BETA-D-GLUCOPYRANOSE, 1,3,6-TRIS(3,4,5-TRIHYDROXYBENZOATE)

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C27H24O18
Molecular Weight	636.4687
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BETA-D-GLUCOPYRANOSE, 1,3,6-TRIS(3,4,5-TRIHYDROXYBENZOATE)

Structure Search

SMILES

O[C@@H]1[C@@H](COC(=O)C2=CC(O)=C(O)C(O)=C2)O[C@@H](OC(=O)C3=CC(O)=C(O)C(O)=C3)[C@H](O)[C@H]1OC(=O)C4=CC(O)=C(O)C(O)=C4

InChI

InChIKey=RNKMOGIPOMVCHO-SJMVAQJGSA-N

InChI=1S/C27H24O18/c28-11-1-8(2-12(29)18(11)34)24(39)42-7-17-21(37)23(44-25(40)9-3-13(30)19(35)14(31)4-9)22(38)27(43-17)45-26(41)10-5-15(32)20(36)16(33)6-10/h1-6,17,21-23,27-38H,7H2/t17-,21-,22-,23+,27+/m1/s1

HIDE SMILES / InChI

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21959301 | https://www.ncbi.nlm.nih.gov/pubmed/19881284

1,3,6-tri-O-galloyl-β-D-glucose was isolated from Euphorbia lunulata Bge and from the leaves of Sapium insigne (ROYLE) BENTH. ex HOOK. fil. It was shown, that this compound inhibited the following processes: differentiation of 3T3-L1 preadipocytes and triglyceride accumulation in mature adipocytes, and nitric oxide production in RAW 264.7 cells.

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
cell differentiation 3 Target ID: GO:0030154 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21959301	Inhibitor 8297

PubMed

Title	Date	PubMed
Inhibitory effects of constituents from Euphorbia lunulata on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.	2011 Sep 29	21959301

Name

Type

Language

BETA-D-GLUCOPYRANOSE, 1,3,6-TRIS(3,4,5-TRIHYDROXYBENZOATE)

Common Name

English

1,3,6-TRI-O-GALLOYLGLUCOSE

Common Name

English

1,3,6-TRI-O-GALLOYL-.BETA.-D-GLUCOPYRANOSE

Common Name

English

.BETA.-D-GLUCOPYRANOSE, 1,3,6-TRIS(3,4,5-TRIHYDROXYBENZOATE)

Systematic Name

English

NSC-69861

Code

English

J303.464J

Code

English

Code System Code Type Description

CAS

18483-17-5