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[ CAS No. 152626-75-0 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 152626-75-0
Chemical Structure| 152626-75-0
Chemical Structure| 152626-75-0
Structure of 152626-75-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 152626-75-0 ]

CAS No. :152626-75-0 MDL No. :MFCD11007881
Formula : C8H7N3O3 Boiling Point : -
Linear Structure Formula :- InChI Key :QULAONDBWZZTOI-UHFFFAOYSA-N
M.W : 193.16 Pubchem ID :15278630
Synonyms :

Calculated chemistry of [ 152626-75-0 ]

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.41
TPSA : 83.73 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.68
Log Po/w (XLOGP3) : 1.35
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 0.63
Log Po/w (SILICOS-IT) : -0.2
Consensus Log Po/w : 0.79

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.23
Solubility : 1.13 mg/ml ; 0.00586 mol/l
Class : Soluble
Log S (Ali) : -2.71
Solubility : 0.376 mg/ml ; 0.00195 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.42
Solubility : 0.729 mg/ml ; 0.00378 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.08

Safety of [ 152626-75-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 152626-75-0 ]

* 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 [ 152626-75-0 ]
  • Downstream synthetic route of [ 152626-75-0 ]

[ 152626-75-0 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 152626-75-0 ]
  • [ 749223-61-8 ]
Reference: [1] Journal of the Chemical Society, 1955, p. 2412,2419
[2] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2115 - 2137
[3] Patent: US2012/15962, 2012, A1, . Location in patent: Page/Page column 90
  • 2
  • [ 361162-90-5 ]
  • [ 152626-75-0 ]
Reference: [1] Patent: US2012/15962, 2012, A1, . Location in patent: Page/Page column 89-90
  • 3
  • [ 3522-07-4 ]
  • [ 152626-75-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2115 - 2137
  • 4
  • [ 50868-72-9 ]
  • [ 152626-75-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2115 - 2137
[2] Patent: US2012/15962, 2012, A1,
  • 5
  • [ 343773-70-6 ]
  • [ 152626-75-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2115 - 2137
  • 6
  • [ 50868-75-2 ]
  • [ 152626-75-0 ]
Reference: [1] Patent: US2012/15962, 2012, A1,
  • 7
  • [ 106579-00-4 ]
  • [ 152626-75-0 ]
Reference: [1] Journal of the Chemical Society, 1955, p. 2412,2419
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