ID: ALA2049150

Max Phase: Preclinical

Molecular Formula: C30H51N11O5

Molecular Weight: 645.81

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)[C@H](NC(=O)[C@H](CCCNC(=N)N)NCC(=O)Oc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NC1CCNCC1

Standard InChI:  InChI=1S/C30H51N11O5/c1-19(2)25(28(45)40-23(11-7-15-37-30(33)34)27(44)39-20-12-16-35-17-13-20)41-26(43)22(10-6-14-36-29(31)32)38-18-24(42)46-21-8-4-3-5-9-21/h3-5,8-9,19-20,22-23,25,35,38H,6-7,10-18H2,1-2H3,(H,39,44)(H,40,45)(H,41,43)(H4,31,32,36)(H4,33,34,37)/t22-,23-,25-/m0/s1

Standard InChI Key:  KVCZNRJJNISKEN-LSQMVHIFSA-N

Associated Targets(Human)

Furin 909 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: 645.81Molecular Weight (Monoisotopic): 645.4075AlogP: -1.43#Rotatable Bonds: 19
Polar Surface Area: 261.46Molecular Species: BASEHBA: 9HBD: 11
#RO5 Violations: 2HBA (Lipinski): 16HBD (Lipinski): 13#RO5 Violations (Lipinski): 3
CX Acidic pKa: 12.15CX Basic pKa: 11.98CX LogP: -2.35CX LogD: -9.17
Aromatic Rings: 1Heavy Atoms: 46QED Weighted: 0.03Np Likeness Score: -0.17

References

1. López-Vallejo F, Martínez-Mayorga K..  (2012)  Furin inhibitors: importance of the positive formal charge and beyond.,  20  (14): [PMID:22682919] [10.1016/j.bmc.2012.05.029]

Source