ID: ALA537210

Max Phase: Preclinical

Molecular Formula: C30H54ClN3O6

Molecular Weight: 551.77

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COCCCOc1cc(C[C@@H](C[C@H](N)[C@@H](O)C[C@H](C(=O)NCCC(=O)N(C)C)C(C)C)C(C)C)ccc1OC.Cl

Standard InChI:  InChI=1S/C30H53N3O6.ClH/c1-20(2)23(16-22-10-11-27(38-8)28(17-22)39-15-9-14-37-7)18-25(31)26(34)19-24(21(3)4)30(36)32-13-12-29(35)33(5)6;/h10-11,17,20-21,23-26,34H,9,12-16,18-19,31H2,1-8H3,(H,32,36);1H/t23-,24-,25-,26-;/m0./s1

Standard InChI Key:  USLZAJDPUWHLPQ-KRZJFFIJSA-N

Associated Targets(Human)

Renin 5251 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Renin 103 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Callithrix jacchus 111 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: 551.77Molecular Weight (Monoisotopic): 551.3934AlogP: 3.26#Rotatable Bonds: 19
Polar Surface Area: 123.35Molecular Species: BASEHBA: 7HBD: 3
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.57CX LogP: 2.47CX LogD: 0.35
Aromatic Rings: 1Heavy Atoms: 39QED Weighted: 0.23Np Likeness Score: -0.04

References

1. Maibaum J, Stutz S, Göschke R, Rigollier P, Yamaguchi Y, Cumin F, Rahuel J, Baum HP, Cohen NC, Schnell CR, Fuhrer W, Gruetter MG, Schilling W, Wood JM..  (2007)  Structural modification of the P2' position of 2,7-dialkyl-substituted 5(S)-amino-4(S)-hydroxy-8-phenyl-octanecarboxamides: the discovery of aliskiren, a potent nonpeptide human renin inhibitor active after once daily dosing in marmosets.,  50  (20): [PMID:17824680] [10.1021/jm070316i]

Source