ASTRAGALOSIDE II

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C43H70O15
Molecular Weight	827.0069
Optical Activity	UNSPECIFIED
Defined Stereocenters	21 / 21
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[H][C@@]1([C@@H](O)C[C@@]2(C)[C@]3([H])C[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@]5([H])[C@]6(C[C@@]36CC[C@]12C)CC[C@H](O[C@@H]7OC[C@@H](O)[C@H](O)[C@H]7OC(C)=O)C5(C)C)[C@@]8(C)CC[C@H](O8)C(C)(C)O

InChI

InChIKey=AYWNHWGQTMCQIV-PENCHUSISA-N

InChI=1S/C43H70O15/c1-20(45)54-32-28(48)22(47)18-53-36(32)57-26-10-12-43-19-42(43)14-13-39(6)33(41(8)11-9-27(58-41)38(4,5)52)21(46)16-40(39,7)25(42)15-23(34(43)37(26,2)3)55-35-31(51)30(50)29(49)24(17-44)56-35/h21-36,44,46-52H,9-19H2,1-8H3/t21-,22+,23-,24+,25-,26-,27-,28-,29+,30-,31+,32+,33-,34-,35+,36-,39+,40-,41+,42-,43+/m0/s1

HIDE SMILES / InChI

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
autophagy 17 Target ID: GO:0006914 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27261591	Inhibitor 8297
Receptor-type tyrosine-protein phosphatase C 2 Target ID: P06800 Gene ID: NA Gene Symbol: Ptprc Target Organism: Mus musculus (Mouse) Sources: https://www.ncbi.nlm.nih.gov/pubmed/23524573	Activator 1430
mTOR signaling pathway 7 Target ID: map04150 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28951595	Activator 1430

Name

Type

Language

ASTRAGALOSIDE II

Common Name

English

β-D-Glucopyranoside, (3β,6α,16β,20R,24S)-3-[(2-O-acetyl-β-D-xylopyranosyl)oxy]-20,24-epoxy-16,25-dihydroxy-9,19-cyclolanostan-6-yl-

Systematic Name

English

NSC-641295

Code

English

ASTRAGALOSIDE II (CONSTITUENT OF ASTRAGALUS) [DSC]

Code

English

ASTRASIEVERSIANIN VIII

Common Name

English

(3β,6α,16β,20R,24S)-3-[(2-O-Acetyl-β-D-xylopyranosyl)oxy]-20,24-epoxy-16,25-dihydroxy-9,19-cyclolanostan-6-yl β-D-glucopyranoside

Systematic Name

English

Code System Code Type Description

FDA UNII

0K5J34DHEN