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[ CAS No. 67-03-8 ] {[proInfo.proName]}

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Chemical Structure| 67-03-8
Chemical Structure| 67-03-8
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Product Citations

Product Citations

Cole, Presley C ; Martinez, Briana I ; Shell, Thomas A DOI:

Abstract: (PHT, brand name: Dilantin) is an anticonvulsant drug that is used in the treatment of epilepsy. PHT is metabolically inactivated by cytochromes P-450 (CYP) catalyzed aromatic hydroxylation at the para position. Therefore, Nelson et al. hypothesized that this metabolic pathway would be slowed or blocked for a PHT derivative with fluorines at the para positions of the aromatic rings (pF-PHT) resulting in a molecule with increased antiseizure activity and longer duration of action relative to PHT. Interestingly, pF-PHT is less active than PHT, but has a much longer duration of action. Nelson et al. hypothesized that differences in physicochemical properties must contribute to the poor activity of pF-PHT. Thus, pF-PHT was synthesized to compare its physicochemical properties with those of PHT. In addition, the kinetics of CYP catalyzed oxidation were compared using Sprague Dawley (SD) rat liver microsomes because PHT is metabolically inactivated by CYP in the liver. The previously reported synthesis of pF-PHT employs a highly toxic reagent and produces a highly poisonous gas. Therefore, a safer synthetic route for pF-PHT was developed. This synthetic approach utilizes three steps: 1) a thiamine catalyzed condensation of , 2) a nitric acid oxidation of the product to the corresponding derivative, and 3) a microwave-assisted synthesis of this derivative with urea. There are no significant differences in conjugation, acidity, and lipophilicity between PHT and pF-PHT. Therefore, our results do not support the hypothesis that the low activity of pF-PHT relative to PHT results from variations in physicochemical properties. While PHT and pF-PHT have the same apparent binding affinity for the CYP proteome of the SD rat liver microsome, pF-PHT undergoes CYP catalyzed oxidation at half the rate in comparison to PHT.

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Product Details of [ 67-03-8 ]

CAS No. :67-03-8 MDL No. :MFCD00012780
Formula : C12H18Cl2N4OS Boiling Point : -
Linear Structure Formula :- InChI Key :DPJRMOMPQZCRJU-UHFFFAOYSA-M
M.W : 337.27 Pubchem ID :6202
Synonyms :
Thiamine chloride hydrochloride;Vitamin B1 hydrochloride;Aneurine;Thiamine (hydrochloride);Vitamin B1;Thiamine HCl
Chemical Name :3-((4-Amino-2-methylpyrimidin-5-yl)methyl)-5-(2-hydroxyethyl)-4-methylthiazol-3-ium chloride hydrochloride

Calculated chemistry of [ 67-03-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.42
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 86.08
TPSA : 104.15 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.63
Log Po/w (WLOGP) : -1.58
Log Po/w (MLOGP) : 0.58
Log Po/w (SILICOS-IT) : 2.54
Consensus Log Po/w : 0.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.73
Solubility : 0.0627 mg/ml ; 0.000186 mol/l
Class : Soluble
Log S (Ali) : -4.47
Solubility : 0.0115 mg/ml ; 0.0000341 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.3
Solubility : 0.168 mg/ml ; 0.000499 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.09

Safety of [ 67-03-8 ]

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