((1S,2S,4aS,5R,8aR)-1-((E)-2-((R)-4-(tert-butyldimethylsilyloxy)-2-oxodihydrofuran-3(2H)-ylidene)ethyl)-5,8a-dimethyl-6-oxooctahydro-1H-spiro[naphthalene-2,2'-oxirane]-5-yl)methyl acetate

ID: ALA4171438

Chembl Id: CHEMBL4171438

PubChem CID: 145950270

Max Phase: Preclinical

Molecular Formula: C28H44O7Si

Molecular Weight: 520.74

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CC(=O)OC[C@]1(C)C(=O)CC[C@@]2(C)[C@H](C/C=C3/C(=O)OC[C@@H]3O[Si](C)(C)C(C)(C)C)[C@@]3(CC[C@@H]21)CO3

Standard InChI:  InChI=1S/C28H44O7Si/c1-18(29)33-16-27(6)21-11-14-28(17-34-28)22(26(21,5)13-12-23(27)30)10-9-19-20(15-32-24(19)31)35-36(7,8)25(2,3)4/h9,20-22H,10-17H2,1-8H3/b19-9+/t20-,21-,22-,26+,27-,28+/m0/s1

Standard InChI Key:  KHPKUNRFOODLLZ-DIBUFECGSA-N

Alternative Forms

1. Parent:

   

   ALA4171438

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 520.74

Molecular Weight (Monoisotopic): 520.2856

AlogP: ┄

#Rotatable Bonds: ┄

Polar Surface Area: ┄

Molecular Species: ┄

HBA: ┄

HBD: ┄

#RO5 Violations: ┄

HBA (Lipinski): ┄

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: ┄

CX LogD: ┄

Aromatic Rings: ┄

Heavy Atoms: ┄

QED Weighted: ┄

Np Likeness Score: ┄

References

1. Chen SR, Li F, Ding MY, Wang D, Zhao Q, Wang Y, Zhou GC, Wang Y..  (2018)  Andrographolide derivative as STAT3 inhibitor that protects acute liver damage in mice.,  26  (18): [PMID:30228000] [10.1016/j.bmc.2018.09.002]

Source

Source(1):

• Scientific Literature