(1S,2R,4aS,5R,8aR)-1-((E)-2-((S)-4-(tert-butyldimethylsilyloxy)-2-oxodihydrofuran-3(2H)-ylidene)ethyl)-5-(hydroxymethyl)-5,8a-dimethylhexahydro-1H-spiro[naphthalene-2,2'-oxiran]-6(7H)-one

ID: ALA4173895

Chembl Id: CHEMBL4173895

PubChem CID: 145951232

Max Phase: Preclinical

Molecular Formula: C26H42O6Si

Molecular Weight: 478.70

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)(C)[Si](C)(C)O[C@@H]1COC(=O)/C1=C/C[C@@H]1[C@]2(CC[C@H]3[C@@]1(C)CCC(=O)[C@@]3(C)CO)CO2

Standard InChI:  InChI=1S/C26H42O6Si/c1-23(2,3)33(6,7)32-18-14-30-22(29)17(18)8-9-20-24(4)12-11-21(28)25(5,15-27)19(24)10-13-26(20)16-31-26/h8,18-20,27H,9-16H2,1-7H3/b17-8+/t18-,19+,20+,24-,25+,26+/m1/s1

Standard InChI Key:  BWSROLQPRWNMCH-SFQQMKOASA-N

Alternative Forms

  1. Parent:

    ALA4173895

    ---

Associated Targets(Human)

STAT3 Tchem Signal transducer and activator of transcription 3 (3313 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AD293 (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
STAT1 Tchem Signal transducer and activator of transcription 1-alpha/beta (808 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 478.70Molecular Weight (Monoisotopic): 478.2751AlogP: #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