CV, Wu TS Chem Pharm Bull (Tokyo) 01-Dec-2003
doi:10.1248/CPB.51.1374
PMID:14646312
Flavones from Andrographis viscosula. Rao YK, Harikishore P, Rao CV, Gunasekar D, Blond A, Bodo B Phytochemistry 01-Dec-2002
doi:10.1016/S0031-9422(02)00389-8
PMID:12453519

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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(2-hydroxyphenyl)-7-methoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 100929637 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=CC=C4O 446.40 unknown https://doi.org/10.1248/CPB.51.1374
2-(2-hydroxyphenyl)-7-methoxy-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163090635 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=CC=C4O 446.40 unknown https://doi.org/10.1248/CPB.51.1374
2-(2-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977415 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=CC=C4O 446.40 unknown https://doi.org/10.1248/CPB.51.1374
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-Hydroxy-7,2',3'-trimethoxyflavanone 9996718 Click to see COC1=CC=CC(=C1OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 330.30 unknown https://doi.org/10.1248/CPB.51.1374
2-(2,3-Dimethoxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 85087212 Click to see COC1=CC=CC(=C1OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 330.30 unknown https://doi.org/10.1248/CPB.51.1374
2-(2,5-Dimethoxyphenyl)-7-methoxychromen-4-one 11255399 Click to see COC1=CC(=C(C=C1)OC)C2=CC(=O)C3=C(O2)C=C(C=C3)OC 312.30 unknown https://doi.org/10.1248/CPB.51.1374
4H-1-Benzopyran-4-one, 2-(2,3-dimethoxyphenyl)-5,7-dimethoxy- 11772234 Click to see COC1=CC=CC(=C1OC)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 342.30 unknown https://doi.org/10.1248/CPB.51.1374
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 101262883 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.51.1374
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 74977418 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.51.1374
5-hydroxy-7-methoxy-2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 9496891 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(02)00389-8
https://doi.org/10.1248/CPB.51.1374
5-Hydroxy-7-methoxy-2-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 6018900 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.51.1374
https://doi.org/10.1016/S0031-9422(02)00389-8
5-Hydroxy-7,2'-dimethoxyflavone 10913533 Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1248/CPB.51.1374
5,2',6'-Trihydroxy-7-methoxyflavone 10946502 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=C(C=CC=C3O)O)O 300.26 unknown https://doi.org/10.1248/CPB.51.1374
https://doi.org/10.1016/S0031-9422(02)00389-8
5,7,2'-Trimethoxyflavone 5322103 Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown https://doi.org/10.1016/S0031-9422(02)00389-8
https://doi.org/10.1248/CPB.51.1374
5,7,2',4',6'-Pentamethoxyflavone 5320479 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=C(C=C(C=C3OC)OC)OC 372.40 unknown https://doi.org/10.1248/CPB.51.1374
https://doi.org/10.1016/S0031-9422(02)00389-8
Echioidin 44257608 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1002/CHIN.200419204
Echioidinin 15559079 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(02)00389-8
https://doi.org/10.1002/CHIN.200419204
https://doi.org/10.1248/CPB.51.1374

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