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This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH 2 group of donors with NAD + or NADP + as acceptor. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Group: Enzymes. Synonyms: valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Enzyme Commission Number: EC 1.4.1.8. CAS No. 37255-39-3. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Pack: 100ml. Cat No: NATE-1804.
valine dehydrogenase (NAD+)
The enzyme from Streptomyces spp. has no activity with NADP+ [cf. EC 1.4.1.8, valine dehydrogenase (NADP+)]. Group: Enzymes. Enzyme Commission Number: EC 1.4.1.23. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1456; valine dehydrogenase (NAD+); EC 1.4.1.23. Cat No: EXWM-1456.
valine dehydrogenase (NADP+)
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH2 group of donors with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is L-valine:NADP+ oxidoreductase (deaminating). Other names in common use include valine dehydrogenase (nicotinanide adenine dinucleotide phosphate), and valine dehydrogenase (NADP+). Group: Enzymes. Synonyms: valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Enzyme Commission Number: EC 1.4.1.8. CAS No. 37255-39-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1462; valine dehydrogenase (NADP+); EC 1.4.1.8; 37255-39-3; valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Cat No: EXWM-1462.
Valine Ethyl Ester, Hydrochloride
Valine Ethyl Ester, Hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 17609-47-1. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
valine N-monooxygenase
A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-valine, the first committed steps in the biosynthesis of the cyanogenic glucoside linamarin in Manihot esculenta (cassava). The product of the two hydroxylations, N,N-dihydroxy-L-valine, is extremely labile and dehydrates spontaneously. The dehydrated product is then subject to a decarboxylation that produces the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The product, (E)-2-methylpropanal oxime, undergoes a spontaneous isomerization to the (Z) form. The enzyme can also accept L-isoleucine as substrate, with a lower activity. It is different from EC 1.14.13.117 (isoleucine N-monooxygenase), which prefers L-isoleucine. Group: Enzymes. Synonyms: CYP79D1; CYP79D2. Enzyme Commission Number: EC 1.14.13.118. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0718; valine N-monooxygenase; EC 1.14.13.118; CYP79D1; CYP79D2. Cat No: EXWM-0718.
valine-pyruvate transaminase
Different from EC 2.6.1.42, branched-chain-amino-acid-transaminase. Group: Enzymes. Synonyms: transaminase C; valine-pyruvate aminotransferase; alanine-oxoisovalerate aminotransferase. Enzyme Commission Number: EC 2.6.1.66. CAS No. 73379-50-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2907; valine-pyruvate transaminase; EC 2.6.1.66; 73379-50-7; transaminase C; valine-pyruvate aminotransferase; alanine-oxoisovalerate aminotransferase. Cat No: EXWM-2907.
valine-tRNA ligase
This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in valine, leucine and isoleucine biosynthesis and aminoacyl-trna biosynthesis. Group: Enzymes. Synonyms: valyl-tRNA synthetase; valyl-transfer ribonucleate synthetase; valyl-transfer RNA synthetase; valyl-transfer ribonucleic acid synthetase; valine transfer ribonucleate ligase; valine translase. Enzyme Commission Number: EC 6.1.1.9. CAS No. 9023-47-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5664; valine-tRNA ligase; EC 6.1.1.9; 9023-47-6; valyl-tRNA synthetase; valyl-transfer ribonucleate synthetase; valyl-transfer RNA synthetase; valyl-transfer ribonucleic acid synthetase; valine transfer ribonucleate ligase; valine translase. Cat No: EXWM-5664.
Valinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DL-2-AMINO-3-METHYL-1-BUTANOL;DL-VALINOL;2-AMINO-3-METHYL-1-BUTANOL;DL-2-amino-3-methylbutan-1-ol;valinol;1-Butanol, 2-amino-3-methyl-. Product Category: Heterocyclic Organic Compound. CAS No. 473-75-6. Molecular formula: C5H13NO. Mole weight: 103.16. Density: 0.936 g/mL at 25 °C(lit.). Product ID: ACM473756. Alfa Chemistry ISO 9001:2015 Certified.
Valinomycin
Valinomycin is a hydrophobic cyclodepsipeptide with potent antitumor activity. Valinomycin is a highly selective potassium ionophore and this action leads to a diverse range of profound cell membrane effects. More recently, Valinomycin has found application in biosensors. Group: Biochemicals. Grades: Highly Purified. CAS No. 2001-95-8. Pack Sizes: 100mg. US Biological Life Sciences.
Valinomycin is a potassium-specific ionophore, the valinomycin-K + complex can be incorporated into biological bilayer membranes with the hydrophobic surface of valinomycin, destroys the normal K + gradient across the membrane, and as a result kills the cells, incorporating into liposomes can significantly reduces the cytotoxicity and enhances the targeting effect. Valinomycin exhibits antibiotic , antifungal, antiviral, antitumor and insecticidal efficacy, thus can be used for relevant research [1] [2]. Uses: Scientific research. Group: Peptides. Alternative Names: NSC 122023. CAS No. 2001-95-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N6693.
Valiolamine is an exceptional alkaloid compound, used for studying chronic myeloid leukemia (CML). By virtue of its extraordinary capability to impede tyrosine kinases, Valiolamine demonstrates unparalleled potency in studying leukemic manifestations. Synonyms: D-epi-Inositol, 4-amino-3,4-dideoxy-2-C-(hydroxymethyl)-; 4-Amino-3,4-dideoxy-2-C-(hydroxymethyl)-D-epi-inositol; EB 0155. Grades: ≥95%. CAS No. 83465-22-9. Molecular formula: C7H15NO5. Mole weight: 193.20.
Valiphenal
Valiphenal. Group: Biochemicals. Alternative Names: Valifenalate; Methyl 3- (4-chlorophenyl) -3- ({N-[ (propan-2-yloxy) carbonyl]-L-valyl}amino) propanoate. Grades: Highly Purified. CAS No. 283159-90-0. Pack Sizes: 1g, 2g, 5g. Molecular Formula: C19H27ClN2O5. US Biological Life Sciences.
Worldwide
Valnemulin
Semisynthetic antibiotic; derivative of pleuromutilin. Antibacterial. Group: Biochemicals. Alternative Names: 2- [ [2- [ [ (2R) -2-Amino-3-methyl-1-oxobutyl] amino] -1, 1-dimethylethyl] thio] acetic Acid(3aS, 4R, 5S, 6S, 8R, 9R, 9aR, 10R)-6-Ethenyldecahydro-5-hydroxy-4, 6, 9, 10-tetramethyl-1-oxo-3a, 9-propano-3aH-cyclopentacycloocten-8-yl Ester; Econor. Grades: Highly Purified. CAS No. 101312-92-9. Pack Sizes: 1mg, 10mg. US Biological Life Sciences.
Worldwide
Valnemulin
Valnemulin is a pleuromutilin antibiotic used to treat swine dysentery, ileitis, colitis and pneumonia. Synonyms: Econor; Biotilina. Grades: >99% by HPLC. CAS No. 101312-92-9. Molecular formula: C31H52N2O5S. Mole weight: 564.82.
Valnemulin hydrochloride
The hydrochloride salt form of Valnemulin is a wide-spectrum antibiotic that has been found to have strong antibacterial activity especially against mycoplasma and spirochete, and is commonly used as a veterinary drug. It can prevent and control swine dysentery, ileitis, colitis and other intestinal diseases, as well as swine asthma and other respiratory diseases. Synonyms: Valnemulin HCl; UNII-W1GDP58BNQ; W1GDP58BNQ. Grades: >90%. CAS No. 133868-46-9. Molecular formula: C31H53ClN2O5S. Mole weight: 601.28.
Valnemulin hydrochloride
Valnemulin hydrochloride is an orally effective truncated pleurotin antibiotic that inhibits protein synthesis in bacteria by binding to peptidyl transferase in the 50s ribosome subunit. Valnemulin hydrochloride effectively eliminates Mycobacterium bovis in the lungs in an experimental bovine model of Mycoplasma bovis infection. Valnemulin hydrochloride can reduce the mortality of epidemic rabbit enteropathy and has no adverse effect on the growth performance of rabbits [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 133868-46-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0027.
Valnoctamide
Valnoctamide (Valmethamide), a derivative of valproate, suppresses benzodiazepine-refractory status epilepticus. Valnoctamide (Valmethamide) acts directly on GABA A receptors [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Valmethamide. CAS No. 4171-13-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121877.
Anxiolytic. Group: Biochemicals. Alternative Names: 2-Ethyl-d5-3-methylpentan-amide; 2-Ethyl-d5-3-methylvaleramide; Valmethamide-d5; McN-X-181-d5; Axiquel-d5; Nirvanil-d5. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Valoneic Acid Dilactone
Valoneic Acid Dilactone is a polyphenol natural product. It shows an inhibitory effect on 5α-reductase. It also has selectively inhibited RNase L and shows antibacterial activity. Synonyms: Valoneic acid bilactone. Grades: 90% by HPLC. CAS No. 60202-70-2. Molecular formula: C21H10O13. Mole weight: 470.3.
Valopicitabine dihydrochloride
Valopicitabine (NM283) dihydrochloride is a nucleoside analog and the orally bioavailable proagent of the potent anti-HCV agent 2'-C-methylcytidine (NM107). NM107competitively inhibits NS5B polymerase, causing chain termination [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NM283 dihydrochloride. CAS No. 640725-71-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108060A.
Valorphin
Valorphin is an endogenous hemoglobin β-chain (33-39) fragment. Valorphin has opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM. Synonyms: H-Val-Val-Tyr-Pro-Trp-Thr-Gln-OH. Grades: 95%. CAS No. 144313-54-2. Molecular formula: C44H61N9O11. Mole weight: 892.01.
Valorphin TFA
Valorphin TFA is an endogenous hemoglobin β-chain (33-39) fragment. It has opioid analgesic activity, and binds to rat mu-opioid receptor, with an IC50 of 14 nM. Synonyms: H-Val-Val-Tyr-Pro-Trp-Thr-Gln-OH.TFA; L-valyl-L-valyl-L-tyrosyl-L-prolyl-L-tryptophyl-L-threonyl-L-glutamine trifluoroacetic acid. Grades: ≥95%. Molecular formula: C46H62F3N9O13. Mole weight: 1006.03.
Valproate Sodium Impurity 18
Valproate Sodium Impurity 18. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: diethyl 2-ethyl-2-propylmalonate. CAS No. 6065-62-9. Molecular Formula: C12H22O4. Mole Weight: 230.3. Catalog: APB6065629.
Valproate Sodium Impurity 19
Valproate Sodium Impurity 19. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: diethyl 2-isopropyl-2-propylmalonate. CAS No. 62391-98-4. Molecular Formula: C13H24O4. Mole Weight: 244.33. Catalog: APB62391984.
Valproic acid
Valproic acid is an inhibitor of histone deacetylase (HDAC) inhibitor, which has an anticancer effect. Valproic acid was shown to induce proliferation and enhance self-renewal of hematopoietic stem cells (HSC). Uses: Antimanic agents. Synonyms: VPA; 2-Propylpentanoic Acid. Grades: >98%. CAS No. 99-66-1. Molecular formula: C8H16O2. Mole weight: 144.21.
Valproic acid
Valproic acid (VPA) is an orally active HDAC inhibitor, with IC 50 in the range of 0.5 and 2 mM. Valproic acid inhibits HDAC1 ( IC 50 , 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid is used in the epilepsy, bipolar disorder, metabolic disease, HIV infection and prevention of migraine headaches [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Natural products. Alternative Names: Dipropylacetic Acid. CAS No. 99-66-1. Pack Sizes: 500 mg; 1 g; 5 g; 25 g. Product ID: HY-10585.
Valproic Acid
Antiepileptic; Anticonvulsant that also acts as a mood stabilizer for those with bipolar disorder. Group: Biochemicals. Alternative Names: 2-Propylpentanoic Acid. Grades: Highly Purified. CAS No. 99-66-1. Pack Sizes: 10g. US Biological Life Sciences.
Worldwide
Valproic acid b-D-glucuronide
Valproic acid b-D-glucuronide is a compound used in the research of epilepsy and bipolar disorder. It functions as a metabolic precursor of Valproic acid, a drug commonly prescribed to control seizures and stabilize mood. Synonyms: 1-(2-Propylpentanoate) b-D-glucopyranuronic acid; 1-O-Valproyl-b-D-glucopyranuronic acid; Dipropylacetate glucuronide. CAS No. 60113-83-9. Molecular formula: C14H24O8. Mole weight: 320.34.
Valproic Acid β-D-Glucuronide
A metabolite of Valproic acid. Group: Biochemicals. Alternative Names: 1-(2-Propylpentanoate) β-D-Glucopyranuronic Acid; 1-O-Valproyl- β-D-glucopyranuronic Acid; Dipropylacetate Glucuronide; VPA-G; Valproate Glucuronide; Valproic Acid Glucuronide. Grades: Highly Purified. CAS No. 60113-83-9. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Valproic acid-d4
Valproic acid-d 4 is the deuterium labeled Valproic acid. Valproic acid (VPA; 2-Propylpentanoic Acid) is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches[1][2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: VPA-d4; 2-Propylpentanoic Acid-d4. CAS No. 87745-17-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-10585S.
Valproic Acid-d4
Valproic Acid-d4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 87745-17-3. Molecular Formula: C8H12D4O2. Mole Weight: 148.24. Catalog: APB87745173.
Valproic Acid-d6
Valproic Acid-d6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 87745-18-4. Molecular Formula: C8H10D6O2. Mole Weight: 150.25. Catalog: APB87745184.
Method for Determining Identity: Group: Biochemicals. Alternative Names: 2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid. Grades: Highly Purified. CAS No. 87745-18-4. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Valproic Acid EP Impurity D
Valproic Acid EP Impurity D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 52061-75-3. Molecular Formula: C11H22O2. Mole Weight: 186.3. Catalog: APB52061753.
Valproic Acid EP Impurity E
Valproic Acid EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. CAS No. 626-97-1. Molecular Formula: C5H11NO. Mole Weight: 101.15. Catalog: APB626971.
Valproic Acid EP Impurity F
Valproic Acid EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2430-27-5. Molecular Formula: C8H17NO. Mole Weight: 143.23. Catalog: APB2430275.
Valproic Acid EP Impurity G
Valproic Acid EP Impurity G. Uses: For analytical and research use. Group: Impurity standards. CAS No. 52061-73-1. Molecular Formula: C11H23NO. Mole Weight: 185.31. Catalog: APB52061731.
Valproic Acid EP Impurity K
Valproic Acid EP Impurity K. Uses: For analytical and research use. Group: Impurity standards. CAS No. 5343-52-2. Molecular Formula: C8H16O2. Mole Weight: 144.21. Catalog: APB5343522.
Valproic Acid EP Impurity L
Valproic Acid EP Impurity L. Uses: For analytical and research use. Group: Impurity standards. CAS No. 97-61-0. Molecular Formula: C6H12O2. Mole Weight: 116.16. Catalog: APB97610.
Valproic Acid ethyl ester
Valproic Acid ethyl ester. Uses: For analytical and research use. Group: Impurity standards. CAS No. 17022-31-0. Molecular Formula: C10H20O2. Mole Weight: 172.27. Catalog: APB17022310.
Valproic Acid Impurity 10
Valproic Acid Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 109578-13-4. Molecular Formula: C11H20O3. Mole Weight: 200.28. Catalog: APB109578134.
Valproic Acid Impurity 13
Valproic Acid Impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1713239-17-8. Molecular Formula: C15H28O4. Mole Weight: 272.38. Catalog: APB1713239178.
Valproic Acid Impurity 14
Valproic Acid Impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 21269-49-8. Molecular Formula: C12H18O7. Mole Weight: 274.27. Catalog: APB21269498.
Valproic Acid Impurity 16
Valproic Acid Impurity 16. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1636-27-7. Molecular Formula: C9H16O4. Mole Weight: 188.22. Catalog: APB1636277.
Valproic Acid Impurity 2
Valproic Acid Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 141-82-2. Molecular Formula: C3H4O4. Mole Weight: 104.06. Catalog: APB141822.
Valproic Acid Impurity 20
Valproic Acid Impurity 20. Uses: For analytical and research use. Group: Impurity standards. CAS No. 258264-00-5. Molecular Formula: C11H20O4. Mole Weight: 216.28. Catalog: APB258264005.
Valproic Acid Impurity 3
Valproic Acid Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 105-53-3. Molecular Formula: C7H12O4. Mole Weight: 160.17. Catalog: APB105533.
Valproic Acid Impurity 31
Valproic Acid Impurity 31. Uses: For analytical and research use. Group: Impurity standards. CAS No. 49642-47-9. Molecular Formula: C6H12O2. Mole Weight: 116.16. Catalog: APB49642479.
Valproic Acid Impurity 33
Valproic Acid Impurity 33. Uses: For analytical and research use. Group: Impurity standards. CAS No. 3274-28-0. Molecular Formula: C9H18O2. Mole Weight: 158.24. Catalog: APB3274280.
Valproic Acid Impurity 34
Valproic Acid Impurity 34. Uses: For analytical and research use. Group: Impurity standards. CAS No. 60218-41-9. Molecular Formula: C8H14O2. Mole Weight: 142.2. Catalog: APB60218419.
Valproic Acid Impurity 4
Valproic Acid Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 6065-63-0. Molecular Formula: C13H24O4. Mole Weight: 244.33. Catalog: APB6065630.
Valproic Acid Impurity 5
Valproic Acid Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 4443-26-9. Molecular Formula: C14H15NO4. Mole Weight: 261.28. Catalog: APB4443269.
Valproic Acid Impurity 6
Valproic Acid Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 30379-04-5. Molecular Formula: C9H16O5. Mole Weight: 204.22. Catalog: APB30379045.
Valproic Acid Impurity 7
Valproic Acid Impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 72999-08-7. Molecular Formula: C9H16O5. Mole Weight: 204.22. Catalog: APB72999087.
Valproic Acid Impurity 8
Valproic Acid Impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 3115-28-4. Molecular Formula: C10H20O2. Mole Weight: 172.27. Catalog: APB3115284.
Valproic Acid methyl ester
Valproic Acid methyl ester. Uses: For analytical and research use. Group: Impurity standards. CAS No. 22632-59-3. Molecular Formula: C9H18O2. Mole Weight: 158.24. Catalog: APB22632593.
Valproic Acid propyl ester
Valproic Acid propyl ester. Uses: For analytical and research use. Group: Impurity standards. CAS No. 112229-60-4. Molecular Formula: C11H22O2. Mole Weight: 186.3. Catalog: APB112229604.
Valproic Acid Semisodium Salt
Antiepileptic; Anticonvulsant that also acts as a mood stabilizer for those with bipolar disorder. Group: Biochemicals. Alternative Names: 2-Propyl-pentanoic Acid Sodium Salt; Depakote; Divalproex Sodium; Epival; Sodium Hydrogen Bis(2-propylpentanoate); Sodium Hydrogen Bis(2-propylvalerate); Sodium Hydrogen Divalproate; Valdisoval; Valproate Semisodium. Grades: Highly Purified. CAS No. 76584-70-8. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Valproic acid sodium
Valproic acid (Sodium Valproate) sodium is an orally active HDAC inhibitor, with IC 50 in the range of 0.5 and 2 mM, also inhibits HDAC1 ( IC 50 , 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid sodium activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium is used in the treatment of epilepsy, bipolar disorder, metabolic disease, HIV infection and prevention of migraine headaches [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Natural products. Alternative Names: Sodium Valproate sodium. CAS No. 1069-66-5. Pack Sizes: 500 mg; 1 g; 5 g; 25 g. Product ID: HY-10585A.
Valproic acid (Standard)
Valproic acid (Dipropylacetic Acid) (Standard) is an analytical standard for valproic acid. This product is intended for research and analytical applications. Valproic acid is an orally active HDAC inhibitor ( IC 50 =0.5-2 mM), inhibits the activity of HDAC1 ( IC 50 =400 μM), and induces the degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits the proliferation of small cell lung cancer (SCLC) cells. Valproic acid is used in the study of epilepsy, bipolar disorder, metabolic diseases, HIV infection, and migraine [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dipropylacetic Acid (Standard). CAS No. 99-66-1. Pack Sizes: 100 mg; 250 mg; 500 mg. Product ID: HY-10585R.