CAS 86150-61-0

Valacyclovir Related Compound F (2-hydroxyethyl valinate para-toluenesulfonate salt)

CAS: 86150-61-0

Non-aromatic amino-compounds with oxygen function

Formel: C₇H₁₅NO₃·C₇H₈O₃S

Farbe und Form: White Off-White Powder

Molekulargewicht: 161.10519

Ref: 45-1707883

(S)-2-Hydroxyethyl 2-amino-3-methylbutanoate 4-methylbenzenesulfonate

CAS: 86150-61-0

Formel: C₁₄H₂₃NO₆S

Reinheit: 95%

Farbe und Form: Solid

Molekulargewicht: 333.4005

Ref: IN-DA003RDY

(S)-2-Hydroxyethyl 2-amino-3-methylbutanoate 4-methylbenzenesulfonate

CAS: 86150-61-0

(S)-2-Hydroxyethyl 2-amino-3-methylbutanoate 4-methylbenzenesulfonate

Reinheit: 95%

Molekulargewicht: 333.41g/mol

Ref: 54-OR1045908

Valaciclovir EP Impurity F Tosylate (Valacyclovir USP Related Compound F)

CAS: 86150-61-0

Formel: C₇H₁₅NO₃·C₇H₈O₃S

Farbe und Form: White To Off-White Solid

Molekulargewicht: 161.20 172.20

Ref: 4Z-V-016

2-Hydroxyethyl L-Valinate para-Toluenesulfonate

CAS: 86150-61-0

Farbe und Form: Off White Solid

Ref: 86-MM0619.19

L-Valine 2-Hydroxyethyl Ester Tosylate

Kontrolliertes Produkt

CAS: 86150-61-0

Impurity Valaciclovir EP Impurity F; Valacyclovir USP Related Compound F
Applications L-Valine 2-Hydroxyethyl Ester Tosylate is a L-Valacyclovir Hydrochloride (V085000) related compound F, which is the L-Valine ester prodrug of Acyclovir.
References Beauchamp, L.M., et al.: Antiviral Chem. Chemother., 3, 157 (1992), Weller, S., et al.: Clin. Pharmacol. Ther., 54, 595 (1996), Lowance, D., et al.: N. Engl. J. Med., 340, 1462 (1999)

Formel: C₇H₁₅NO₃·C₇H₈O₃S

Farbe und Form: Neat

Molekulargewicht: 333.4

Ref: TR-V094320

Valaciclovir EP Impurity F

CAS: 86150-61-0

Formel: C₇H₁₅NO₃C₇H₈O₃S

Molekulargewicht: 161.20 : 172.20

Ref: ST-EA-CP-V4006

L-Valine 2-hydroxyethyl ester tosylate

CAS: 86150-61-0

L-Valine 2-hydroxyethyl ester tosylate (L-V2HT) is a drug product that is synthesized by custom synthesis. It has high purity, analytical, and natural properties. L-V2HT is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. The active form of L-V2HT is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. L-V2HT also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell

Formel: C₁₄H₂₃NO₆S

Reinheit: Min. 95%

Molekulargewicht: 333.4 g/mol

Ref: 3D-IV178763