Cas no 174721-08-5 (Ginsenoside Rh4)

Ginsenoside Rh4 is a rare protopanaxadiol-type saponin primarily isolated from Panax ginseng and related species. It exhibits notable pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. Structurally characterized by a dammarane-type triterpenoid skeleton with sugar moieties, Rh4 demonstrates enhanced bioavailability compared to higher-molecular-weight ginsenosides due to its smaller glycosylation pattern. Research highlights its ability to modulate cellular signaling pathways such as NF-κB and MAPK, contributing to its chemopreventive potential. Additionally, Ginsenoside Rh4 shows neuroprotective effects by attenuating oxidative stress and mitochondrial dysfunction. Its low cytotoxicity and targeted action on tumor cells make it a promising candidate for adjuvant therapy in oncology and age-related diseases.
Ginsenoside Rh4 structure
Ginsenoside Rh4 structure
Product Name:Ginsenoside Rh4
CAS No:174721-08-5
MF:C36H60O8
MW:620.856812477112
CID:823221
PubChem ID:21599928
Update Time:2025-07-02

Ginsenoside Rh4 Chemical and Physical Properties

Names and Identifiers

    • Ginsenoside RH4
    • Ginsenoside Rh(4)
    • beta-D-glucopyranoside, (3beta,6alpha,12beta,20E)-3,12-dihydroxydammara-20(22),24-dien-6-yl
    • (3beta,6alpha,12beta,20E)-3,12-Dihydroxydammara-20(22),24-dien-6-yl-beta-D-glucopyranoside
    • (2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-Dihydroxy-4,4,8,10,14-pentamethyl-17-
    • CHEBI:176255
    • (2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-4,4,8,10,14-pentamethyl-17-[(2E)-6-methylhepta-2,5-dien-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
    • DTXSID001317113
    • CHEMBL504029
    • AKOS030526659
    • AC-34672
    • 174721-08-5
    • FS-7833
    • HY-N0905
    • NCGC00485965-01
    • MFCD22125012
    • CS-3843
    • (+)-Ginsenoside Rh4
    • (2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-4,4,8,10,14-pentamethyl-17-((2E)-6-methylhepta-2,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta(a)phenanthren-6-yl)oxy)-6-(hydroxymethyl)oxane-3,4,5-triol
    • DA-63767
    • (3beta,6alpha,12beta,20E)-3,12-Dihydroxydammara-20(22),24-dien-6-yl beta-D-glucopyranoside;
    • 6-O-glucopyranosyldammar-20(22),24-diene-3,6,12-triol
    • Ginsenoside Rh4
    • MDL: MFCD22125012
    • Inchi: 1S/C36H60O8/c1-19(2)10-9-11-20(3)21-12-15-35(7)27(21)22(38)16-25-34(6)14-13-26(39)33(4,5)31(34)23(17-36(25,35)8)43-32-30(42)29(41)28(40)24(18-37)44-32/h10-11,21-32,37-42H,9,12-18H2,1-8H3/b20-11+/t21-,22-,23+,24-,25-,26+,27+,28-,29+,30-,31+,32-,34-,35-,36-/m1/s1
    • InChI Key: OZTXYFOXQFKYRP-TXRYYSRHSA-N
    • SMILES: O([C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)[C@H]1C[C@@]2(C)[C@]3(C)CC[C@H](/C(=C/C/C=C(\C)/C)/C)[C@H]3[C@@H](C[C@@H]2[C@@]2(C)CC[C@@H](C(C)(C)[C@@H]21)O)O

Computed Properties

  • Exact Mass: 620.42900
  • Monoisotopic Mass: 620.42881887 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 6
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 44
  • Rotatable Bond Count: 6
  • Complexity: 1120
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 15
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 140
  • Molecular Weight: 620.9
  • XLogP3: 5.6

Experimental Properties

  • Color/Form: Powder
  • Density: 1.21
  • Melting Point: No data available
  • Boiling Point: 723.4±60.0 °C at 760 mmHg
  • Flash Point: 391.3±32.9 °C
  • Refractive Index: 1.579
  • PSA: 139.84000
  • LogP: 4.10080

Ginsenoside Rh4 Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Ginsenoside Rh4 Production Method

Production Method 1

Reaction Conditions
1.1 Solvents: Ethanol ,  Water ;  4 d, 26 °C
Reference
Microbial Transformation of 20(S)-Protopanaxatriol-Type Saponins by Absidia coerulea
Chen, Guangtong; Yang, Min; Lu, Zhiqiang; Zhang, Jinqiang; Huang, Huilian; et al, Journal of Natural Products, 2007, 70(7), 1203-1206

Production Method 2

Reaction Conditions
1.1 Solvents: Ethanol ,  Water ;  4 d, 26 °C
Reference
Microbial Transformation of 20(S)-Protopanaxatriol-Type Saponins by Absidia coerulea
Chen, Guangtong; et al, Journal of Natural Products, 2007, 70(7), 1203-1206

Production Method 3

Reaction Conditions
1.1 Solvents: Ethanol ,  Water ;  4 d, 26 °C
Reference
Microbial Transformation of 20(S)-Protopanaxatriol-Type Saponins by Absidia coerulea
Chen, Guangtong; et al, Journal of Natural Products, 2007, 70(7), 1203-1206

Ginsenoside Rh4 Raw materials

Ginsenoside Rh4 Preparation Products

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