(1'R,6R)-Benzhydrylspiro[penicillanate-6,1'-(2-benzoyl-5-methoxycarbonyl(cyclopent-4-enyl))]

ID: ALA4857287

PubChem CID: 164615822

Max Phase: Preclinical

Molecular Formula: C34H31NO6S

Molecular Weight: 581.69

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COC(=O)C1=CCC(C(=O)c2ccccc2)C12C(=O)N1[C@@H](C(=O)OC(c3ccccc3)c3ccccc3)C(C)(C)S[C@@H]12

Standard InChI:  InChI=1S/C34H31NO6S/c1-33(2)28(30(38)41-27(22-15-9-5-10-16-22)23-17-11-6-12-18-23)35-31(39)34(32(35)42-33)24(19-20-25(34)29(37)40-3)26(36)21-13-7-4-8-14-21/h4-18,20,24,27-28,32H,19H2,1-3H3/t24?,28-,32+,34?/m0/s1

Standard InChI Key:  APZMYFSANJQMNC-XIHPHXFXSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4857287

    ---

Associated Targets(Human)

TZM (838 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 581.69Molecular Weight (Monoisotopic): 581.1872AlogP: 5.37#Rotatable Bonds: 7
Polar Surface Area: 89.98Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 5.86CX LogD: 5.86
Aromatic Rings: 3Heavy Atoms: 42QED Weighted: 0.21Np Likeness Score: 0.42

References

1. Alves NG, Bártolo I, Alves AJS, Fontinha D, Francisco D, Lopes SMM, Soares MIL, Simões CJV, Prudêncio M, Taveira N, Pinho E Melo TMVD..  (2021)  Synthesis and structure-activity relationships of new chiral spiro-β-lactams highly active against HIV-1 and Plasmodium.,  219  [PMID:33887681] [10.1016/j.ejmech.2021.113439]

Source