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[ CAS No. 16382-18-6 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 16382-18-6
Chemical Structure| 16382-18-6
Chemical Structure| 16382-18-6
Structure of 16382-18-6 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 16382-18-6 ]

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Product Details of [ 16382-18-6 ]

CAS No. :16382-18-6 MDL No. :MFCD00015457
Formula : C13H15NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :RBUSDPZPBBBAKR-UHFFFAOYSA-N
M.W : 249.26 Pubchem ID :85385
Synonyms :

Calculated chemistry of [ 16382-18-6 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.31
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 67.37
TPSA : 60.55 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) : -6.02 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.59
Log Po/w (XLOGP3) : 2.54
Log Po/w (WLOGP) : 2.36
Log Po/w (MLOGP) : 1.08
Log Po/w (SILICOS-IT) : 2.78
Consensus Log Po/w : 2.27

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.03
Solubility : 0.235 mg/ml ; 0.000943 mol/l
Class : Soluble
Log S (Ali) : -3.46
Solubility : 0.0867 mg/ml ; 0.000348 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.03
Solubility : 0.0235 mg/ml ; 0.0000942 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.11

Safety of [ 16382-18-6 ]

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 [ 16382-18-6 ]

* 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 [ 16382-18-6 ]
  • Downstream synthetic route of [ 16382-18-6 ]

[ 16382-18-6 ] Synthesis Path-Upstream   1~12

  • 1
  • [ 16382-18-6 ]
  • [ 4790-08-3 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 7, p. 550 - 554
  • 2
  • [ 2999-46-4 ]
  • [ 5392-10-9 ]
  • [ 16382-18-6 ]
Reference: [1] Chemical Communications, 2009, # 48, p. 7581 - 7583
[2] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 7, p. 550 - 554
  • 3
  • [ 5392-10-9 ]
  • [ 623-33-6 ]
  • [ 16382-18-6 ]
Reference: [1] European Journal of Organic Chemistry, 2014, vol. 2014, # 3, p. 511 - 514
[2] European Journal of Organic Chemistry, 2014, vol. 2014, # 3, p. 511 - 514
  • 4
  • [ 1906-82-7 ]
  • [ 5392-10-9 ]
  • [ 16382-18-6 ]
Reference: [1] Tetrahedron Letters, 2010, vol. 51, # 50, p. 6549 - 6551
  • 5
  • [ 91958-71-3 ]
  • [ 16382-18-6 ]
Reference: [1] Synthesis, 1984, vol. NO. 10, p. 862 - 865
  • 6
  • [ 1016-58-6 ]
  • [ 16382-18-6 ]
Reference: [1] Organic and Biomolecular Chemistry, 2015, vol. 13, # 9, p. 2588 - 2599
  • 7
  • [ 53413-67-5 ]
  • [ 16382-18-6 ]
Reference: [1] Organic and Biomolecular Chemistry, 2015, vol. 13, # 9, p. 2588 - 2599
  • 8
  • [ 86323-64-0 ]
  • [ 16382-18-6 ]
Reference: [1] Synlett, 2006, # 5, p. 749 - 755
  • 9
  • [ 6315-89-5 ]
  • [ 16382-18-6 ]
Reference: [1] Synlett, 2006, # 5, p. 749 - 755
  • 10
  • [ 120-14-9 ]
  • [ 16382-18-6 ]
Reference: [1] Archives of Pharmacal Research, 2011, vol. 34, # 3, p. 357 - 367
  • 11
  • [ 911301-33-2 ]
  • [ 16382-18-6 ]
Reference: [1] Archives of Pharmacal Research, 2011, vol. 34, # 3, p. 357 - 367
  • 12
  • [ 16382-18-6 ]
  • [ 126434-73-9 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 7, p. 550 - 554
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