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Cyathula capitata

Cyathula capitata - 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 UUID6440149ed48cd982149368
Scientific name Cyathula capitata
Authority Moq.
First published in Prodr. 13(2): 329 (1849)

Description Top

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Synonyms Top

Scientific name Authority First published in
Achyranthes hamata H.Lév. & Vaniot Fl. Kouy-Tchéou : 23 (1915)

Common names Top

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Language Common/alternative name
Chinese 白牛膝
Chinese 川牛膝
Chinese 头花杯苋
Chinese 头花杯苋（头花蒽草、川牛膝）
Chinese 麻牛漆
Chinese 麻牛膝
Chinese 头花蒽草
Chinese 頭花杯莧

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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No forms added yet.

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
      • West Himalaya
    • Indo-China
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000631174
Tropicos 50066128
KEW urn:lsid:ipni.org:names:60146-1
The Plant List kew-2749194
Open Tree Of Life 6033812
NCBI Taxonomy 2152776
IPNI 60146-1
iNaturalist 603088
GBIF 5548610
EOL 2873103
USDA GRIN 423373

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
Identification of Active Compounds From Yi Nationality Herbal Formula Wosi Influencing COX-2 and VCAM-1 Signaling Zhang JZ, Chen XY, Wu YJ, Li LM, Huang L, Yin QZ, Luo P, Liu Y Front Pharmacol 09-Nov-2020
PMCID:PMC7797783
doi:10.3389/fphar.2020.568585
PMID:33442381
Comparing and phylogenetic analysis chloroplast genome of three Achyranthes species Xu J, Shen X, Liao B, Xu J, Hou D Sci Rep 02-Jul-2020
PMCID:PMC7331806
doi:10.1038/s41598-020-67679-y
PMID:32616875
The complete chloroplast genome sequence of a traditional Chinese medicine: Achyranthes bidentata (Amaranthaceae) Li ZH, Li XH, Ling LZ, Ai HL, Zhang SD Mitochondrial DNA B Resour 11-Dec-2019
PMCID:PMC7721043
doi:10.1080/23802359.2019.1698362
PMID:33366466
Review of traditional uses, botany, chemistry, pharmacology, pharmacokinetics, and toxicology of Radix Cyathulae Huang Y, Wang S, Liu L, Peng W, Wang J, Song Y, Yuan Q, Yuan X, Wu C Chin Med 30-Apr-2019
PMCID:PMC6492438
doi:10.1186/s13020-019-0237-x
PMID:31068976
Effects of Qi-Fang-Xi-Bi-Granules on Cartilage Morphology and C/ebpα Promoter Methylation in Rats with Knee Osteoarthritis Wang X, Shen P, Tang D, Xu H, Qiu H, Wu T, Gao X Evid Based Complement Alternat Med 28-Jan-2018
PMCID:PMC5833195
doi:10.1155/2018/2074976
PMID:29670657
Ecdysteroid-containing food supplements from Cyanotis arachnoidea on the European market: evidence for spinach product counterfeiting Hunyadi A, Herke I, Lengyel K, Báthori M, Kele Z, Simon A, Tóth G, Szendrei K Sci Rep 08-Dec-2016
PMCID:PMC5144001
doi:10.1038/srep37322
PMID:27929032
Possible Inhibitor from Traditional Chinese Medicine for the β Form of Calcium-Dependent Protein Kinase Type II in the Treatment of Major Depressive Disorder Hung TC, Lee WY, Chen KB, Huang HJ, Chan YC, Lee CC, Chen CY Biomed Res Int 18-Jun-2014
PMCID:PMC4086615
doi:10.1155/2014/761849
PMID:25045698
Ecological status and traditional knowledge of medicinal plants in Kedarnath Wildlife Sanctuary of Garhwal Himalaya, India Bhat JA, Kumar M, Bussmann RW J Ethnobiol Ethnomed 02-Jan-2013
PMCID:PMC3560114
doi:10.1186/1746-4269-9-1
PMID:23281594
Isocyasterone, an insect metamorphosing substance from Cyathula capitata H. Hikino, K. Nomoto, T. Takemoto Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97371-0
Poststerone, a metabolite of insect metamorphosing substances from Cyathula capitata. Hikino H, Nomoto K, Takemoto T Steroids 01-Oct-1970
doi:10.1016/S0039-128X(70)80122-2
PMID:5496441
Sengosterone, an insect metamorphosing substance from Cyathula capitata: structure. Hikino H, Nomoto K, Takemoto T Tetrahedron 01-Feb-1970
doi:10.1016/S0040-4020(01)97887-1
PMID:5435928

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 / Prenol lipids / Triterpenoids
(3R,4S,5R)-4-[(2R,3R)-2,3-dihydroxy-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 12305324 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
(3S,4S,5R)-4-[(2S,3R)-2,3-dihydroxy-3-[(2S,3R,5S,9S,10R,13R,14S,17S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-6-oxo-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 163067538 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5(C4(CC(C(C5)O)O)C)O)C)O)O)O 536.70 unknown https://doi.org/10.1016/S0040-4020(01)97887-1
(3S,4S,5S)-4-[(2S,3R)-2,3-dihydroxy-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 162957539 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0040-4020(01)97887-1
[(2S,3R,5R,9R,10R,13R,14S,17S)-2-acetyloxy-17-[(2R,3R)-3-acetyloxy-4-[(2R,3R,4S)-2,4-dimethyl-5-oxooxolan-3-yl]-2-hydroxybutan-2-yl]-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162964744 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)OC(=O)C)OC(=O)C)C)C)O)O)OC(=O)C 646.80 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
[(2S,3R,5R,9R,10R,13R,14S,17S)-2-acetyloxy-17-[(2R,3R)-3-acetyloxy-4-[(2S,3R,4S)-2,4-dimethyl-5-oxooxolan-3-yl]-2-hydroxybutan-2-yl]-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162964746 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)OC(=O)C)OC(=O)C)C)C)O)O)OC(=O)C 646.80 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
[(2S,3R,5S,9R,10R,13R,14S,17S)-2-acetyloxy-17-[(2R,3R)-3-acetyloxy-4-[(2R,3S,4S)-2,4-dimethyl-5-oxooxolan-3-yl]-2-hydroxybutan-2-yl]-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162964745 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)OC(=O)C)OC(=O)C)C)C)O)O)OC(=O)C 646.80 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
[2-acetyloxy-17-[3-acetyloxy-4-(2,4-dimethyl-5-oxooxolan-3-yl)-2-hydroxybutan-2-yl]-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 72827622 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)OC(=O)C)OC(=O)C)C)C)O)O)OC(=O)C 646.80 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
4-[2,3-dihydroxy-3-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl]-3,5-dimethyloxolan-2-one 554197 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
https://doi.org/10.1016/S0040-4020(01)97887-1
Cyasterone 119444 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1016/S0031-9422(00)97371-0
https://doi.org/10.1016/S0040-4020(01)97887-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
[1,3,11-trihydroxy-10-methyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-13-yl]methyl acetate 73999895 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CC(C3C2CCC4C3(C(CC(C4)O)O)C)O)COC(=O)C 490.70 unknown https://doi.org/10.1016/S0040-4020(01)97887-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
(17-acetyl-2-acetyloxy-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate 72792217 Click to see CC(=O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC(=O)C)OC(=O)C)C)C)O 446.50 unknown https://doi.org/10.1016/S0039-128X(70)80122-2
[(2S,3S,5R,9R,10R,13R,14S,17S)-17-acetyl-2-acetyloxy-14-hydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162899740 Click to see CC(=O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC(=O)C)OC(=O)C)C)C)O 446.50 unknown https://doi.org/10.1016/S0039-128X(70)80122-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2S,3R,5R,10R,13R,17S)-17-[(2R)-5-ethyl-2,3,7-trihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-5,10,13-trimethyl-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 5317804 Click to see CCC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)C)C)O)O)O)C(C)CO 522.70 unknown https://doi.org/10.1016/S0040-4020(01)97887-1
(2S,3S,5R,9R,10R,13R,14S,17S)-17-[(2S,3R,5S,6S)-5-ethyl-2,3,7-trihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 163019839 Click to see CCC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)CO 508.70 unknown https://doi.org/10.1016/S0040-4020(01)97887-1

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