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[ CAS No. 179873-45-1 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 179873-45-1
Chemical Structure| 179873-45-1
Chemical Structure| 179873-45-1
Structure of 179873-45-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 179873-45-1 ]

CAS No. :179873-45-1 MDL No. :MFCD07772795
Formula : C11H13N3 Boiling Point : -
Linear Structure Formula :- InChI Key :VZIBQMZVUZDSFA-UHFFFAOYSA-N
M.W : 187.24 Pubchem ID :7157371
Synonyms :

Calculated chemistry of [ 179873-45-1 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.18
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 56.14
TPSA : 29.85 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.12
Log Po/w (XLOGP3) : 1.04
Log Po/w (WLOGP) : 1.44
Log Po/w (MLOGP) : 1.04
Log Po/w (SILICOS-IT) : 1.51
Consensus Log Po/w : 1.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.04
Solubility : 1.71 mg/ml ; 0.00913 mol/l
Class : Soluble
Log S (Ali) : -1.26
Solubility : 10.4 mg/ml ; 0.0553 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.77
Solubility : 0.0317 mg/ml ; 0.000169 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.39

Safety of [ 179873-45-1 ]

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

Application In Synthesis of [ 179873-45-1 ]

* 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.

  • Downstream synthetic route of [ 179873-45-1 ]

[ 179873-45-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [(1-benzyl-1H-benzoimidazole-carbonyl)-amino]-acetic acid [ No CAS ]
  • [ 179873-45-1 ]
  • 1-benzyl-N-(2-[4-(1H-imidazol-1-yl)benzyl](methyl)amino}-2-oxoethyl)-1H-benzimidazole-2-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
96% With 2-chloro-1,3-dimethylimidazolinium chloride; N-ethyl-N,N-diisopropylamine In acetonitrile
  • 2
  • [ 179873-45-1 ]
  • C19H21N3O5S [ No CAS ]
  • [ 1211569-97-9 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran at 20℃; for 72h; 2 5-([(4-Methoxy-2,6-dimethylphenyl)sulfonyl](methyl)amino}methyl)furan-3-carboxylic acid (74 mg, 0.21 mmol) is dissolved in THF (4 mL) and CDI (68 mg, 0.42 mmol) added. The resulting solution was stirred for 90 min prior to the addition of l-(l-methylpiperidin-4- yl)piperazine (77 mg, 0.42 mmol). The reaction was stirred at ambient temperature for 18 h, concentrated in vacuo and a portion of the resulting crude product purified using prep methodB to afford the title compound.LCMS Method C: rt 2.65 min, 96 %; m/z 519.46.10 (MH+, 100%).Potency: A
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