Cimiracemoside C - ≥99% , CAS No.256925-92-5

CAS: 256925-92-5 Cat. No.: C647384 Molecular Weight: 620.81 PubChem CID: 15541911

GRADE & PURITY ≥99%

Synonyms

AKOS032948479 | alpha-L-Arabinopyranoside, (3beta,15alpha,16alpha,23R,24S)-16,23:16,24-diepoxy-15,25-dihydroxy-9,19-cyclolanostan-3-yl | UNII-4DC28J6R1K | SCHEMBL4921749 | Q27259441 | (2S,3R,4S,5S)-2-[[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hyd

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview

Cimiracemoside C is an active component of Cimicifuga racemosa , activates AMPK , has the potential activity against diabetes.

Form:Solid

Specifications

Synonyms

AKOS032948479 | alpha-L-Arabinopyranoside, (3beta, 15alpha, 16alpha, 23R, 24S)-16, 23:16, 24-diepoxy-15, 25-dihydroxy-9, 19-cyclolanostan-3-yl | UNII-4DC28J6R1K | SCHEMBL4921749 | Q27259441 | (2S, 3R, 4S, 5S)-2-[[(1S, 2R, 3S, 4R, 7R, 9S, 12R, 14S, 17R, 18R, 19R, 21R, 22S)-2-hyd

Specifications & Purity

≥99%

Biochemical and Physiological Mechanisms

Cimiracemoside C is an active component of Cimicifuga racemosa , activates AMPK , has the potential activity against diabetes.

Storage

Protected from light, Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

ACTIVATOR

Purity

≥99%

Names and Identifiers

• Canonical Smiles: CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)O
• IUPAC Name: (2S,3R,4S,5S)-2-[[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol
• InChIKey: BTPYUWOBZFGKAI-BKJHYQRZSA-N
• INCHI: 1S/C35H56O9/c1-17-14-19-26(30(4,5)40)44-35(43-19)25(17)31(6)12-13-34-16-33(34)11-10-22(42-27-24(38)23(37)18(36)15-41-27)29(2,3)20(33)8-9-21(34)32(31,7)28(35)39/h17-28,36-40H,8-16H2,1-7H3/t17-,18+,19-,20+,21+,22+,23+,24-,25-,26+,27+,28-,31-,32-,33-,34+,35+/m1/s1
• Isomeric SMILES: C[C@@H]1C[C@@H]2[C@H](O[C@]3([C@H]1[C@]4(CC[C@@]56C[C@@]57CC[C@@H](C([C@@H]7CC[C@H]6[C@@]4([C@H]3O)C)(C)C)O[C@H]8[C@@H]([C@H]([C@H](CO8)O)O)O)C)O2)C(C)(C)O
• Alternate CAS: 256925-92-5
• PubChem CID: 15541911
• MeSH Entry Terms: cimigenol 3-O-alpha-L-arabinopyranoside;cimigenol 3AAP
• Molecular Weight: 620.81

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Steroids and steroid derivatives
      • Subclass Steroidal glycosides
        • Level5 Steroidal saponins
          • Level6 Cucurbitacin glycosides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Steroids and steroid derivatives
• Subclass: Steroidal glycosides
• Intermediate Tree Nodes: Steroidal saponins
• Direct Parent: Cucurbitacin glycosides
• Alternative Parents: Triterpenoids Cycloartanols and derivatives Hydroxysteroids O-glycosyl compounds Oxepanes Ketals Oxanes Monosaccharides Tertiary alcohols 1,3-dioxolanes Secondary alcohols Cyclic alcohols and derivatives Polyols Oxacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Cucurbitacin glycoside skeleton - Cycloartanol-skeleton - 9b,19-cyclo-lanostane-skeleton - Cycloartane-skeleton - Triterpenoid - 15-hydroxysteroid - Hydroxysteroid - Glycosyl compound - O-glycosyl compound - Oxepane - Ketal - Oxane - Monosaccharide - Cyclic alcohol - Tertiary alcohol - Meta-dioxolane - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Organooxygen compound - Alcohol - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: H2O : <0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) DMSO : <1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble or slightly soluble)
• Molecular Weight: 620.800 g/mol
• XLogP3: 3.700
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 3
• Exact Mass: 620.392 Da
• Monoisotopic Mass: 620.392 Da
• Topological Polar Surface Area: 138.000 Ų
• Heavy Atom Count: 44
• Formal Charge: 0
• Complexity: 1210.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 17
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1