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[ CAS No. 1402727-29-0 ] {[proInfo.proName]}

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Chemical Structure| 1402727-29-0
Chemical Structure| 1402727-29-0
Structure of 1402727-29-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1402727-29-0 ]

CAS No. :1402727-29-0 MDL No. :MFCD28411710
Formula : C28H24N4O2 Boiling Point : -
Linear Structure Formula :- InChI Key :AMBZHNVCLPHAKA-NSJFVGFPSA-N
M.W : 448.52 Pubchem ID :66571561
Synonyms :

Calculated chemistry of [ 1402727-29-0 ]

Physicochemical Properties

Num. heavy atoms : 34
Num. arom. heavy atoms : 26
Fraction Csp3 : 0.07
Num. rotatable bonds : 8
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 136.45
TPSA : 75.82 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.56
Log Po/w (XLOGP3) : 5.35
Log Po/w (WLOGP) : 5.63
Log Po/w (MLOGP) : 2.7
Log Po/w (SILICOS-IT) : 6.71
Consensus Log Po/w : 4.79

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -6.03
Solubility : 0.000419 mg/ml ; 0.000000935 mol/l
Class : Poorly soluble
Log S (Ali) : -6.7
Solubility : 0.0000905 mg/ml ; 0.000000202 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -9.63
Solubility : 0.000000105 mg/ml ; 0.0000000002 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 3.56

Safety of [ 1402727-29-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1402727-29-0 ]

* 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 [ 1402727-29-0 ]
  • Downstream synthetic route of [ 1402727-29-0 ]

[ 1402727-29-0 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 1402728-56-6 ]
  • [ 1402727-29-0 ]
YieldReaction ConditionsOperation in experiment
75% at 20 - 60℃; for 3 h; Compound 3e (400 mg, 0.898 mmol) was dissolved in 4.5 mL of acetic acid. After hydrazine monohydrate (0.45 g, 9.0 mmol) was added at room temperature, the mixture was stirred at 60 °C for 3 hours. The resulting mixture was diluted with AcOEt, washed with saturated aqueous solutions of NaHCO3, saturated brine, and dried over MgSO4. After filtration, the solvent was evaporated under reduced pressure. The residue was chromatographed on silica gel (hexane/AcOEt system or CHCl3/MeOH system) to yield the title compound as a pale yellowish white powder (298 mg) in 75percent yield. 1H NMR (δ, acetone-d6): 3.92 (s, 3H), 5.24 (s, 2H), 6.47 (br d, J = 3 Hz, 1H), 6.67 (dd, J = 2.2, 8.5 Hz, 1H), 6.70 (s, 1H), 6.75 (d, J = 2.2 Hz, 1H), 7.07 (d, J = 17 Hz, 1H), 7.11 (d, J = 17 Hz, 1H), 7.32 (d, J = 17 Hz, 1H), 7.30~7.38 (m, 3H), 7.39 (d, J = 17 Hz, 1H), 7.54 (d, J = 8.3 Hz, 1H), 7.55~7.59 (m, 2H), 7.59 (br s, 1H), 7.84 (dt, J = 1.7, 7.7 Hz, 1H), 8.60 (br d, J = 5 Hz, 1H), 10.3 (br s, NH). 13C NMR (δ, DMSO-d6): 159.4, 157.9, 156.8, 149.3, 137.2, 136.5, 131.2, 130.2, 127.9, 127.7, 126.6, 124.0, 123.2, 122.0, 120.6, 118.7, 117.5, 110.3, 106.6, 101.6, 99.6, 99.5, 70.7, 55.8. mp: 237–239°C, MS (ESI+) m/z 449.2 (M+1), HRMS (ESI) calcd for C28H25N4O2 ([M+H]+): 449.1972; found: 449.1974.
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 20, p. 5024 - 5028
  • 2
  • [ 1196-70-9 ]
  • [ 1402727-29-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 20, p. 5024 - 5028
  • 3
  • [ 123-54-6 ]
  • [ 1402727-29-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 20, p. 5024 - 5028
  • 4
  • [ 1151539-21-7 ]
  • [ 1402727-29-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 20, p. 5024 - 5028
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