CHEBI:142487 - (20S)-ginsenoside Rh1

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ChEBI Name (20S)-ginsenoside Rh1
ChEBI ID CHEBI:142487
ChEBI ASCII Name (20S)-ginsenoside Rh1
Definition A tetracyclic triterpenoid that is (20S)-protopanaxadiol which is substituted by β-D-glucoside at the 6α position.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Kristian Axelsen
Supplier Information
Download Molfile XML SDF
Formula C36H62O9
Net Charge 0
Average Mass 638.873
Monoisotopic Mass 638.43938
InChI InChI=1S/C36H62O9/c1-19(2)10-9-13-36(8,43)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(39)32(3,4)30(33)22(17-35(24,34)7)44-31-29(42)28(41)27(40)23(18-37)45-31/h10,20-31,37-43H,9,11-18H2,1-8H3/t20-,21+,22-,23+,24+,25-,26-,27+,28-,29+,30-,31+,33+,34+,35+,36-/m0/s1
InChIKey RAQNTCRNSXYLAH-RFCGZQMISA-N
SMILES [C@]12([C@]3([C@]([H])([C@@H](C[C@]2([H])[C@@]4([C@@]([H])([C@H](C1)O[C@@H]5O[C@@H]([C@H]([C@@H]([C@H]5O)O)O)CO)C([C@H](CC4)O)(C)C)C)O)[C@]([H])(CC3)[C@](CCC=C(C)C)(O)C)C)C
Metabolite of Species Details
Panax vietnamensis (NCBI:txid106132) See: PubMed
Panax ginseng (NCBI:txid4054) See: PubMed
Panax ginseng (NCBI:txid4054) Found in leaf (BTO:0000713). See: PubMed
Panax notoginseng (NCBI:txid44586) Found in root (BTO:0001188). See: Zhou, J., Wu, M.Z., Taniyasu, S., Besso, H., Tanaka, O., Saruwatari, Y. and Fuwa, T. (1981) Dammarane-saponins of sanchi-ginseng, roots of Panax notoginseng (BURK.) F.H. CHEN (Araliaceae): Structures of new saponins, notoginsenosides-R1 and -R2, and identification of ginsenosides-Rg2 and -Rh1. Chem. Pharm. Bull., 29(10), 2844-2850.
Panax notoginseng (NCBI:txid44586) Found in root (BTO:0001188). See: Qiu, L., Jiao, Y., Huang, G.K., Xie, J.Z., Miao, J.H. and Yao, X.S. (2014) New dammarane-type saponins from the roots of Panax notoginseng. Helvetica Chemica Acta, 97(1), 102-111.
Panax notoginseng (NCBI:txid44586) Found in root (BTO:0001188). See: PubMed
Panax quinquefolius (NCBI:txid44588) Found in root (BTO:0001188). See: PubMed
Panax japonicus (NCBI:txid44685) Found in rhizome (BTO:0001181). See: PubMed
Gynostemma yixingense (NCBI:txid555433) See: PubMed
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via saponin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (20S)-ginsenoside Rh1 (CHEBI:142487) has parent hydride dammarane (CHEBI:36488)
(20S)-ginsenoside Rh1 (CHEBI:142487) has role plant metabolite (CHEBI:76924)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a β-D-glucoside (CHEBI:22798)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a 12β-hydroxy steroid (CHEBI:36847)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a 3β-hydroxy steroid (CHEBI:36836)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a 3β-hydroxy-4,4-dimethylsteroid (CHEBI:143563)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a ginsenoside (CHEBI:74978)
(20S)-ginsenoside Rh1 (CHEBI:142487) is a tetracyclic triterpenoid (CHEBI:26893)
IUPAC Name
(3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl β-D-glucopyranoside
Synonyms Sources
(20S)-ginsenoside Rh1 UniProt
(20S)-ginsenoside Rh1 ChEBI
Manual Xrefs Databases
C00030402 KNApSAcK
CPD-15446 MetaCyc
FDB019175 FooDB
HMDB0039554 HMDB
View more database links
Registry Numbers Types Sources
5786038 Reaxys Registry Number Reaxys
63223-86-9 CAS Registry Number ChemIDplus
63223-86-9 CAS Registry Number KNApSAcK
Citations Waiting for Citations Types Sources
11210151 PubMed citation Europe PMC
11325227 PubMed citation Europe PMC
16651785 PubMed citation Europe PMC
19781603 PubMed citation Europe PMC
20686271 PubMed citation Europe PMC
23291557 PubMed citation Europe PMC
26032089 PubMed citation SUBMITTER
26200131 PubMed citation Europe PMC
29329463 PubMed citation Europe PMC
Last Modified
05 November 2019