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| Product | Description | |
|---|---|---|
| L-Valine ethyl ester hydrochloride | Synonyms: L-Val-OEt HCl; Ethyl L-valinate hydrochloride; (L)-Ethyl 2-Amino-3-mEthylbutanoate Hydrochloride; L-Valine methyl ester hydrochloride. Grades: ≥ 99% (HPLC). CAS No. 17609-47-1. Molecular formula: C7H15NO2·HCl. Mole weight: 181.65. |  |
| L-Valine ethyl ester hydrochloride 99+% | L-Valine ethyl ester hydrochloride 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g. US Biological Life Sciences. |  Worldwide |
| Valacyclovir-d4, Hydrochloride (L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Ester-d4, Hydrochlroride Salt, ValACV) | The labeled L-Valine ester prodrug of Acyclovir. Group: Biochemicals. Alternative Names: L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Ester-d4, Hydrochlroride Salt, ValACV. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Valacyclovir Hydrochloride Hydrate (L-Valine 2-(2-Amino-1,6-dihydro-6-oxo-9H-purin-9-ylmethoxy)ethyl Ester Hydrochloride hydrate; Valaciclovir) | Valacyclovir is a prodrug of Acyclovir with inhibitory activity against herpes simplex virus types 1 (HSV-1), 2 (HSV-2), varicella-zoster virus (VZV), Epstein-Barr virus (EBV), and cytomegalovirus (CMV). Valacyclovir is phosphorylated by viral thymidine kinase to acyclovir triphosphate (the active metabolite) which then inhibits herpes viral DNA replication by competitive inhibition of viral DNA polymerase, and by incorporation into and termination of the growing viral DNA chain. Group: Biochemicals. Grades: Highly Purified. CAS No. 124832-27-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Valacyclovir, Hydrochloride. (L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Ester, Hydrochlroride Salt, ValACV) | The L-Valine ester prodrug of Acyclovir. Group: Biochemicals. Alternative Names: L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Ester, Hydrochlroride Salt, ValACV. Grades: Highly Purified. CAS No. 124832-27-5. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| BAY 56-3722 hydrochloride | BAY 56-3722, a water-soluble camptothecin derivative, is a DNA-Intercalating drug that stabilizes the topoisomerase I-DNA covalent complex and forms an enzyme-drug-DNA ternary complex. Synonyms: BAY 56-3722; BAY56-3722; BAY-56-3722; N-[4- (6-Deoxy-3-O-methyl-beta-L-galactopyranosyloxy) phenylaminothiocarbonyl]-L-histidyl-L-valine 4(S)-ethyl-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester hydrochloride; N-[4-(3-O-Methyl-beta-L-fucopyranosyloxy)p; Afeletecan hydrochloride; BAY 38-3441; L-Valine, N- ( ( (4- ( (6-deoxy-3-O-methyl-beta-L-galactopyranosyl) oxy) phenyl) amino) thioxomethyl) -L-histidyl-, (4S)-4-ethyl-3,4,12,14-tetrahydro-3,14-dioxo-1H-pyrano(3',4':6,7)indolizino(1,2-b)quinolin-4-yl ester, hydrochloride (1:1); 215604-75-4 (BAY 56-3722 free base); 215604-74-3 (BAY 56-3722 HCl salt; 215604-66-3 (diastereomeric mixture). Grades: >98%. CAS No. 215604-74-3. Molecular formula: C45H49N7O11S.HCl. Mole weight: 932.447. | |
| Valacyclovir hydrochloride | Valacyclovir hydrochloride (Valaciclovir hydrochloride) is an orally active antiviral agent for herpes simplex, herpes zoster, and herpes B. Valacyclovir hydrochloride inhibits HSV-1 W (50=2.9 μg/ml). Valacyclovir hydrochloride is a proagent of Aciclovir (HY-17422). Uses: Designed for use in research and industrial production. Additional or Alternative Names: VALACICLOVIR HCL;VALACICLOVIR HYDROCHLORIDE;VALACV;VALACYCLOVIR;VALACYCLOVIR HYDROCHLORIDE;L-VALINE 2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9YL)METHOXY]ETHYL ESTER, HYDROCHLORIDE SALT;VALACICLOVIR HCL 99%;VALACICLOVIR HYDROCHLORIDE,98.0+%. Product Category: Inhibitors. CAS No. 124832-27-5. Molecular formula: C13H21ClN6O4. Mole weight: 360.8. Purity: 0.9972. Product ID: ACM124832275. Alfa Chemistry ISO 9001:2015 Certified. |  |
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