ID: ALA2426428

Max Phase: Preclinical

Molecular Formula: C25H28N4O6S2

Molecular Weight: 544.66

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C25H28N4O6S2/c30-20(26-28(18-9-3-1-4-10-18)22(36)13-7-15-24(32)33)17-21(31)27-29(19-11-5-2-6-12-19)23(37)14-8-16-25(34)35/h1-6,9-12H,7-8,13-17H2,(H,26,30)(H,27,31)(H,32,33)(H,34,35)

Standard InChI Key:  GOIGVRQQFWCVCO-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: 544.66Molecular Weight (Monoisotopic): 544.1450AlogP: 3.62#Rotatable Bonds: 12
Polar Surface Area: 139.28Molecular Species: ACIDHBA: 6HBD: 4
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.07CX Basic pKa: CX LogP: 2.96CX LogD: -2.86
Aromatic Rings: 2Heavy Atoms: 37QED Weighted: 0.18Np Likeness Score: -0.23

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