General Information of the Compound
Compound ID
CP0383463
Compound Name
methyl (1S,3R,4aS,8S,8aS)-8-[(2S,3R,4S,5S,6R)-3-[[(1S,3R,4aS,8S,8aS)-5-methoxycarbonyl-1-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-methoxy-1-methyl-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate
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Structure
Formula
C35H52O21
Molecular Weight
808.78
Canonical SMILES
CO[C@H]1C[C@H]2[C@@H]([C@H](C)O1)[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1C[C@H]3[C@@H]([C@H](C)O1)[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC=C3C(=O)OC)OC=C2C(=O)OC
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InChI
InChI=1S/C35H52O21/c1-12-22-14(6-20(45-3)50-12)16(30(43)46-4)10-49-33(22)56-35-29(27(41)25(39)19(9-37)53-35)54-21-7-15-17(31(44)47-5)11-48-32(23(15)13(2)51-21)55-34-28(42)26(40)24(38)18(8-36)52-34/h10-15,18-29,32-42H,6-9H2,1-5H3/t12-,13-,14+,15+,18+,19+,20+,21+,22+,23+,24+,25+,26-,27-,28+,29+,32-,33-,34-,35-/m0/s1
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InChIKey
CLWBZMLPBZRTKE-QLUPERJSSA-N
Physicochemical Property
logP
-3.1489
Rotatable Bonds
11
Heavy Atom Count
56
Polar Areas
286.51
Hydrogen Bond Donor Count
7
Hydrogen Bond Acceptor Count
21
Complexity
56

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 145959802
ChEMBL ID
CHEMBL4164481
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01503, Signal transducer and activator of transcription 3
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000063 Hep-G2 Homo sapiens (Human)  1
1
IC50 = 21900 nM
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