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Andrographis alata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644009261ce39279451596
Scientific name Andrographis alata
Authority (Vahl) Nees
First published in Prodr. 11: 516 (1847)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Justicia alata Vahl Enum. Pl. 1: 139 (1804)

Common names Top

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Language Common/alternative name
Tamil சிறியா நங்கை
Tamil ''andrographis alata''

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-0000534035
Tropicos 100288351
KEW urn:lsid:ipni.org:names:45203-1
The Plant List kew-2637038
Open Tree Of Life 5921416
Observations.org 265475
NCBI Taxonomy 1752146
IPNI 45203-1
iNaturalist 1095227
GBIF 3769612
Elurikkus 410136

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
Role of Nanoparticle-Conjugates and Nanotheranostics in Abrogating Oxidative Stress and Ameliorating Neuroinflammation Patel TA, Kevadiya BD, Bajwa N, Singh PA, Zheng H, Kirabo A, Li YL, Patel KP Antioxidants (Basel) 18-Oct-2023
PMCID:PMC10604131
doi:10.3390/antiox12101877
PMID:37891956
Micropropagation of Andrographis producta through axillary and adventitious shoot regeneration Kadapatti SS, Murthy HN J Genet Eng Biotechnol 01-Nov-2022
PMCID:PMC9626720
doi:10.1186/s43141-022-00438-w
PMID:36318363
Whole transcriptome analysis identifies full-length genes for neoandrographolide biosynthesis from Andrographis alata, an alternate source for antiviral compounds Tanuja, Parani M Gene 19-Oct-2022
PMCID:PMC9578972
doi:10.1016/j.gene.2022.146981
PMID:36270458
Rapid plant regeneration, analysis of genetic fidelity, and neoandrographolide content of micropropagated plants of Andrographis alata (Vahl) Nees Kadapatti SS, Murthy HN J Genet Eng Biotechnol 26-Jan-2021
PMCID:PMC7835653
doi:10.1186/s43141-021-00122-5
PMID:33496903
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
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
Acylated 5,7,2',6'-oxygenated flavone glycosides from Andrographis alata. Das B, Ramu R, Rao YK, Reddy MR, Harish H, Reddy VS, Ramakrishna KV Phytochemistry 01-May-2006
doi:10.1016/J.PHYTOCHEM.2006.03.003
PMID:16624351
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
A flavone glycoside from Andrographis alata. Damu AG, Jayaprakasam B, Rao KV, Gunasekar D Phytochemistry 20-Nov-1998
doi:10.1016/S0031-9422(98)00342-2
PMID:11711108
A new flavone 2'-glucoside from Andrographis alata. Damu AG, Jayaprakasam B, Gunasekar D J Asian Nat Prod Res 01-Jan-1998
doi:10.1080/10286029808039855
PMID:11261214
NOMENCLATURAL CONFUSION OF SOME SPECIES OF ANDROGRAPHIS WALL Balu S, Alagesaboopathi C Anc Sci Life 01-Jan-1995
PMCID:PMC3331236
PMID:22556690
ANTI-INFLAMMATORY ACTIVITIES OF SOME SPECIES OF ANDROGRAPHIS WALL. (ACANTHACEAE) Balu S, Alagesaboopathi C Anc Sci Life 01-Jul-1993
PMCID:PMC3336537
PMID:22556645
ANTIPYRETIC ACTIVITIES OF SOME SPECIES OF ANDROGRAPHIS WALL Balu S, Boopathi CA, Elango V Anc Sci Life 01-Jan-1993
PMCID:PMC3336550
PMID:22556619

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 / Saccharolipids
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl (E)-but-2-enoate 102187175 Click to see 530.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[3,4,5-Trihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl but-2-enoate 162964752 Click to see 530.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[2-(2,6-dihydroxyphenyl)-7-methoxy-4-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163078270 Click to see 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[6-[2-(2,6-Dihydroxyphenyl)-7-methoxy-4-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163078269 Click to see 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
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 446.40 unknown https://doi.org/10.1016/S0031-9422(98)00342-2
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/10.1016/S0031-9422(98)00342-2
2-(2-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977415 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(98)00342-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
[(2R,3R,4S,5R,6S)-4-acetyloxy-3,5-dihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 102187173 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 163037014 Click to see 488.40 unknown https://doi.org/10.1021/NP020331K
[(2R,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 102187172 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]-6-(hydroxymethyl)oxan-3-yl] acetate 102187174 Click to see 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[4-Acetyloxy-3,5-dihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 162869805 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[4,5-Dihydroxy-2-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]-6-(hydroxymethyl)oxan-3-yl] acetate 163035733 Click to see 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
[5-Acetyloxy-3,4-dihydroxy-6-[3-hydroxy-2-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenoxy]oxan-2-yl]methyl acetate 163002660 Click to see 546.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
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/10.1016/J.PHYTOCHEM.2006.03.003
5-hydroxy-2-[2-hydroxy-6-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 162994507 Click to see 462.40 unknown https://doi.org/10.1080/10286029808039855
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 74977418 Click to see 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.003
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(98)00342-2

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