ID: ALA4544147

Max Phase: Preclinical

Molecular Formula: C9H20N4

Molecular Weight: 184.29

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=CCCNC(=N)NCCCCN

Standard InChI:  InChI=1S/C9H20N4/c1-2-3-7-12-9(11)13-8-5-4-6-10/h2H,1,3-8,10H2,(H3,11,12,13)

Standard InChI Key:  AKRJZJHGIJJBLM-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: 184.29Molecular Weight (Monoisotopic): 184.1688AlogP: 0.42#Rotatable Bonds: 7
Polar Surface Area: 73.93Molecular Species: BASEHBA: 2HBD: 4
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 12.89CX LogP: 0.12CX LogD: -4.60
Aromatic Rings: 0Heavy Atoms: 13QED Weighted: 0.20Np Likeness Score: 0.76

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