3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(4-methylpiperazin-1-yl)-1H-isochromen-1-one

ID: ALA4079209

PubChem CID: 71652160

Max Phase: Preclinical

Molecular Formula: C22H23N5O2

Molecular Weight: 389.46

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1cn2cc(-c3cc4ccc(N5CCN(C)CC5)cc4c(=O)o3)nc2c(C)n1

Standard InChI:  InChI=1S/C22H23N5O2/c1-14-12-27-13-19(24-21(27)15(2)23-14)20-10-16-4-5-17(11-18(16)22(28)29-20)26-8-6-25(3)7-9-26/h4-5,10-13H,6-9H2,1-3H3

Standard InChI Key:  IJTUIAVNGJAVKK-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

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    6.6622   -5.7918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3832   -5.3787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9461   -5.3736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5318   -4.5367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3706   -6.5878    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0848   -7.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.1774   -3.3193    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9856   -3.1409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3952   -3.8562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.2181   -3.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6323   -3.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2136   -2.4295    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.3920   -2.4332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9782   -1.7180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4591   -3.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
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M  END

Associated Targets(non-human)

Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 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: 389.46Molecular Weight (Monoisotopic): 389.1852AlogP: 2.87#Rotatable Bonds: 2
Polar Surface Area: 66.88Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 7.66CX LogP: 1.52CX LogD: 1.08
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.53Np Likeness Score: -0.94

References

1. Pinard E, Green L, Reutlinger M, Weetall M, Naryshkin NA, Baird J, Chen KS, Paushkin SV, Metzger F, Ratni H..  (2017)  Discovery of a Novel Class of Survival Motor Neuron 2 Splicing Modifiers for the Treatment of Spinal Muscular Atrophy.,  60  (10): [PMID:28441483] [10.1021/acs.jmedchem.7b00406]
2. Ratni H, Karp GM, Weetall M, Naryshkin NA, Paushkin SV, Chen KS, McCarthy KD, Qi H, Turpoff A, Woll MG, Zhang X, Zhang N, Yang T, Dakka A, Vazirani P, Zhao X, Pinard E, Green L, David-Pierson P, Tuerck D, Poirier A, Muster W, Kirchner S, Mueller L, Gerlach I, Metzger F..  (2016)  Specific Correction of Alternative Survival Motor Neuron 2 Splicing by Small Molecules: Discovery of a Potential Novel Medicine To Treat Spinal Muscular Atrophy.,  59  (13): [PMID:27299419] [10.1021/acs.jmedchem.6b00459]
3. Woll MG, Qi H, Turpoff A, Zhang N, Zhang X, Chen G, Li C, Huang S, Yang T, Moon YC, Lee CS, Choi S, Almstead NG, Naryshkin NA, Dakka A, Narasimhan J, Gabbeta V, Welch E, Zhao X, Risher N, Sheedy J, Weetall M, Karp GM..  (2016)  Discovery and Optimization of Small Molecule Splicing Modifiers of Survival Motor Neuron 2 as a Treatment for Spinal Muscular Atrophy.,  59  (13): [PMID:27299569] [10.1021/acs.jmedchem.6b00460]

Source