7-N-Chloroacetyldemethyllavendamycin amide

ID: ALA597805

Chembl Id: CHEMBL597805

PubChem CID: 46228801

Max Phase: Preclinical

Molecular Formula: C23H14ClN5O4

Molecular Weight: 459.85

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: 7-N-Chloroacetyldemethyllavendamycin Amide | CHEMBL597805|7-N-Chloroacetyldemethyllavendamycin amide

Canonical SMILES:  NC(=O)c1cc2c([nH]c3ccccc32)c(-c2ccc3c(n2)C(=O)C(NC(=O)CCl)=CC3=O)n1

Standard InChI:  InChI=1S/C23H14ClN5O4/c24-9-18(31)26-15-8-17(30)11-5-6-14(28-20(11)22(15)32)21-19-12(7-16(29-21)23(25)33)10-3-1-2-4-13(10)27-19/h1-8,27H,9H2,(H2,25,33)(H,26,31)

Standard InChI Key:  MCROMNREUDIJJT-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

NQO1 Tchem Quinone reductase 1 (1746 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BE (127 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: 459.85Molecular Weight (Monoisotopic): 459.0734AlogP: 2.49#Rotatable Bonds: 4
Polar Surface Area: 147.90Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 11.76CX Basic pKa: 0.51CX LogP: 1.42CX LogD: 1.42
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.40Np Likeness Score: 0.15

References

1. Cai W, Hassani M, Karki R, Walter ED, Koelsch KH, Seradj H, Lineswala JP, Mirzaei H, York JS, Olang F, Sedighi M, Lucas JS, Eads TJ, Rose AS, Charkhzarrin S, Hermann NG, Beall HD, Behforouz M..  (2010)  Synthesis, metabolism and in vitro cytotoxicity studies on novel lavendamycin antitumor agents.,  18  (5): [PMID:20149966] [10.1016/j.bmc.2010.01.037]

Source