Bis(4-octylthiocarbonothioyl-1-piperazinylthiocarbonyl)disulfide

ID: ALA3794397

Chembl Id: CHEMBL3794397

PubChem CID: 127029464

Max Phase: Preclinical

Molecular Formula: C28H50N4S8

Molecular Weight: 699.27

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCCCSC(=S)N1CCN(C(=S)SSC(=S)N2CCN(C(=S)SCCCCCCCC)CC2)CC1

Standard InChI:  InChI=1S/C28H50N4S8/c1-3-5-7-9-11-13-23-37-25(33)29-15-19-31(20-16-29)27(35)39-40-28(36)32-21-17-30(18-22-32)26(34)38-24-14-12-10-8-6-4-2/h3-24H2,1-2H3

Standard InChI Key:  RYAQIHDLIWLDCA-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3794397

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Associated Targets(non-human)

Trichomonas vaginalis (2376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sporothrix schenckii (1580 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton mentagrophytes (4846 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida parapsilosis (8521 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: 699.27Molecular Weight (Monoisotopic): 698.1801AlogP: 8.93#Rotatable Bonds: 14
Polar Surface Area: 12.96Molecular Species: HBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 11.40CX LogD: 11.40
Aromatic Rings: 0Heavy Atoms: 40QED Weighted: 0.10Np Likeness Score: -0.29

References

1. Lal N, Jangir S, Bala V, Mandalapu D, Sarswat A, Kumar L, Jain A, Kumar L, Kushwaha B, Pandey AK, Krishna S, Rawat T, Shukla PK, Maikhuri JP, Siddiqi MI, Gupta G, Sharma VL..  (2016)  Role of disulfide linkage in action of bis(dialkylaminethiocarbonyl)disulfides as potent double-Edged microbicidal spermicide: Design, synthesis and biology.,  115  [PMID:27084496] [10.1016/j.ejmech.2016.03.012]

Source