Ethyl (1S,4S,5R,7S)-7-acetoxy-4-isopropyl-8-oxospiro[4.5]decane-1-carboxylate

ID: ALA3765212

Chembl Id: CHEMBL3765212

PubChem CID: 127039204

Max Phase: Preclinical

Molecular Formula: C18H28O5

Molecular Weight: 324.42

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOC(=O)[C@H]1CC[C@@H](C(C)C)[C@]12CCC(=O)[C@@H](OC(C)=O)C2

Standard InChI:  InChI=1S/C18H28O5/c1-5-22-17(21)14-7-6-13(11(2)3)18(14)9-8-15(20)16(10-18)23-12(4)19/h11,13-14,16H,5-10H2,1-4H3/t13-,14+,16-,18+/m0/s1

Standard InChI Key:  PXJZJQSTXFCVEX-JSSFPYSZSA-N

Alternative Forms

  1. Parent:

    ALA3765212

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Associated Targets(Human)

HSD11B1 Tclin 11-beta-hydroxysteroid dehydrogenase 1 (5910 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD11B2 Tchem 11-beta-hydroxysteroid dehydrogenase 2 (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BJ (6930 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: 324.42Molecular Weight (Monoisotopic): 324.1937AlogP: 2.90#Rotatable Bonds: 4
Polar Surface Area: 69.67Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.81CX LogD: 2.81
Aromatic Rings: Heavy Atoms: 23QED Weighted: 0.74Np Likeness Score: 1.76

References

1. Ling T, Gautam LN, Griffith E, Das S, Lang W, Shadrick WR, Shelat A, Lee R, Rivas F..  (2016)  Synthesis and evaluation of colletoic acid core derivatives.,  110  [PMID:26820555] [10.1016/j.ejmech.2016.01.027]

Source