1'-[[5-(aminomethyl)-1-isopentyl-benzimidazol-2-yl]methyl]spiro[cyclopentane-1,3'-pyrrolo[2,3-c]pyridine]-2'-one

ID: ALA4877602

PubChem CID: 71528756

Max Phase: Preclinical

Molecular Formula: C25H31N5O

Molecular Weight: 417.56

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)CCn1c(CN2C(=O)C3(CCCC3)c3ccncc32)nc2cc(CN)ccc21

Standard InChI:  InChI=1S/C25H31N5O/c1-17(2)8-12-29-21-6-5-18(14-26)13-20(21)28-23(29)16-30-22-15-27-11-7-19(22)25(24(30)31)9-3-4-10-25/h5-7,11,13,15,17H,3-4,8-10,12,14,16,26H2,1-2H3

Standard InChI Key:  WTHUYZHBOIESBP-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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    7.8666   -4.6353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6905   -3.8289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8691   -3.7471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5377   -4.5031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6749   -7.8944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3913   -7.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3885   -6.6505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6731   -6.2415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9600   -7.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9567   -6.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1717   -6.4057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    9.1771   -7.7395    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1014   -6.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8174   -6.6452    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8649   -7.0779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4494   -6.3651    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9253   -8.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4799   -9.1359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2281   -9.9217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7826  -10.5324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4218  -10.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7777   -5.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6245   -6.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4518   -5.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6691   -5.2273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0586   -5.7802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2358   -6.5881    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0183   -6.8360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5840   -5.4372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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  8 15  1  0
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 18 24  1  0
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  1 26  1  0
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 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 25  1  0
 24 31  2  0
M  END

Associated Targets(non-human)

Human orthopneumovirus (392 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vero (26788 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 417.56Molecular Weight (Monoisotopic): 417.2529AlogP: 4.29#Rotatable Bonds: 6
Polar Surface Area: 77.04Molecular Species: BASEHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 9.08CX LogP: 3.29CX LogD: 1.62
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.65Np Likeness Score: -0.88

References

1. Cockerill GS, Angell RM, Bedernjak A, Chuckowree I, Fraser I, Gascon-Simorte J, Gilman MSA, Good JAD, Harland R, Johnson SM, Ludes-Meyers JH, Littler E, Lumley J, Lunn G, Mathews N, McLellan JS, Paradowski M, Peeples ME, Scott C, Tait D, Taylor G, Thom M, Thomas E, Villalonga Barber C, Ward SE, Watterson D, Williams G, Young P, Powell K..  (2021)  Discovery of Sisunatovir (RV521), an Inhibitor of Respiratory Syncytial Virus Fusion.,  64  (7.0): [PMID:33729773] [10.1021/acs.jmedchem.0c01882]

Source