(+/-)-2'-benzyl-S-adenosylmethionine iodide

ID: ALA1933121

Chembl Id: CHEMBL1933121

PubChem CID: 56648141

Max Phase: Preclinical

Molecular Formula: C22H29IN6O5S

Molecular Weight: 489.58

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C[S+](CC[C@H](N)C(=O)O)C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](OCc2ccccc2)[C@@H]1O.[I-]

Standard InChI:  InChI=1S/C22H28N6O5S.HI/c1-34(8-7-14(23)22(30)31)10-15-17(29)18(32-9-13-5-3-2-4-6-13)21(33-15)28-12-27-16-19(24)25-11-26-20(16)28;/h2-6,11-12,14-15,17-18,21,29H,7-10,23H2,1H3,(H2-,24,25,26,30,31);1H/t14-,15+,17+,18+,21+,34?;/m0./s1

Standard InChI Key:  ARSXGZALHGYHTM-LXPLAMTJSA-N

Associated Targets(non-human)

A612L Histone H3K27 methylase (21 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: 489.58Molecular Weight (Monoisotopic): 489.1915AlogP: 0.30#Rotatable Bonds: 10
Polar Surface Area: 171.63Molecular Species: ZWITTERIONHBA: 10HBD: 4
#RO5 Violations: HBA (Lipinski): 11HBD (Lipinski): 6#RO5 Violations (Lipinski): 2
CX Acidic pKa: 1.71CX Basic pKa: 9.41CX LogP: -2.95CX LogD: -2.96
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.29Np Likeness Score: 0.86

References

1. Li J, Wei H, Zhou MM..  (2011)  Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.,  54  (21): [PMID:21958314] [10.1021/jm201000j]

Source