Dihydromotuporamine C trihydrochloride

ID: ALA4093452

Chembl Id: CHEMBL4093452

PubChem CID: 137656078

Max Phase: Preclinical

Molecular Formula: C20H46Cl3N3

Molecular Weight: 325.59

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cl.Cl.Cl.NCCCNCCCN1CCCCCCCCCCCCCC1

Standard InChI:  InChI=1S/C20H43N3.3ClH/c21-15-13-16-22-17-14-20-23-18-11-9-7-5-3-1-2-4-6-8-10-12-19-23;;;/h22H,1-21H2;3*1H

Standard InChI Key:  VTNIDUZFSFCWSX-UHFFFAOYSA-N

Associated Targets(non-human)

CHO-MG (239 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

Calculated Properties

Molecular Weight: 325.59Molecular Weight (Monoisotopic): 325.3457AlogP: 4.31#Rotatable Bonds: 7
Polar Surface Area: 41.29Molecular Species: BASEHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 10.59CX LogP: 4.00CX LogD: -1.23
Aromatic Rings: Heavy Atoms: 23QED Weighted: 0.69Np Likeness Score: -0.48

References

1. Skruber K, Chaplin KJ, Phanstiel O..  (2017)  Synthesis and Bioevaluation of Macrocycle-Polyamine Conjugates as Cell Migration Inhibitors.,  60  (20): [PMID:28976754] [10.1021/acs.jmedchem.7b01222]

Source