ID: ALA3792410

Max Phase: Preclinical

Molecular Formula: C23H25N7O5

Molecular Weight: 479.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1c(C(O)CN2CCN(C(=O)Cc3ccc(-n4cnnn4)nc3)CC2)ccc2c1COC2=O

Standard InChI:  InChI=1S/C23H25N7O5/c1-34-22-17(4-3-16-18(22)13-35-23(16)33)19(31)12-28-6-8-29(9-7-28)21(32)10-15-2-5-20(24-11-15)30-14-25-26-27-30/h2-5,11,14,19,31H,6-10,12-13H2,1H3

Standard InChI Key:  JDZPASOANBJWRN-UHFFFAOYSA-N

Associated Targets(Human)

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

ATP-sensitive inward rectifier potassium channel 1 313 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

Properties

Molecular Weight: 479.50Molecular Weight (Monoisotopic): 479.1917AlogP: 0.16#Rotatable Bonds: 7
Polar Surface Area: 135.80Molecular Species: NEUTRALHBA: 11HBD: 1
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.38CX Basic pKa: 6.09CX LogP: 0.00CX LogD: -0.02
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.47Np Likeness Score: -1.23

References

1. Walsh SP, Shahripour A, Tang H, de Jesus RK, Teumelsan N, Zhu Y, Frie J, Priest BT, Swensen AM, Alonso-Galicia M, Felix JP, Brochu RM, Bailey T, Thomas-Fowlkes B, Zhou X, Pai LY, Hampton C, Hernandez M, Owens K, Ehrhart J, Roy S, Kaczorowski GJ, Yang L, Garcia ML, Pasternak A..  (2016)  Differentiation of ROMK potency from hERG potency in the phenacetyl piperazine series through heterocycle incorporation.,  26  (9): [PMID:27017115] [10.1016/j.bmcl.2016.03.035]

Source