ID: ALA4582190

Max Phase: Preclinical

Molecular Formula: C9H21N3O

Molecular Weight: 187.29

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCCCNC(=N)NCCOC

Standard InChI:  InChI=1S/C9H21N3O/c1-3-4-5-6-11-9(10)12-7-8-13-2/h3-8H2,1-2H3,(H3,10,11,12)

Standard InChI Key:  ONGYOPVODVLOHL-UHFFFAOYSA-N

Associated Targets(Human)

N(G),N(G)-dimethylarginine dimethylaminohydrolase 1 231 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric-oxide synthase, brain 1786 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric-oxide synthase, endothelial 1452 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric oxide synthase, inducible 1636 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Arginase-1 70 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 187.29Molecular Weight (Monoisotopic): 187.1685AlogP: 0.94#Rotatable Bonds: 7
Polar Surface Area: 57.14Molecular Species: BASEHBA: 2HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 12.56CX LogP: 1.04CX LogD: -1.37
Aromatic Rings: 0Heavy Atoms: 13QED Weighted: 0.32Np Likeness Score: -0.32

References

1. Lunk I, Litty FA, Hennig S, Vetter IR, Kotthaus J, Altmann KS, Ott G, Havemeyer A, Carrillo García C, Clement B, Schade D..  (2020)  Discovery of N-(4-Aminobutyl)-N'-(2-methoxyethyl)guanidine as the First Selective, Nonamino Acid, Catalytic Site Inhibitor of Human Dimethylarginine Dimethylaminohydrolase-1 (hDDAH-1).,  63  (1): [PMID:31841335] [10.1021/acs.jmedchem.9b01230]

Source