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Details Top

Internal ID UUID644042264f778559920606
Scientific name Corethrodendron multijugum
Authority (Maxim.) B.H.Choi & H.Ohashi
First published in Taxon52: 573 (2003)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hedysarum multijugum Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg, sér. 3, 27: 464 (1882)
Hedysarum multijugum var. inermis Liu
Corethrodendron multijugum f. albiflorum (Y.H.Wu) X.Y.Zhu Biodivers. Sci.23: 248 (2015)
Hedysarum multijugum f. albiflorus Y.H.Wu Bull. Bot. Res., Harbin24: 4 (2004)
Hedysarum multijugum var. apiculatum Sprague Bot. Mag.132: t. 8091 (1906)

Common names Top

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Language Common/alternative name
Chinese 红花岩黄耆
Chinese 红花岩黄芪
Chinese 红花山竹子
Chinese 红花羊柴

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-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Qinghai
      • Tibet

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001034249
Tropicos 100316178
KEW urn:lsid:ipni.org:names:70029966-1
The Plant List tro-100316178
Open Tree Of Life 3922414
NCBI Taxonomy 1402425
IPNI 70029966-1
GBIF 3973632
USDA GRIN 434046
CMAUP NPO4095

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
Geographical patterns and environmental influencing factors of variations in Asterothamnus centraliasiaticus seed traits on Qinghai-Tibetan plateau Li Z, Ma Y, Liu Y, Wang Y, Wang X Front Plant Sci 28-Mar-2024
PMCID:PMC11006976
doi:10.3389/fpls.2024.1366512
PMID:38606068
Application of artificial intelligence (AI) to control COVID-19 pandemic: Current status and future prospects Ashique S, Mishra N, Mohanto S, Garg A, Taghizadeh-Hesary F, Gowda BH, Chellappan DK Heliyon 09-Feb-2024
PMCID:PMC10869876
doi:10.1016/j.heliyon.2024.e25754
PMID:38370192
Hu-Zhang Qing-Mai Formulation anti-oxidative stress alleviates diabetic retinopathy: Network pharmacology analysis and in vitro experiment Wu X, Mu L, Dong Z, Wu J, Zhang S, Su J, Zhang Y Medicine (Baltimore) 08-Sep-2023
PMCID:PMC10489428
doi:10.1097/MD.0000000000035034
PMID:37682156
Network pharmacology prediction and molecular docking-based strategy to discover the potential pharmacological mechanism of Huang–Qi–Gui–Zhi–Wu–Wu decoction against deep vein thrombosis Fan W, Lan S, Yang Y, Liang J J Orthop Surg Res 30-Jun-2023
PMCID:PMC10314554
doi:10.1186/s13018-023-03948-6
PMID:37391801
Anti-inflammatory and antioxidant traditional Chinese Medicine in treatment and prevention of osteoporosis Li Q, Tian C, Liu X, Li D, Liu H Front Pharmacol 27-Jun-2023
PMCID:PMC10335577
doi:10.3389/fphar.2023.1203767
PMID:37441527
The complete chloroplast genome of Corethrodendron multijugum (Fabaceae: Corethrodendron) and phylogenetic analysis Zhang LJ, Liu Y, Shi JJ Mitochondrial DNA B Resour 01-Jun-2023
PMCID:PMC10236963
doi:10.1080/23802359.2023.2209387
PMID:37275398
New insights for infection mechanism and potential targets of COVID-19: Three Chinese patent medicines and three Chinese medicine formulas as promising therapeutic approaches Jia K, Li Y, Liu T, Gu X, Li X Chin Herb Med 08-Mar-2023
PMCID:PMC9993661
doi:10.1016/j.chmed.2022.06.014
PMID:37220535
Mechanism of Xiezhuo Huayu Yiqi Tongluo Formula in the Treatment of Uric Acid Nephropathy Based on Network Pharmacology, Molecular Docking, and In Vivo Experiments Fan L, Guo Y, Wu Q, Hu T, Chen X, Guo J, Liu Y, Lu Y, Lin M Evid Based Complement Alternat Med 21-Feb-2023
PMCID:PMC9974263
doi:10.1155/2023/6931644
PMID:36865745
Tiao-Bu-Fei-Shen Formula Improves Glucocorticoid Resistance of Chronic Obstructive Pulmonary Disease via Downregulating the PI3K-Akt Signaling Pathway and Promoting GRα Expression Zhou P, Ma J, Yu W, Chen K, Zhang W, Zhou J Evid Based Complement Alternat Med 11-Feb-2023
PMCID:PMC9938767
doi:10.1155/2023/4359616
PMID:36820399
Deciphering the protective effect of Buzhong Yiqi Decoction on osteoporotic fracture through network pharmacology and experimental validation Hua Z, Dai S, Li S, Wang J, Peng H, Rong Y, Yu H, Liu M J Orthop Surg Res 04-Feb-2023
PMCID:PMC9898002
doi:10.1186/s13018-023-03545-7
PMID:36737821
Inflammatory response: The target for treating hyperpigmentation during the repair of a burn wound Zhong C, Liang G, Li P, Shi K, Li F, Zhou J, Xu D Front Immunol 01-Feb-2023
PMCID:PMC9929571
doi:10.3389/fimmu.2023.1009137
PMID:36817442
Traditional Chinese medicine for transformation of gastric precancerous lesions to gastric cancer: A critical review Zhong YL, Wang PQ, Hao DL, Sui F, Zhang FB, Li B World J Gastrointest Oncol 15-Jan-2023
PMCID:PMC9850768
doi:10.4251/wjgo.v15.i1.36
PMID:36684050
Exploration of the mechanism by which Huangqi Guizhi Wuwu decoction inhibits Lps-induced inflammation by regulating macrophage polarization based on network pharmacology Wang S, Ji T, Wang L, Qu Y, Wang X, Wang W, Lv M, Wang Y, Li X, Jiang P BMC Complement Med Ther 09-Jan-2023
PMCID:PMC9830836
doi:10.1186/s12906-022-03826-4
PMID:36624435
Identification of Markers for Diagnosis and Treatment of Diabetic Kidney Disease Based on the Ferroptosis and Immune Ma J, Li C, Liu T, Zhang L, Wen X, Liu X, Fan W Oxid Med Cell Longev 23-Nov-2022
PMCID:PMC9712001
doi:10.1155/2022/9957172
PMID:36466094
Hedysarum multijugum Maxim treats ulcerative colitis through the PI3K-AKT and TNF signaling pathway according to network pharmacology and molecular docking Zhang Z, Chong W, Xie X, Liu Y, Shang L, Li L Ann Transl Med 01-Oct-2022
PMCID:PMC9652569
doi:10.21037/atm-22-4815
PMID:36388782

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tetracosanol 10472 Click to see CCCCCCCCCCCCCCCCCCCCCCCCO 354.70 unknown via CMAUP database
Docosanol 12620 Click to see CCCCCCCCCCCCCCCCCCCCCCO 326.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown via CMAUP database
1-Eicosanol 12404 Click to see CCCCCCCCCCCCCCCCCCCCO 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Bauerenol 111220 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Eburicol 9803310 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
Lanosta-7,24-dienol 12302189 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Lanosterol 246983 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
31-Norlanostenol 14845298 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C 414.70 unknown via CMAUP database
4alpha,14alpha-Dimethyl-5alpha-cholesta-8,24-dien-3beta-ol 15101557 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC=C(C)C)C)C 412.70 unknown via CMAUP database
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
Lophenol 160482 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
31-Norcycloartenol 14524546 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC=C(C)C)C 412.70 unknown via CMAUP database
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholesta-5,24-dien-3beta-ol 5283643 Click to see CCC(=C(C)C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown via CMAUP database
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,4-(4-Methoxy-6-hydroxy-1,2-phenyleneoxy)-5-hydroxy-7-methoxy-2H-1-benzopyran 5316760 Click to see COC1=CC(=C2C(=C1)OCC3=C2OC4=CC(=CC(=C34)O)OC)O 314.29 unknown via CMAUP database

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