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CAS 98891-44-2

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Pseudolaric acid A O-β-D-glucopyranoside

Description:
Pseudolaric acid A O-β-D-glucopyranoside is a glycoside derived from pseudolaric acid A, which is a natural compound found in the bark of the Pseudolarix amabilis tree. This substance is characterized by its structural composition, which includes a pseudolaric acid moiety linked to a β-D-glucopyranoside unit. It exhibits various biological activities, including potential anti-inflammatory and anti-tumor properties, making it of interest in pharmacological research. The compound is typically studied for its effects on cellular processes and its potential therapeutic applications. In terms of solubility, glycosides like this one are often more soluble in water compared to their aglycone counterparts due to the presence of the hydrophilic sugar moiety. The compound's molecular interactions and stability can be influenced by factors such as pH and temperature. Overall, Pseudolaric acid A O-β-D-glucopyranoside represents a fascinating area of study within natural product chemistry and pharmacognosy.
Formula:C28H38O11
InChI:InChI=1S/C28H38O11/c1-15-7-11-27-12-9-19(28(27,13-8-15)38-17(3)30)26(4,39-25(27)35)10-5-6-16(2)23(34)37-24-22(33)21(32)20(31)18(14-29)36-24/h5-7,10,18-22,24,29,31-33H,8-9,11-14H2,1-4H3/b10-5+,16-6+/t18-,19+,20-,21+,22-,24+,26-,27-,28+/m1/s1
InChI key:InChIKey=IVYWRYGMQNKDQB-VHJBJYHKSA-N
SMILES:O(C(C)=O)[C@]12[C@@]3(CC[C@]1([C@](/C=C/C=C(/C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=O)\C)(C)OC3=O)[H])CC=C(C)CC2
Synonyms:
  • 1H-4,9a-Ethanocyclohepta[c]pyran, 2,4-pentadienoic acid deriv.
  • Pseudolaric acid A O-β-D-glucopyranoside
  • Pseudolaric acid A β-D-glucoside
  • β-D-Glucopyranose, 1-[(2E,4E)-5-[(3R,4S,4aS,9aR)-4a-(acetyloxy)-3,4,4a,5,6,9-hexahydro-3,7-dimethyl-1-oxo-1H-4,9a-ethanocyclohepta[c]pyran-3-yl]-2-methyl-2,4-pentadienoate]
  • Pseudolaric acid A-glucopyranoside
  • Pseudolaricid A-O-β-D-glucopyranoside
  • PubChem ID: 44566375
  • Pseudolaric acid A beta-D-glucoside
  • Pseudolaric Acid A-O-beta-D-glucopyranoside
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