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| Product | Description | |
|---|---|---|
| Levamisole-d5 Hydrochloride | Levamisole-[d5] Hydrochloride is the labelled analogue of Levamisole, which is a biological response modifier with anthelmintic activity. Synonyms: Levamisole-d5 Hydrochloride; 1246819-64-6; Levamisole-d5 (hydrochloride); (6S)-6-(2,3,4,5,6-Pentadeuteriophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole; hydrochloride; Levamisole-d5 Hydrochloride (1.0 mg/mL in Methanol); (-)-Levamisole-d5 Hydrochloride; DTXSID10857926; 1ST5587AD5-100M; HY-13666S; (6S)-2,3,5,6-Tetrahydro-6-(phenyl-d5)imidazo[2,1-b]thiazole Hydrochloride; CS-0202360; G17715; Levamisole-d5 hydrochloride Solution in Methanol, 100ug/mL; (6S)-6-(~2~H_5_)Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole--hydrogen chloride (1/1); (6S)-6-[(2,3,4,5,6-?H?)phenyl]-2H,3H,5H,6H-imidazo[2,1-b][1,3]thiazole hydrochloride. Grade: 95% by HPLC; 95% atom D. CAS No. 1246819-64-6. Molecular formula: C11H8D5ClN2S. Mole weight: 245.78. |  |
| Levamisole-d5 Hydrochloride | Labeled Levamisole. Biological response modifier with anthelmintic activity. Anthelmintic (nematodes); immunomodulator. Group: Biochemicals. Alternative Names: (6S)-. Grades: Highly Purified. CAS No. 1246819-64-6. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Levamisole HCL USP | Levamisole HCL USP. |  CA, FL & NJ |
| Levamisole hydrochloride | Levamisole hydrochloride, the hydrochloride salt of a water-soluble imidazothiazole derivative, selectively activates acetylcholine receptor ion channels in nerve and muscle of nematodes (EC50 = 6 μM). It has anthelminthic and immunomodulating activities. Uses: Apis for veterinary. Synonyms: Levamisole HCl; Ergamisol; (S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole hydrochloride. Grade: 98%. CAS No. 16595-80-5. Molecular formula: C11H13ClN2S. Mole weight: 240.75. | |
| Levamisole hydrochloride | Levamisole ((-)-Tetramisole) hydrochloride is an anthelmintic and immunomodulator belonging to a class of synthetic imidazothiazole derivatives. Levamisole hydrochloride has antiviral effects against HSV. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Tetramisole hydrochloride. CAS No. 16595-80-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 g; 10 g. Product ID: HY-13666. |  |
| Levamisole hydrochloride | Levamisole hydrochloride. Alternative Names: (-)-Tetramisole Hydrochloride. CAS No. 16595-80-5. Purity: >99.0%. Product ID: FFC-AR-16595805. Molecular formula: C11H13ClN2S. Mole weight: 240.75. IUPAC Name: (6S)-6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole;hydrochloride. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Levamisole hydrochloride | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C11H12N2S · HCl. CAS No. 16595-80-5. Prepack ID 39539315-25g. Molecular Weight 240.75. See USA prepack pricing. |  |
| Levamisole hydrochloride | 5g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C11H12N2S · HCl. CAS No. 16595-80-5. Prepack ID 39539315-5g. Molecular Weight 240.75. See USA prepack pricing. | |
| Levamisole Hydrochloride | Biological response modifier with anthelmintic activity. Anthelmintic (nematodes); immunomodulator. Group: Biochemicals. Alternative Names: (6S)-. Grades: Highly Purified. CAS No. 16595-80-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Levamisole hydrochloride (Standard) | Levamisole (hydrochloride) (Standard) is the analytical standard of Levamisole (hydrochloride). This product is intended for research and analytical applications. Levamisole ((-)-Tetramisole) hydrochloride is an anthelmintic and immunomodulator belonging to a class of synthetic imidazothiazole derivatives. Levamisole hydrochloride has antiviral effects against HSV. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Tetramisole hydrochloride (Standard). CAS No. 16595-80-5. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-13666R. | |
| Levamlodipine | Levamlodipine ((S)-Amlodipine; Levoamlodipin) is an orally active L-type calcium channel blocker and MMP-9 modulator with high permeability and retention properties. Levamlodipine significantly enhances plaque stability and improves lipid profiles by reducing blood pressure, decreasing systolic blood pressure variability, and inhibiting MMP-9 expression in atherosclerotic plaques. Levamlodipine not only alleviates cardiac and aortic hypertrophy and prevents renal atrophy, but also produces synergistic effects in blood pressure reduction and organ protection when combined with bisoprolol (HY-129029). Levamlodipine exerts no significant inhibitory effect on abdominal aortic intimal hyperplasia. When excessively accumulated in the epidermis, Levamlodipine may induce changes in keratin structure, impair the skin barrier and trigger inflammation; long-term use further exacerbates skin irritation caused by local administration. Levamlodipine can be used in research related to hypertension and atherosclerosis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-Amlodipine; Levoamlodipine. CAS No. 103129-82-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14744. | |
| Levamlodipine besylate | Levamlodipine ((S)-Amlodipine; Levoamlodipin) besylate is an orally active L-type calcium channel blocker and MMP-9 modulator with high permeability and retention properties. Levamlodipine besylate significantly enhances plaque stability and improves lipid profiles by reducing blood pressure, decreasing systolic blood pressure variability, and inhibiting MMP-9 expression in atherosclerotic plaques. Levamlodipine besylate not only alleviates cardiac and aortic hypertrophy and prevents renal atrophy, but also produces synergistic effects in blood pressure reduction and organ protection when combined with bisoprolol (HY-129029). Levamlodipine besylate exerts no significant inhibitory effect on abdominal aortic intimal hyperplasia. When excessively accumulated in the epidermis, Levamlodipine besylate may induce changes in keratin structure, impair the skin barrier and trigger inflammation; long-term use further exacerbates skin irritation caused by local administration. Levamlodipine besylate can be used in research related to hypertension and atherosclerosis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (S)-Amlodipine besylate; Levoamlodipine besylate. CAS No. 150566-71-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14744A. | |
| LEVAN | LEVAN. Synonyms: levan from erwinia herbicola;Levan from Zymomonas mobilis; FRUCTAN; fromzymomonasmobilis; (2R, 3S, 4R, 5R)-5-[[ (2R, 3S, 4R, 5R)-5-[[ (2R, 3S, 4R, 5R)-3, 4-dihydroxy-2, 5-bis (hydroxymethyl)oxolan-2-yl]oxymethyl]-3, 4-dihydroxy-2- (hydroxymethyl)oxolan-2-yl]oxymethyl]-2- (hydroxymethyl)oxolane-2, 3, 4-triol; LEVAN, FROM SERRATIA LEVANICUM;Gum levan. CAS No. 9013-95-0. Product ID: CDF4-0168. Molecular formula: C18H32O16. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; LEVAN; CDF4-0168; 9013-95-0; C18H32O16; 1308068-626-2; 9013-95-0. Purity: 0.99. EC Number: 1308068-626-2. Solubility: H2O: 10 mg/mL, hazy, faintly yellow. Storage: 2-8°C. Product Description: Levan is a polysaccharide produced by some microorganisms and plants. It is a non-typical biopolymer composed of fructose units linked by β-(2→6). Levan is an exopolysaccharide (synthesized outside the cell). |  |
| levanase | Levanase (EC 3.2.1.65) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. Group: Enzymes. Synonyms: levan hydrolase; 2,6-β-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Levanase. 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-3929; levanase; EC 3.2.1.65; 9041-11-6; levan hydrolase; 2,6-β-D-fructan fructanohydrolase. Cat No: EXWM-3929. |  |
| Levanase | Levanase is a slime-dissolving enzyme of Rhodotorula species. Levanase performs random hydrolysis of β-2,6 fructofuranosyl linkages in β-2,6 fructans containing more than 3 fructose units[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9041-11-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-E70011. | |
| Levanase 32A from Bacillus subtilis, Recombinant | Levanase (EC 3.2.1.65, levan hydrolase, 2,6-beta-D-fructan fructanohydrolase) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. This enzyme catalyses the following chemical reaction: Random hydrolysis of (2->6)-beta-D-fructofuranosidic linkages in (2->6)-beta-D-fructans (levans) containing more than 3 fructose units. Group: Enzymes. Synonyms: Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Purity: >90% by SDS-PAGE. Levanase. Mole weight: 37.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase; Levanase 32A. Cat No: NATE-1386. | |
| Levanase 32A from Bacteroides thetaiotaomicron, Recombinant | Levanase (EC 3.2.1.65, levan hydrolase, 2,6-beta-D-fructan fructanohydrolase) is an enzyme with systematic name (2->6)-beta-D-fructan fructanohydrolase. This enzyme catalyses the following chemical reaction: Random hydrolysis of (2->6)-beta-D-fructofuranosidic linkages in (2->6)-beta-D-fructans (levans) containing more than 3 fructose units. Group: Enzymes. Synonyms: Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase. Enzyme Commission Number: EC 3.2.1.65. CAS No. 9041-11-6. Purity: >90% by SDS-PAGE. Levanase. Mole weight: 37.9 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Levanase; EC 3.2.1.65; levan hydrolase; 2,6-beta-D-fructan fructanohydrolase; (2->6)-beta-D-fructan fructanohydrolase; Levanase 32A. Cat No: NATE-1385. | |
| Levan from Erwinia herbicola | Levan from Erwinia herbicola. CAS No. 9013-95-0. Molecular formula: C18H32O16. Mole weight: 504.4g/mol. IUPAC Name: (2R,3S,4S,5R)-5-[[(2R,3S,4S,5R)-5-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-2-(hydroxymethyl)oxolan-2-yl]oxymethyl]-2-(hydroxymethyl)oxolane-2,3,4-triol. SMILES: C(C1C(C(C(O1)(CO)OCC2C(C(C(O2)(CO)OCC3C(C(C(O3)(CO)O)O)O)O)O)O)O)O. InChI: InChI=1S/C18H32O16/c19-1-7-10(23)14(27)17(5-21,33-7)31-3-9-12(25)15(28)18(6-22,34-9)30-2-8-11(24)13(26)16(29,4-20)32-8/h7-15,19-29H,1-6H2/t7-,8-,9-,10-,11-,12-,13+,14+,15+,16-,17-,18-/m1/s1. |  |
| levan fructotransferase (DFA-IV-forming) | This enzyme, like EC 4.2.2.17 [inulin fructotransferase (DFA-I-forming)] and EC 4.2.2.18 [inulin fructotransferase (DFA-III-forming)] eliminates the fructan chain from the terminal disaccharide leaving a difructose dianhydride. These enzymes have long been known as fructotransferases, so this is retained in the accepted name. Since the transfer is intramolecular, the reaction is an elimination and, hence, the enzyme is a lyase, belonging in EC 4. Group: Enzymes. Synonyms: 2,6-β-D-fructan D-fructosyl-D-fructosyltransferase (forming di-β-D-fructofuranose 2,6':2',6-dianhydride); levan fructotransferase; 2,6-β-D-fructan lyase (di-β-D-fructofuranose-2,6':2',6-dianhydride-forming). Enzyme Commission Number: EC 4.2.2.16. CAS No. 88593-15-1. 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-5091; levan fructotransferase (DFA-IV-forming); EC 4.2.2.16; 88593-15-1; 2,6-β-D-fructan D-fructosyl-D-fructosyltransferase (forming di-β-D-fructofuranose 2,6':2',6-dianhydride); levan fructotransferase; 2,6-β-D-fructan lyase (di-β-D-fructofuranose-2,6':2',6-dianhydride-forming). Cat No: EXWM-5091. | |
| levansucrase | Some other sugars can act as D-fructosyl acceptors. Group: Enzymes. Synonyms: sucrose 6-fructosyltransferase; β-2,6-fructosyltransferase; β-2,6-fructan:D-glucose 1-fructosyltransferase; sucrose:2,6-β-D-fructan 6-β-D-fructosyltransferase; sucrose:(2?6)-β-D-fructan 6-β-D-fructosyltransferase. Enzyme Commission Number: EC 2.4.1.10. CAS No. 9030-17-5. Levansucrase. 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-2327; levansucrase; EC 2.4.1.10; 9030-17-5; sucrose 6-fructosyltransferase; β-2,6-fructosyltransferase; β-2,6-fructan:D-glucose 1-fructosyltransferase; sucrose:2,6-β-D-fructan 6-β-D-fructosyltransferase; sucrose:(2?6)-β-D-fructan 6-β-D-fructosyltransferase. Cat No: EXWM-2327. | |
| Levcromakalim | Levcromakalim ((-)-Cromakalim) is an ATP-sensitive K+ channel (KATP) activator. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (-)-Cromakalim; BRL 38227. CAS No. 94535-50-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-14255. | |
| L-evernosamine nitrososynthase | Requires FAD. Isolated from the bacterium Micromonospora carbonacea var. africana. The nitroso group is probably spontaneously oxidized to a nitro group giving dTDP-β-L-evernitrose, which is involved in the biosynthesis of the antibiotic everninomycin. The reaction was studied using dTDP-β-L-4-epi-vancosamine (dTDP-4-O-desmethyl-β-L-evernitrosamine). Group: Enzymes. Enzyme Commission Number: EC 1.14.13.187. 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-0786; L-evernosamine nitrososynthase; EC 1.14.13.187. Cat No: EXWM-0786. | |
| Levetiracetam | Levetiracetam, an antiepileptic agent, binds the synaptic vesicle protein SV2A. Levetiracetam enhances Temozolomide effect on glioblastoma stem cell proliferation and apoptosis. Levetiracetam modulates HDAC levels ultimately silencing MGMT, thus increasing Temozolomide effectiveness. A chemosensitizer agent[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UCB L059. CAS No. 102767-28-2. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-B0106. | |
| Levetiracetam | Levetiracetam is a compound which inhibits burst firing without affecting normal neuronal excitability. Category: Active pharmaceutical ingredients. CAS No. 102767-28-2. Product ID: API102767282. Molecular formula: C8H14N2O2. Mole weight: 170.21. Appearance: Crystalline. |  |
| Levetiracetam | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C8H14N2O2. CAS No. 102767-28-2. Prepack ID 89966312-25g. Molecular Weight 170.21. See USA prepack pricing. | |
| Levetiracetam-[2,3,3,4,4,4-butyramide-d6] | Levetiracetam-[d3] is an isotope labelled analog of Levetiracetam. Levetiracetam is a medication used to treat epilepsy. Synonyms: (αS)-α-(Ethyl-1,1,2,2,2-d5)-2-oxo-1-pyrrolidineacetamide-α-d; (-)-Levetiracetam-d6. Grade: 98% by CP; 98% atom D. CAS No. 1133229-29-4. Molecular formula: C8H8D6N2O2. Mole weight: 176.25. | |
| Levetiracetam acid | Levetiracetam acid. Alternative Names: LEVETIRACETAM ACID;(R)-alpha-Ethyl-2-oxo-1-pyrrolidineacetic acid;Levetiracetam Carboxylic Acid;(.alpha.R)-.alpha.-ethyl-2-oxo-1-Pyrrolidineacetic acid. CAS No. 103833-72-3. Purity: 96%. Product ID: ACM103833723. Molecular formula: C8H13NO3. Mole weight: 171.19. IUPAC Name: (2R)-2-(2-oxopyrrolidin-1-yl)butanoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Levetiracetam Carboxylic Acid | Levetiracetam intermediate. Group: Biochemicals. Alternative Names: (αS)-. Grades: Highly Purified. CAS No. 102849-49-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Levetiracetam-d3 | Labeled Levetiracetam, which is used as an anticonvulsant. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Levetiracetam-d3 (contains d0) | The labelled (S)-enantiomer of Etiracetam (E932970) and the ethyl analog of Piracetam (P500800). Used as an anticonvulsant. Group: Biochemicals. Alternative Names: (αS)-α-(Ethyl-d3)-2-oxo-. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Levetiracetam EP Impurity A | Levetiracetam EP Impurity A. Uses: For analytical and research use. CAS No. 67118-31-4. Molecular formula: C8H13NO3. Mole weight: 171.2. Catalog: APB67118314. |  |
| Levetiracetam EP Impurity B | Levetiracetam EP Impurity B. Uses: For analytical and research use. CAS No. 358629-47-7. Molecular formula: C8H12N2O2. Mole weight: 168.2. Catalog: APB358629477. | |
| Levetiracetam EP Impurity C | Levetiracetam EP Impurity C. Uses: For analytical and research use. CAS No. 72762-00-6. Molecular formula: C5H5NO. Mole weight: 95.1. Catalog: APB72762006. | |
| Levetiracetam EP Impurity C | Levetiracetam EP Impurity C. Uses: For analytical and research use. Alternative Names: pyridin-2-ol. CAS No. 142-08-5. Molecular formula: C5H5NO. Mole weight: 95.1. Catalog: APB142085. | |
| Levetiracetam EP Impurity D | Levetiracetam EP Impurity D. Uses: For analytical and research use. CAS No. 103765-01-1. Molecular formula: C8H14N2O2. Mole weight: 170.21. Catalog: APB103765011. | |
| Levetiracetam EP Impurity G | An impurity of Levetiracetam, a medication indicated for the treatment of epilepsy. Synonyms: L-α-Aminobutyramide; H-Abu(2)-NH2; H-Abu(α)-NH2; (S)-2-Aminobutanamide. CAS No. 7324-11-0. Molecular formula: C4H10N2O. Mole weight: 102.14. | |
| Levetiracetam EP Impurity G | Levetiracetam EP Impurity G. Uses: For analytical and research use. CAS No. 7324-11-0. Molecular formula: C4H10N2O. Mole weight: 102.14. Catalog: APB7324110. | |
| Levetiracetam impurity 1 | Levetiracetam impurity 1 is an impurity of Levetiracetam (HY-B0106). Uses: Scientific research. Category: Signaling pathways. CAS No. 102849-49-0. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-135321. | |
| Levetiracetam Impurity 12 | Levetiracetam Impurity 12. Uses: For analytical and research use. CAS No. 10476-43-0. Molecular formula: C4H11ClN2O. Mole weight: 138.6. Catalog: APB10476430. | |
| Levetiracetam Impurity 13 | Levetiracetam Impurity 13. Uses: For analytical and research use. CAS No. 102767-31-7. Molecular formula: C8H15ClN2O2. Mole weight: 206.67. Catalog: APB102767317. | |
| Levetiracetam Impurity 17 | Levetiracetam Impurity 17. Uses: For analytical and research use. CAS No. 93554-80-4. Molecular formula: C4H9ClN2. Mole weight: 120.58. Catalog: APB93554804. | |
| Levetiracetam Impurity 27 (Hydrochloride) | Levetiracetam Impurity 27 (Hydrochloride). Uses: For analytical and research use. Alternative Names: (S)-2-amino-N-((S)-1-amino-1-oxobutan-2-yl)butanamide hydrochloride. Molecular formula: C8H17N3O2·HCl. Mole weight: 223.7. Catalog: APB01616. | |
| Levetiracetam Impurity H | Levetiracetam Impurity H. Uses: For analytical and research use. Alternative Names: (S)-2-aminobutanoic acid. CAS No. 1492-24-6. Molecular formula: C4H9NO2. Mole weight: 103.12. Catalog: APB1492246. | |
| Levetiracetam Impurity K | Levetiracetam Impurity K. Uses: For analytical and research use. Alternative Names: 4-chlorobutanoic acid. CAS No. 627-00-9. Molecular formula: C4H7ClO2. Mole weight: 122.55. Catalog: APB627009. | |
| Levetiracetam Related Compound A | Levetiracetam Related Compound A. Uses: For analytical and research use. CAS No. 102767-31-7. Mole weight: 206.67. Catalog: AP102767317. | |
| Levetiracetam Related Compound B | An impurity of Levetiracetam, a medication indicated for the treatment of epilepsy. Synonyms: L-2-Aminobutanamide HCl; S-2-Aminobutanamide HCl; (S)-2-Aminobutanamide Monohydrochloride. Grade: ≥ 98% (HPLC). CAS No. 7682-20-4. Molecular formula: C4H11ClN2O. Mole weight: 138.6. | |
| Levetiracetam Related Compound B | Levetiracetam Related Compound B. Uses: For analytical and research use. CAS No. 7682-20-4. Mole weight: 138.60. Catalog: AP7682204. | |
| Levetiracetam-[ring-d6] | Levetiracetam-[ring-d6] is an isotope labelled analog of Levetiracetam. Levetiracetam is a medication used to treat epilepsy. Synonyms: (2S)-2-[2-Oxo(2H6)pyrrolidin-1-yl]butanamide. Grade: 98% by CP; 98% atom D. CAS No. 1133229-30-7. Molecular formula: C8H8D6N2O2. Mole weight: 176.25. | |
| Levetiracetam (UCB-L059, SIB-S1, Keppra) | Used as an anticonvulsant. Group: Biochemicals. Alternative Names: UCB-L059; SIB-S1; Keppra; (αS)-α-Ethyl-2-oxo-1-pyrrolidineacetamide; 2(S)-(2-Oxopyrrolidin-1-yl)butyramide; (-)-Levetiracetam; Levesam 500; (S)-Levetiracetam. Grades: Highly Purified. CAS No. 102767-28-2. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C?H??N?O?, Molecular Weight: 170.21. US Biological Life Sciences. | Worldwide |
| Levetiracetam USP Related Compound B | Levetiracetam USP Related Compound B. Uses: For analytical and research use. Alternative Names: (S)-2-aminobutanamide hydrochloride. CAS No. 7682-20-4. Molecular formula: C4H11ClN2O. Mole weight: 138.6. Catalog: APB7682204. | |
| Levine Eosin-Methylene Blue Agar Medium | Levine Eosin-Methylene Blue Agar Medium. Uses: For analytical and research use. Alternative Names: Levine EMB Agar. Catalog: APB12482. | |
| Levisticum officinale oil | Levisticum officinale oil. Alternative Names: Lovageroofoil. CAS No. 8016-31-7. Purity: 0.98. Product ID: CI-EO-0086. Molecular formula: C222H230N14O23S2. Mole weight: 3526 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Levistilide A | Levistilide A. Group: Biochemicals. Grades: Plant Grade. CAS No. 88182-33-6. Pack Sizes: 20mg. Molecular Formula: C24H28O4, Molecular Weight: 380.48. US Biological Life Sciences. | Worldwide |
| Levistolide A | Levistolide A. Group: Biochemicals. CAS No. 88182-33-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Levobunolol hydrochloride | Levobunolol (l-Bunolol) hydrochloride is a non-selective β-adrenergic antagonist and vasodilator. By blocking calcium ion influx and reducing the sensitivity of vascular smooth muscle to calcium, Levobunolol hydrochloride effectively dilates the ciliary arteries and increases ocular blood flow, so it is widely used in research on glaucoma and ocular hypertension. Levobunolol hydrochloride inhibits the β-receptor signaling pathway and the expression of related proliferation markers (such as CK3, CK14, CK19, Ki67) in corneal cells. In rabbit models, Levobunolol hydrochloride not only does not inhibit corneal epithelial regeneration, but also accelerates the healing of mechanical injury without adverse effects. Levobunolol hydrochloride also inhibits histamine-induced vasoconstriction and intracellular calcium elevation, exhibiting unique vascular regulatory activity. Levobunolol hydrochloride protects ocular blood flow and promotes corneal repair[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: l-Bunolol hydrochloride. CAS No. 27912-14-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1035. | |
| Levobupivacaine HCL | S-enantiomer of bupivacaine that is used as a local anesthetic and for regional nerve blocks, including EPIDURAL ANESTHESIA. Category: Anesthetic analgesia apis. Synonyms: Levobupivacaine hydrochloride. Chirocaine. Bupicaine hydrochloride (-). CAS No. 27262-48-2. Product ID: API27262482. Molecular formula: C18H29ClN2O. Mole weight: 324.9. EINECS: 642-955-1. SMILES: CCCCN1CCCCC1C(=O)NC2=C(C=CC=C2C)C.Cl. Standard: In-House. | |
| Levocabastine hydrochloride | Levocabastine (R 50547) hydrochloride is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a Ki of 17 nM for mNTR2. Levocabastine hydrochloride can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: R 50547 hydrochloride. CAS No. 79547-78-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-14277A. | |
| Levocabastine hydrochloride | Levocabastine HCl is an agent with antihistaminic activity. Category: Active pharmaceutical ingredients. CAS No. 79547-78-7. Product ID: API79547787. Molecular formula: C26H30ClFN2O2. Mole weight: 456.98. | |
| Levocabastine Impurity 1 | Levocabastine Impurity 1. Uses: For analytical and research use. Molecular formula: C26H30FNO4. Mole weight: 439.53. Catalog: APB12103. | |
| Levocabastine Impurity 10 | Levocabastine Impurity 10. Uses: For analytical and research use. CAS No. 179064-61-0. Molecular formula: C13H12FNO. Mole weight: 217.24. Catalog: APB179064610. | |
| Levocabastine Impurity 11 | Levocabastine Impurity 11. Uses: For analytical and research use. CAS No. 577036-07-8. Molecular formula: C13H12FNO. Mole weight: 217.24. Catalog: APB577036078. | |
| Levocabastine Impurity 12 | Levocabastine Impurity 12. Uses: For analytical and research use. CAS No. 56326-98-8. Molecular formula: C13H12FNO. Mole weight: 217.24. Catalog: APB56326988. | |
| Levocabastine Impurity 13 | Levocabastine Impurity 13. Uses: For analytical and research use. CAS No. 80139-90-8. Molecular formula: C25H27FN2O2. Mole weight: 406.5. Catalog: APB80139908. | |
| Levocabastine Impurity 14 | Levocabastine Impurity 14. Uses: For analytical and research use. CAS No. 105452-51-5. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB105452515. | |
| Levocabastine Impurity 15 | Levocabastine Impurity 15. Uses: For analytical and research use. CAS No. 105452-52-6. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB105452526. | |
| Levocabastine Impurity 16 | Levocabastine Impurity 16. Uses: For analytical and research use. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB12116. | |
| Levocabastine Impurity 17 | Levocabastine Impurity 17. Uses: For analytical and research use. Molecular formula: C26H29FN2O2. Mole weight: 420.53. Catalog: APB12117. | |
| Levocabastine Impurity 18 | Levocabastine Impurity 18. Uses: For analytical and research use. Molecular formula: C26H31FN2O3. Mole weight: 438.54. Catalog: APB12118. | |
| Levocabastine Impurity 19 | Levocabastine Impurity 19. Uses: For analytical and research use. Molecular formula: C25H24BrFN2. Mole weight: 451.38. Catalog: APB12119. | |
| Levocabastine Impurity 2 | Levocabastine Impurity 2. Uses: For analytical and research use. Molecular formula: C26H31FN2O4. Mole weight: 454.55. Catalog: APB12104. | |
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