Andrographis lineata - Unknown
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Internal ID UUID6440092719926062020394
Scientific name Andrographis lineata
Authority Nees
First published in Pl. Asiat. Rar. 3: 116 (1832)

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Language Common/alternative name
Tamil பெரியா நங்கை

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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-0000534054
Tropicos 100288361
KEW urn:lsid:ipni.org:names:45218-1
The Plant List kew-2637055
Open Tree Of Life 1071632
NCBI Taxonomy 592315
IPNI 45218-1
iNaturalist 1102151
GBIF 3769482
CMAUP NPO18156

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
Anti-Cancer Agent: The Labdane Diterpenoid-Andrographolide Tundis R, Patra JK, Bonesi M, Das S, Nath R, Das Talukdar A, Das G, Loizzo MR Plants (Basel) 12-May-2023
PMCID:PMC10221142
doi:10.3390/plants12101969
PMID:37653887
Differential Gene Expression and Withanolides Biosynthesis During in vitro and ex vitro Growth of Withania somnifera (L.) Dunal Thorat SA, Kaniyassery A, Poojari P, Rangel M, Tantry S, Kiran KR, Joshi MB, Rai PS, Botha AM, Muthusamy A Front Plant Sci 14-Jun-2022
PMCID:PMC9237602
doi:10.3389/fpls.2022.917770
PMID:35774803
Integrative Alternative Tactics for Ixodid Control Showler AT, Saelao P Insects 18-Mar-2022
PMCID:PMC8948879
doi:10.3390/insects13030302
PMID:35323601
Production of Flavonoids in Callus Cultures of Sophora flavescens Aiton Park JS, Seong ZK, Kim MS, Ha JH, Moon KB, Lee HJ, Lee HK, Jeon JH, Park SU, Kim HS Plants (Basel) 28-May-2020
PMCID:PMC7356026
doi:10.3390/plants9060688
PMID:32481711
Termites and Chinese agricultural system: applications and advances in integrated termite management and chemical control Ahmad F, Fouad H, Liang S, Hu Y, Mo J Insect Sci 15-Oct-2019
PMCID:PMC7818233
doi:10.1111/1744-7917.12726
PMID:31529680
Multi-Target β-Protease Inhibitors from Andrographis paniculata: In Silico and In Vitro Studies Panche AN, Chandra S, Diwan A Plants (Basel) 17-Jul-2019
PMCID:PMC6681301
doi:10.3390/plants8070231
PMID:31319560
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
In Vitro Production of Echioidinin, 7-O-Methywogonin from Callus Cultures of Andrographis lineata and Their Cytotoxicity on Cancer Cells Mohammed A, Chiruvella KK, Rao YK, Geethangili M, Raghavan SC, Ghanta RG PLoS One 21-Oct-2015
PMCID:PMC4619555
doi:10.1371/journal.pone.0141154
PMID:26488879
Traditional Use of Plants Against Snakebite in Indian Subcontinent: A Review of the Recent Literature Dey A, De JN Afr J Tradit Complement Altern Med 02-Oct-2011
PMCID:PMC3746536
doi:10.4314/ajtcam.v9i1.20
PMID:23983332
Efficacy of indigenous plant extracts on the malaria vector Anopheles subpictus Grassi (Diptera: Culicidae) Elango G, Zahir AA, Bagavan A, Kamaraj C, Rajakumar G, Santhoshkumar T, Marimuthu S, Rahuman AA Indian J Med Res 01-Sep-2011
PMCID:PMC3193720
PMID:21985822
Ethnobotanical investigations among tribes in Madurai District of Tamil Nadu (India) Ignacimuthu S, Ayyanar M, Sivaraman K S J Ethnobiol Ethnomed 11-May-2006
PMCID:PMC1475842
doi:10.1186/1746-4269-2-25
PMID:16689985
Flavonoids from Andrographis lineata. Kishore PH, Reddy MV, Reddy MK, Gunasekar D, Caux C, Bodo B Phytochemistry 01-Jun-2003
doi:10.1016/S0031-9422(02)00702-1
PMID:12770598

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2S,3R,4R,4aS,10bR)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 471287 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
taepeenin D 11703693 Click to see CC1=C2CC(C3C(C2=CC4=C1C=CO4)(CCCC3(C)C(=O)OC)C)OC(=O)C 384.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4R)-7alpha-[(4S)-4,7,11bbeta-Trimethyl-4alpha-(methoxycarbonyl)-1,2,3,4,4aalpha,5,6,11b-octahydrophenanthro[3,2-b]furan-9-yl]-4,7beta,11balpha-trimethyl-1,2,3,4,4abeta,5,6,6aalpha,7,11,11abeta,11b-dodecahydrophenanthro[3,2-b]furan-4beta-carboxylic acid methyl ester 49780661 Click to see CC1=C2CCC3C(C2=CC4=C1C=C(O4)C5(C6CCC7C(C6CC8=C5C=CO8)(CCCC7(C)C(=O)OC)C)C)(CCCC3(C)C(=O)OC)C 654.90 unknown via CMAUP database
(5alpha,8beta,10beta,14alpha)-Cassa-13(15)-ene-12beta,16-diol 49780445 Click to see CC1C2CCC3C(CCCC3(C2CC(C1=CCO)O)C)(C)C 306.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pterocarpol 12314741 Click to see CC12CCC(CC1C(=C)CC(C2)O)C(C)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
3-{2-[2,5,5-tris(hydroxymethyl)-8a-methyldecahydro-1-naphthalenyl]ethyl}-2(5H)-furanone 76326826 Click to see CC12CCCC(C1CCC(C2CCC3=CCOC3=O)CO)(CO)CO 352.50 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
4-[2-[2,5,5-tris(hydroxymethyl)-8a-methyl-1,2,3,4,4a,6,7,8-octahydronaphthalen-1-yl]ethyl]-2H-furan-5-one 4070411 Click to see CC12CCCC(C1CCC(C2CCC3=CCOC3=O)CO)(CO)CO 352.50 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(5alpha,8beta,10beta,13R,14R,15R)-12beta,16-Diacetoxy-13-methyl-17-nor-14,15-cyclocassane 49780446 Click to see CC(=O)OCC1C2C1(C(CC3C2CCC4C3(CCCC4(C)C)C)OC(=O)C)C 390.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
1-[2-(Hydroxymethyl)-2-propenyl]-3-methoxydibenzofuran-2,7-diol 49780662 Click to see COC1=C(C(=C2C3=C(C=C(C=C3)O)OC2=C1)CC(=C)CO)O 300.30 unknown via CMAUP database
1-[2-(Hydroxymethyl)-2-propenyl]-3,7-dimethoxydibenzofuran-2-ol 49780663 Click to see COC1=CC2=C(C=C1)C3=C(C(=C(C=C3O2)OC)O)CC(=C)CO 314.30 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(5alpha,10beta)-8beta-Hydroxy-12,16-epoxycassa-12,14(17),15-triene-18-oic acid methyl ester 49780444 Click to see CC12CCCC(C1CCC3(C2CC4=C(C3=C)C=CO4)O)(C)C(=O)OC 344.40 unknown via CMAUP database
Nortaepeenin A 11587964 Click to see CC12CCCC(C1CCC3C2CC4=C(C3=O)C=CO4)(C)C(=O)OC 330.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Tetracosyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 78385378 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 516.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2',3',4',5,7-Pentamethoxyflavone 373146 Click to see COC1=C(C(=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
5-Hydroxy-2-(2-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 73196511 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
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)00702-1
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/10.1016/S0031-9422(02)00702-1
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/10.1016/S0031-9422(02)00702-1
Dihydroechioidinin 15491078 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
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)00702-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2R)-5-hydroxy-7,8-dimethoxy-2-phenyl-2,3-dihydrochromen-4-one 26248801 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/10.1016/S0031-9422(02)00702-1
(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/10.1016/S0031-9422(02)00702-1
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/10.1016/S0031-9422(02)00702-1
5,2'-Dihydroxy-7,8-dimethoxyflavanone 12098358 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3O)C(=C1)O)OC 316.30 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
Scullcapflavone 85434272 Click to see COC1=C(C2=C(C(=O)CC(O2)C3=CC=CC=C3O)C(=C1)O)OC 316.30 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
Serpyllin 12315479 Click to see COC1=C(C(=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)OC)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
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/10.1016/S0031-9422(02)00702-1
> Phenylpropanoids and polyketides / Homoisoflavonoids
Bonducellin 14079439 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
Intricatinol 6439175 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3O)O 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(2-methoxyphenyl)prop-2-en-1-one 4309692 Click to see COC1=CC=CC=C1C=CC(=O)C2=C(C=C(C=C2OC)OC)O 314.30 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
2'-Hydroxy-2,4',6'-trimethoxychalcone 637261 Click to see COC1=CC=CC=C1C=CC(=O)C2=C(C=C(C=C2OC)OC)O 314.30 unknown https://doi.org/10.1016/S0031-9422(02)00702-1
> Phenylpropanoids and polyketides / Stilbenes
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database

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