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Indigofera hebepetala

Indigofera hebepetala - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fdbcb85c2b789984262
Scientific name Indigofera hebepetala
Authority Benth. ex Baker
First published in J.D.Hooker, Fl. Brit. India2: 101 (1876)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anil hebepetala (Benth. ex Baker) Kuntze Revis. Gen. Pl.2: 939 (1891)

Common names Top

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Language Common/alternative name
Chinese 毛瓣木蓝

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Indigofera hebepetala var. glabra Ali Bot. Not.111: 572 (1958)
Indigofera hebepetala var. hebepetala Baker Unknown

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
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000197534
Tropicos 13020805
KEW urn:lsid:ipni.org:names:499436-1
The Plant List ild-44075
PFAF Indigofera hebepetala
Open Tree Of Life 669091
NCBI Taxonomy 198879
IPNI 499436-1
GBIF 2972182
EPPO INDHE
EOL 648380
USDA GRIN 20016

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
Environmental variables drive plant species composition and distribution in the moist temperate forests of Northwestern Himalaya, Pakistan Rahman IU, Hart RE, Ijaz F, Afzal A, Iqbal Z, Calixto ES, Abd_Allah EF, Alqarawi AA, Hashem A, Al-Arjani AB, Kausar R, Haq SM PLoS One 24-Feb-2022
PMCID:PMC8870539
doi:10.1371/journal.pone.0260687
PMID:35202409
Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES Plants (Basel) 28-Dec-2021
PMCID:PMC8747448
doi:10.3390/plants11010087
PMID:35009089
Species Distribution Pattern and Their Contribution in Plant Community Assembly in Response to Ecological Gradients of the Ecotonal Zone in the Himalayan Region Rahman IU, Afzal A, Iqbal Z, Hashem A, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Abdalla M, Calixto ES, Sakhi S, Ali N, Bussmann RW Plants (Basel) 04-Nov-2021
PMCID:PMC8623140
doi:10.3390/plants10112372
PMID:34834735
Wild plants used by the Lhoba people in Douyu Village, characterized by high mountains and valleys, in southeastern Tibet, China Chen WY, Yang T, Yang J, Qiu ZC, Ding XY, Wang YH, Wang YH J Ethnobiol Ethnomed 23-Jul-2021
PMCID:PMC8305498
doi:10.1186/s13002-021-00472-x
PMID:34301287
Antimicrobial Activity of Indigofera suffruticosa Leite SP, Vieira JR, de Medeiros PL, Leite RM, de Menezes Lima VL, Xavier HS, de Oliveira Lima E Evid Based Complement Alternat Med 05-Apr-2006
PMCID:PMC1475935
doi:10.1093/ecam/nel010
PMID:16786057
Flavonoid glycosides from Indigofera hebepetala Aurangzeb Hasan, Mohammed Farman, Iftikhar Ahmed Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90552-1
Two flavonol triglycosides from flowers of Indigofera hebepetala. Hasan A, Ahmad I, Khan MA, Chudhary MI Phytochemistry 01-Nov-1996
doi:10.1016/S0031-9422(96)00416-5
PMID:8987878

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 / Flavonoid-7-O-glycosides
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one 13940823 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 54431865 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
5-Hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 14334872 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
7-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163009360 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(O5)CO)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 726.60 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
7-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 102444978 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(O5)CO)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O 726.60 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
7-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102444979 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(O5)CO)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 726.60 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 163041268 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(O5)CO)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O 726.60 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 74978102 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(O5)CO)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 726.60 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
kaempferol 3-O-alpha-L-arabinopyranosyl-7-O-alpha-L-rhamnopyranoside 57401109 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
Kaempferol 3-rhamnoside 7-xyloside 14334866 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(96)00416-5
Kaempferol 7-alloside 44258920 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)90552-1
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(96)00416-5

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