Andrographis echioides - Unknown
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Internal ID UUID644009267490e358480777
Scientific name Andrographis echioides
Authority Nees
First published in Pl. Asiat. Rar. 3: 117 (1832)

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Synonyms Top

Scientific name Authority First published in
Justicia echioides L. Sp. Pl. : 16 (1753)
Neesiella echioides (L.) Sreem. Phytologia 15: 271 (1967)
Eriathera lobelioides Nees Pl. Asiat. Rar. 3: 115 (1832)
Indoneesiella echioides (L.) Sreem. Phytologia 16: 466 (1968)
Erianthera echioides (L.) M.R.Almeida Fl. Maharashtra 4A: 40. 2003
Justicia echinoides L. 1: 16 16 1753
Erianthera lobelioides Nees Pl. Asiat. Rar. 3: 115 (1832)

Common names Top

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Language Common/alternative name
English false waterwillow
Malayalam ഗോപുരംതാങ്ങി

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
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Sri Lanka
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000534042
USDA Plants ANEC
Tropicos 100004
KEW urn:lsid:ipni.org:names:45208-1
The Plant List kew-2637044
PaleoBotany 110457
Open Tree Of Life 516626
NCBI Taxonomy 526786
IPNI 45208-1
iNaturalist 626166
GBIF 3173179
EPPO ADGEC
EOL 596695
USDA GRIN 447803

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
An efficient in vitro organogenesis protocol for the endangered relic tree species Bretschneidera sinensis and genetic fidelity assessment using DNA markers Yan X, Zheng K, Li P, Zhong X, Zhu Z, Zhou H, Zhu M Front Plant Sci 10-Apr-2024
PMCID:PMC11039884
doi:10.3389/fpls.2024.1259925
PMID:38660444
Polysaccharides from Spirulina platensis (PSP): promising biostimulants for the green synthesis of silver nanoparticles and their potential application in the treatment of cancer tumors Al-Badwy AH, Khalil AM, Bashal AH, Kebeish R Microb Cell Fact 05-Dec-2023
PMCID:PMC10699016
doi:10.1186/s12934-023-02257-1
PMID:38053190
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Biosynthesis of Functional Silver Nanoparticles Using Callus and Hairy Root Cultures of Aristolochia manshuriensis Yugay YA, Sorokina MR, Grigorchuk VP, Rusapetova TV, Silant’ev VE, Egorova AE, Adedibu PA, Kudinova OD, Vasyutkina EA, Ivanov VV, Karabtsov AA, Mashtalyar DV, Degtyarenko AI, Grishchenko OV, Kumeiko VV, Bulgakov VP, Shkryl YN J Funct Biomater 01-Sep-2023
PMCID:PMC10532211
doi:10.3390/jfb14090451
PMID:37754865
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
HPTLC and GC–MS finger-printing of two potential multifunctional siddha tailams: Mathan and maha megarajanga tailam Senthilnathan S, Jayaraman S, Priya Veeraraghavan V, Masood Khan J, Ahmed MZ, Ahmad A, Gnanamani A Saudi J Biol Sci 01-Jun-2023
PMCID:PMC10276281
doi:10.1016/j.sjbs.2023.103700
PMID:37333677
Exploring the biological application of Penicillium fimorum-derived silver nanoparticles: In vitro physicochemical, antifungal, biofilm inhibitory, antioxidant, anticoagulant, and thrombolytic performance Barabadi H, Mobaraki K, Jounaki K, Sadeghian-Abadi S, Vahidi H, Jahani R, Noqani H, Hosseini O, Ashouri F, Amidi S Heliyon 01-Jun-2023
PMCID:PMC10258451
doi:10.1016/j.heliyon.2023.e16853
PMID:37313153
Anticancer potential of biologically synthesized silver nanoparticles using Lantana camara leaf extract Hublikar LV, Ganachari SV, Patil VB, Nandi S, Honnad A Prog Biomater 24-Apr-2023
PMCID:PMC10154448
doi:10.1007/s40204-023-00219-9
PMID:37093445
HMC Ameliorates Hyperglycemia via Acting PI3K/AKT Pathway and Improving FOXO1 Pathway in ob/ob Mice Yoo J, Park JE, Han JS Nutrients 22-Apr-2023
PMCID:PMC10181050
doi:10.3390/nu15092023
PMID:37432173
Applications of Green Synthesized Metal Nanoparticles — a Review Vijayaram S, Razafindralambo H, Sun YZ, Vasantharaj S, Ghafarifarsani H, Hoseinifar SH, Raeeszadeh M Biol Trace Elem Res 13-Apr-2023
PMCID:PMC10097525
doi:10.1007/s12011-023-03645-9
PMID:37046039
Novel archetype in cancer therapeutics: exploring prospective of phytonanocarriers Yadav N, Singh D, Rawat M, Sangwan N 3 Biotech 15-Oct-2022
PMCID:PMC9569404
doi:10.1007/s13205-022-03372-3
PMID:36276448
In vitro antioxidant and anti-diabetic analysis of Andrographis echioides and Andrographis paniculata ethanol extract Shreya Reddy CS, Ramalingam GD, Selvaraj J, Jothi Priya A Bioinformation 30-Apr-2022
PMCID:PMC9997502
doi:10.6026/97320630018337
PMID:36909701
In vitro anti-inflammatory and wound healing properties of Andrographis echioides and Andrographis paniculata Selvaraj K, Gayatri Devi R, Selvaraj J, Jothi Priya A Bioinformation 30-Apr-2022
PMCID:PMC9997496
doi:10.6026/97320630018331
PMID:36909694
The Potential Application of Green-Synthesized Metal Nanoparticles in Dentistry: A Comprehensive Review Yazdanian M, Rostamzadeh P, Rahbar M, Alam M, Abbasi K, Tahmasebi E, Tebyaniyan H, Ranjbar R, Seifalian A, Yazdanian A Bioinorg Chem Appl 03-Mar-2022
PMCID:PMC8913069
doi:10.1155/2022/2311910
PMID:35281331

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
(E)-1-[2-hydroxy-4-methoxy-6-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(2-hydroxyphenyl)prop-2-en-1-one 163067916 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3O)O 448.40 unknown https://doi.org/10.1080/10286020108042837
Androechin 42607586 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3O)O 448.40 unknown https://doi.org/10.1080/10286020108042837
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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(99)00295-2
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/S0040-4020(01)96987-X
https://doi.org/10.1016/S0031-9422(99)00295-2
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(99)00295-2
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(99)00295-2
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/10.1016/S0031-9422(99)00295-2
Echioidinin 15559079 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3O)O 284.26 unknown https://doi.org/10.1016/0040-4020(67)85020-8
https://doi.org/10.1016/S0031-9422(99)00295-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-hydroxy-7,8-dimethoxy-2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 100984956 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)OC 476.40 unknown https://doi.org/10.1016/S0031-9422(99)00295-2
5-Hydroxy-7,8-dimethoxy-2-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 74977899 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)OC 476.40 unknown https://doi.org/10.1016/S0031-9422(99)00295-2
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/10.1016/S0031-9422(99)00295-2

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