1,8-Diamino-4-azanonane

ID: ALA2181336

Chembl Id: CHEMBL2181336

PubChem CID: 53363065

Max Phase: Preclinical

Molecular Formula: C8H21N3

Molecular Weight: 159.28

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: 8-MeS8-methylspermidine | 8-MeS8-methylspermidine|1,8-diamino-4-azanonane|SCHEMBL341818|CHEMBL2181336

Canonical SMILES:  CC(N)CCCNCCCN

Standard InChI:  InChI=1S/C8H21N3/c1-8(10)4-2-6-11-7-3-5-9/h8,11H,2-7,9-10H2,1H3

Standard InChI Key:  WBPWRRKPNVCJJL-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

Associated Targets(Human)

DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ODC1 Tclin Ornithine decarboxylase (70 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PAOX Tchem Polyamine oxidase (84 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMOX Tchem Spermine oxidase (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SAT1 Tbio Spermidine/spermine N(1)-acetyltransferase 1 (61 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AMD1 Tchem S-adenosylmethionine decarboxylase 1 (215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Slc26a1 Sulfate anion transporter 1 (11 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: 159.28Molecular Weight (Monoisotopic): 159.1735AlogP: 0.05#Rotatable Bonds: 7
Polar Surface Area: 64.07Molecular Species: BASEHBA: 3HBD: 3
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 10.77CX LogP: -0.73CX LogD: -7.12
Aromatic Rings: Heavy Atoms: 11QED Weighted: 0.46Np Likeness Score: 0.36

References

1. Hyvönen MT, Keinänen TA, Khomutov M, Simonian A, Weisell J, Kochetkov SN, Vepsäläinen J, Alhonen L, Khomutov AR..  (2011)  The use of novel C-methylated spermidine derivatives to investigate the regulation of polyamine metabolism.,  54  (13): [PMID:21639123] [10.1021/jm200293r]

Source