Sophoricoside - ≥98% , CAS No.152-95-4

CAS: 152-95-4 Cat. No.: S292468 Formule: C₂₁H₂₀O₁₀ Poids moléculaire: 432.38 PubChem CID: 5321398

GRADE & PURITY ≥98%

Synonyms

UNII-J0407L5MGM | AI3-52559 | AS-12103 | HY-N0423 | (2S)-N-Boc-5-methylpyrrolidine-2-carboxylicacid | Sophoricoside | 5,7-dihydroxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one | Q-100181 | GENISTEIN, 4'-.BETA

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

The blood sugar of the rabbits was increased temporarily by the injection of Huaijiao. According to Nanjing Pharmaceutical Research Institute, genistein and kaempferol from Sophora japonica have the effects of interfering with the transport of pregnant eggs, terminating the implantation of pregnant eggs and resisting early pregnancy, which may be related to the activity of estrogen. Taking genistein and Sophora japonica for a long time in a small amount has a significant anti fertility effect on female mice without affecting the mating rate and growth.

The toxic effect of soaking lambs with Sophora horn can reduce the red blood cells of rabbits and guinea pigs, especially the effect of pods. Sophora seed extract can make rabbit, pig and human red blood cells agglutinate. Seeds, pods and pulp all contain anti-A, anti-B and anti-H lectins. Sophora japonica contains phytohemagglutinin drugs and can promote lymphocyte transformation

Specifications

Synonymes

UNII-J0407L5MGM | AI3-52559 | AS-12103 | HY-N0423 | (2S)-N-Boc-5-methylpyrrolidine-2-carboxylicacid | Sophoricoside | 5,7-dihydroxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one | Q-100181 | GENISTEIN, 4'-.BETA

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

• Pubchem Sid: 488195343
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488195343
• Sourires canoniques: C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O
• IUPAC Name: 5,7-dihydroxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
• InChIKey: ISQRJFLLIDGZEP-CMWLGVBASA-N
• INCHI: 1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-3-1-9(2-4-11)12-8-29-14-6-10(23)5-13(24)16(14)17(12)25/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1
• Isomères SMILES: C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
• PubChem CID: 5321398
• Poids moléculaire: 432.38

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Classe Isoflavonoids
      • Subclass Isoflavonoid O-glycosides

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: Isoflavonoids
• Subclass: Isoflavonoid O-glycosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Isoflavonoid O-glycosides
• Alternative Parents: Hydroxyisoflavonoids Isoflavones Fatty acyl glycosides of mono- and disaccharides Phenolic glycosides Alkyl glycosides Hexoses Chromones O-glycosyl compounds Phenoxy compounds Phenol ethers Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes Heteroaromatic compounds Vinylogous acids Secondary alcohols Polyols Oxacyclic compounds Acetals Organic oxides Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Isoflavonoid-4p-o-glycoside - Isoflavonoid o-glycoside - Isoflavone - Hydroxyisoflavonoid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - Hexose monosaccharide - Alkyl glycoside - Chromone - Glycosyl compound - O-glycosyl compound - 1-benzopyran - Benzopyran - Phenol ether - Phenoxy compound - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Monosaccharide - Pyran - Oxane - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Primary alcohol - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.
• 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

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NA Neuraminidase (1107 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Rotation spécifique [α]: -18 ° (C=1, Pyridine)
• Point de fusion (°C): 297°C
• Poids moléculaire: 432.400 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 4
• Exact Mass: 432.106 Da
• Monoisotopic Mass: 432.106 Da
• Topological Polar Surface Area: 166.000 Ų
• Heavy Atom Count: 31
• Formal Charge: 0
• Complexity: 675.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• 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