ID: ALA4299212

Max Phase: Preclinical

Molecular Formula: C26H45N11O6S2

Molecular Weight: 570.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(CC)CC.Nc1ncnc2c1ncn2[C@@H]1O[C@H](CNS(=O)(=O)NC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@@H]32)[C@@H](O)[C@H]1N

Standard InChI:  InChI=1S/C20H30N10O6S2.C6H15N/c21-13-16(32)10(36-19(13)30-8-25-15-17(22)23-7-24-18(15)30)5-26-38(34,35)29-12(31)4-2-1-3-11-14-9(6-37-11)27-20(33)28-14;1-4-7(5-2)6-3/h7-11,13-14,16,19,26,32H,1-6,21H2,(H,29,31)(H2,22,23,24)(H2,27,28,33);4-6H2,1-3H3/t9-,10+,11-,13+,14-,16+,19+;/m0./s1

Standard InChI Key:  NVCFATWBAAQDQA-XCWKCCEMSA-N

Associated Targets(non-human)

Biotin--acetyl-CoA-carboxylase ligase 26 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium tuberculosis 203094 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: 570.66Molecular Weight (Monoisotopic): 570.1791AlogP: -2.33#Rotatable Bonds: 10
Polar Surface Area: 241.50Molecular Species: ZWITTERIONHBA: 13HBD: 7
#RO5 Violations: 3HBA (Lipinski): 16HBD (Lipinski): 9#RO5 Violations (Lipinski): 3
CX Acidic pKa: 4.14CX Basic pKa: 8.63CX LogP: -3.80CX LogD: -3.80
Aromatic Rings: 2Heavy Atoms: 38QED Weighted: 0.12Np Likeness Score: 0.01

References

1. Bockman MR, Kalinda AS, Petrelli R, De la Mora-Rey T, Tiwari D, Liu F, Dawadi S, Nandakumar M, Rhee KY, Schnappinger D, Finzel BC, Aldrich CC..  (2015)  Targeting Mycobacterium tuberculosis Biotin Protein Ligase (MtBPL) with Nucleoside-Based Bisubstrate Adenylation Inhibitors.,  58  (18): [PMID:26299766] [10.1021/acs.jmedchem.5b00719]

Source