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[ CAS No. 40522-46-1 ]

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Chemical Structure| 40522-46-1
Chemical Structure| 40522-46-1
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Product Details of [ 40522-46-1 ]

CAS No. :40522-46-1 MDL No. :MFCD16619170
Formula : C16H21NO Boiling Point : -
Linear Structure Formula :- InChI Key :UYRHHBXYXSYGHA-UHFFFAOYSA-N
M.W :243.34 Pubchem ID :164974
Synonyms :

Calculated chemistry of [ 40522-46-1 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.44
Num. rotatable bonds : 6
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 78.38
TPSA : 32.86 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.13
Log Po/w (XLOGP3) : 4.89
Log Po/w (WLOGP) : 4.04
Log Po/w (MLOGP) : 2.75
Log Po/w (SILICOS-IT) : 5.2
Consensus Log Po/w : 4.0

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.44
Solubility : 0.00874 mg/ml ; 0.0000359 mol/l
Class : Moderately soluble
Log S (Ali) : -5.32
Solubility : 0.00118 mg/ml ; 0.00000483 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -6.43
Solubility : 0.0000904 mg/ml ; 0.000000372 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.33

Safety of [ 40522-46-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 40522-46-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 40522-46-1 ]
  • Downstream synthetic route of [ 40522-46-1 ]

[ 40522-46-1 ] Synthesis Path-Upstream   1~17

  • 1
  • [ 111-64-8 ]
  • [ 40522-46-1 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1981, vol. 18, # 6, p. 1077 - 1079
[2] Organic and Biomolecular Chemistry, 2012, vol. 10, # 44, p. 8903 - 8910
[3] Organic and Biomolecular Chemistry, 2017, vol. 15, # 2, p. 306 - 310
[4] Angewandte Chemie - International Edition, 2017, vol. 56, # 25, p. 7271 - 7275[5] Angew. Chem., 2017, vol. 129, # 25, p. 7377 - 7381,5
[6] International Journal of Molecular Sciences, 2018, vol. 19, # 6,
  • 2
  • [ 22348-96-5 ]
  • [ 40522-46-1 ]
Reference: [1] Organic and Biomolecular Chemistry, 2012, vol. 10, # 44, p. 8903 - 8910
[2] Chemical Communications, 2016, vol. 52, # 92, p. 13440 - 13443
[3] Organic and Biomolecular Chemistry, 2017, vol. 15, # 2, p. 306 - 310
[4] Angewandte Chemie - International Edition, 2017, vol. 56, # 25, p. 7271 - 7275[5] Angew. Chem., 2017, vol. 129, # 25, p. 7377 - 7381,5
[6] Patent: EP3260445, 2017, A1,
[7] International Journal of Molecular Sciences, 2018, vol. 19, # 6,
  • 3
  • [ 13283-92-6 ]
  • [ 524-14-1 ]
  • [ 40522-46-1 ]
Reference: [1] Organic Letters, 2016, vol. 18, # 15, p. 3550 - 3553
  • 4
  • [ 13195-66-9 ]
  • [ 62-53-3 ]
  • [ 40522-46-1 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1981, vol. 18, # 6, p. 1077 - 1079
[2] Chemistry and Biology, 2012, vol. 19, # 3, p. 381 - 390
[3] European Journal of Medicinal Chemistry, 2014, vol. 79, p. 173 - 183
  • 5
  • [ 437755-74-3 ]
  • [ 40522-46-1 ]
Reference: [1] Chemistry and Biology, 2012, vol. 19, # 3, p. 381 - 390
  • 6
  • [ 103576-44-9 ]
  • [ 40522-46-1 ]
Reference: [1] Organic and Biomolecular Chemistry, 2017, vol. 15, # 2, p. 306 - 310
[2] International Journal of Molecular Sciences, 2018, vol. 19, # 6,
  • 7
  • [ 66696-81-9 ]
  • [ 40522-46-1 ]
Reference: [1] Organic and Biomolecular Chemistry, 2012, vol. 10, # 44, p. 8903 - 8910
  • 8
  • [ 42405-64-1 ]
  • [ 40522-46-1 ]
Reference: [1] Organic and Biomolecular Chemistry, 2012, vol. 10, # 44, p. 8903 - 8910
  • 9
  • [ 16662-90-1 ]
  • [ 1264-52-4 ]
  • [ 341-88-8 ]
  • [ 40522-46-1 ]
Reference: [1] Journal of Biological Chemistry, 2018, vol. 293, # 24, p. 9345 - 9357
  • 10
  • [ 13195-66-9 ]
  • [ 40522-46-1 ]
Reference: [1] Synthesis, 2007, # 10, p. 1517 - 1522
  • 11
  • [ 62-53-3 ]
  • [ 40522-46-1 ]
Reference: [1] Chemical Communications, 2016, vol. 52, # 92, p. 13440 - 13443
[2] Patent: EP3260445, 2017, A1,
  • 12
  • [ 67342-98-7 ]
  • [ 40522-46-1 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1981, vol. 18, # 6, p. 1077 - 1079
  • 13
  • [ 22348-96-5 ]
  • [ 62-53-3 ]
  • [ 40522-46-1 ]
Reference: [1] Tetrahedron Letters, 2010, vol. 51, # 45, p. 5919 - 5921
  • 14
  • [ 50411-91-1 ]
  • [ 40522-46-1 ]
Reference: [1] ChemBioChem, 2011, vol. 12, # 6, p. 850 - 853
  • 15
  • [ 50411-91-1 ]
  • [ 40522-46-1 ]
Reference: [1] ChemBioChem, 2011, vol. 12, # 6, p. 850 - 853
  • 16
  • [ 1341177-73-8 ]
  • [ 40522-46-1 ]
Reference: [1] ChemBioChem, 2011, vol. 12, # 6, p. 850 - 853
  • 17
  • [ 13283-92-6 ]
  • [ 40522-46-1 ]
Reference: [1] ChemBioChem, 2011, vol. 12, # 6, p. 850 - 853
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