(2S,3S)-3-Isopropyl-N-(3-methoxy-4-(oxazol-5-yl)phenyl)-piperidine-2-carboxamide

ID: ALA4869558

PubChem CID: 164622894

Max Phase: Preclinical

Molecular Formula: C19H25N3O3

Molecular Weight: 343.43

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(NC(=O)[C@H]2NCCC[C@H]2C(C)C)ccc1-c1cnco1

Standard InChI:  InChI=1S/C19H25N3O3/c1-12(2)14-5-4-8-21-18(14)19(23)22-13-6-7-15(16(9-13)24-3)17-10-20-11-25-17/h6-7,9-12,14,18,21H,4-5,8H2,1-3H3,(H,22,23)/t14-,18-/m0/s1

Standard InChI Key:  OIIKHSCLQXVMOG-KSSFIOAISA-N

Molfile:  

 
     RDKit          2D

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   23.9530   -8.0728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9519   -8.8924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6599   -9.3013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3696   -8.8919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3667   -8.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6581   -7.6640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2452   -7.6652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1595   -6.8525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.3602   -6.6828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9517   -7.3906    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.4987   -7.9977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2438   -9.3004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.5365   -8.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0779   -9.2994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   26.7850   -8.8897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4933   -9.2971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.7837   -8.0725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.4906  -10.1124    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   28.1949  -10.5198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9044  -10.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9051   -9.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1963   -8.8835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1940   -8.0663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9006   -7.6558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4852   -7.6597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11  7  2  0
  1  7  1  0
  2 12  1  0
 12 13  1  0
  4 14  1  0
 14 15  1  0
 16 15  1  6
 15 17  2  0
 16 18  1  0
 16 22  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 23 24  1  0
 23 25  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4869558

    ---

Associated Targets(Human)

AAK1 Tchem Adaptor-associated kinase (1053 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: 343.43Molecular Weight (Monoisotopic): 343.1896AlogP: 3.31#Rotatable Bonds: 5
Polar Surface Area: 76.39Molecular Species: BASEHBA: 5HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 12.74CX Basic pKa: 8.72CX LogP: 2.23CX LogD: 0.89
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.87Np Likeness Score: -0.28

References

1. Hartz RA, Ahuja VT, Nara SJ, Kumar CMV, Brown JM, Bristow LJ, Rajamani R, Muckelbauer JK, Camac D, Kiefer SE, Hunihan L, Gulianello M, Lewis M, Easton A, Lippy JS, Surti N, Pattipati SN, Dokania M, Elavazhagan S, Dandapani K, Hamman BD, Allen J, Kostich W, Bronson JJ, Macor JE, Dzierba CD..  (2021)  Discovery, Structure-Activity Relationships, and In Vivo Evaluation of Novel Aryl Amides as Brain Penetrant Adaptor Protein 2-Associated Kinase 1 (AAK1) Inhibitors for the Treatment of Neuropathic Pain.,  64  (15.0): [PMID:34270254] [10.1021/acs.jmedchem.1c00472]
2. Zarrinkar, Patrick P PP and 15 more authors.  2009-10-01  AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML).  [PMID:19654408]
3. and Abdel-Magid, Ahmed F AF.  2017-06-08  Inhibitors of Adaptor-Associated Kinase 1 (AAK1) May Treat Neuropathic Pain, Schizophrenia, Parkinson's Disease, and Other Disorders.  [PMID:28626516]
4. Klaeger, Susan S and 47 more authors.  2017-12-01  The target landscape of clinical kinase drugs.  [PMID:29191878]

Source