N-Ethyl-N'-{4-[4-(4-ethylamino-but-2-enylamino)-butylamino]-butyl}-but-2-ene-1,4-diamine; 5M HCl

ID: ALA1237413

Chembl Id: CHEMBL1237413

PubChem CID: 52946634

Max Phase: Preclinical

Molecular Formula: C20H48Cl5N5

Molecular Weight: 353.60

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: CGC-11128 | CHEMBL1237413|CGC-11128

Canonical SMILES:  CCNC/C=C\CNCCCCNCCCCNC/C=C\CNCC.Cl.Cl.Cl.Cl.Cl

Standard InChI:  InChI=1S/C20H43N5.5ClH/c1-3-21-13-5-7-15-23-17-9-11-19-25-20-12-10-18-24-16-8-6-14-22-4-2;;;;;/h5-8,21-25H,3-4,9-20H2,1-2H3;5*1H/b7-5-,8-6-;;;;;

Standard InChI Key:  ALPMHBAKCRSQET-NMMBYFETSA-N

Associated Targets(Human)

LNCaP (8286 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DuPro (144 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 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: 353.60Molecular Weight (Monoisotopic): 353.3518AlogP: 1.65#Rotatable Bonds: 20
Polar Surface Area: 60.15Molecular Species: BASEHBA: 5HBD: 5
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 10.93CX LogP: 1.27CX LogD: -11.29
Aromatic Rings: Heavy Atoms: 25QED Weighted: 0.17Np Likeness Score: -0.01

References

1. Reddy VK, Sarkar A, Valasinas A, Marton LJ, Basu HS, Frydman B..  (2001)  cis-Unsaturated analogues of 3,8,13,18,23-pentaazapentacosane (BE-4-4-4-4): synthesis and growth inhibitory effects on human prostate cancer cell lines.,  44  (3): [PMID:11462980] [10.1021/jm000310s]
2. Casero RA, Woster PM..  (2009)  Recent advances in the development of polyamine analogues as antitumor agents.,  52  (15): [PMID:19534534] [10.1021/jm900187v]

Source