ID: ALA2426425

Max Phase: Preclinical

Molecular Formula: C29H24N4O2S2

Molecular Weight: 524.67

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CC(=O)NN(C(=S)c1ccccc1)c1ccccc1)NN(C(=S)c1ccccc1)c1ccccc1

Standard InChI:  InChI=1S/C29H24N4O2S2/c34-26(30-32(24-17-9-3-10-18-24)28(36)22-13-5-1-6-14-22)21-27(35)31-33(25-19-11-4-12-20-25)29(37)23-15-7-2-8-16-23/h1-20H,21H2,(H,30,34)(H,31,35)

Standard InChI Key:  BSVIZQTWEMFWNI-UHFFFAOYSA-N

Associated Targets(Human)

Ramos 1218 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

Properties

Molecular Weight: 524.67Molecular Weight (Monoisotopic): 524.1341AlogP: 5.20#Rotatable Bonds: 6
Polar Surface Area: 64.68Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.07CX Basic pKa: CX LogP: 6.13CX LogD: 6.13
Aromatic Rings: 4Heavy Atoms: 37QED Weighted: 0.21Np Likeness Score: -0.36

References

1. Chen S, Sun L, Koya K, Tatsuta N, Xia Z, Korbut T, Du Z, Wu J, Liang G, Jiang J, Ono M, Zhou D, Sonderfan A..  (2013)  Syntheses and antitumor activities of N'1,N'3-dialkyl-N'1,N'3-di-(alkylcarbonothioyl) malonohydrazide: the discovery of elesclomol.,  23  (18): [PMID:23937981] [10.1016/j.bmcl.2013.07.032]

Source