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| Product | Description | |
|---|---|---|
| Lichenase 16A from Clostridium thermocellum, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Syn. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 26.7 kDa. Activity: 9000 U/mg. 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: Clostridium thermocellum. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 16A. Cat No: NATE-1422. |  |
| Lichenase 16A from Paenibacillus polymyxa, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Synonyms: endo-1,3-β-D-. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 26.2 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: Paenibacillus polymyxa. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 16A. Cat No: NATE-1421. | |
| Lichenase 16A from Ruminococcus flavefaciens, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Synonyms: endo-1,3-&be. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 89.2 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: Ruminococcus flavefaciens. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 16A. Cat No: NATE-1423. | |
| Lichenase 16D from Ruminococcus flavefaciens, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Synonyms: endo-1,3-&be. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 30.5 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: Ruminococcus flavefaciens. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 16D. Cat No: NATE-1424. | |
| Lichenase 26A & Cellulase 5E from Clostridium thermocellum, Recombinant | Cellulase is any of several enzymes produced chiefly by fungi, bacteria, and protozoans that catalyze cellulolysis, the decomposition of cellulose and of some related polysaccharides; specifically, the hydrolysis of the 1,4-beta-D-glycosidic linkages in cellulose, hemicellulose, lichenin, and cereal beta-D-glucans. Cellulases break down the cellulose molecule into monosaccharides ("simple sugars") such as beta-glucose, or shorter polysaccharides and oligosaccharides. The name is also used for any naturally occurring mixture or complex of various such enzymes, that act serially or synergistically to decompose cellulosic material. Group: Enzymes. Synonyms: C...um thermocellum. Cellulase, thermostable; 1,4-(1,3:1,4)-β-D-Glucan 4-glucano-hydrolase; EC 3.2.1.4; Cellulase; endo-1,4-β-D-glucanase; β-1,4-glucanase; β-1,4-endoglucan hydrolase; celluase A; cellulosin AP; endoglucanase D; alkali cellulase; cellulase A 3; celludextrinase; 9.5 cellulase; avicelase; pancellase SS; Cellulase 5E; endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase I | |
| Lichenase 26A from Clostridium thermocellum, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Syno. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 32.5 kDa. Activity: 700 U/mg. 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: Clostridium thermocellum. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 26A. Cat No: NATE-1426. | |
| Lichenase 5A from Thermotoga maritima, Recombinant | β-glucanases degrade β-1,4-glucans of cellulose, xyloglucan and β-1,4-xylan. β-Glucanase represents a group of carbohydrate enzymes which break down glycosidic bonds within beta-glucan. It forms the main constituent of fungal cell walls and could be a potential structural and storage polysaccharide of marine macro-algae. It has the ability to degrade fungal cell walls and may be involved in defense mechanism of plants against pathogenic fungi. Group: Enzymes. Synonyms: endo-1,3-β-D-glucanas. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 41.3 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: Thermotoga maritima. endo-1,3-β-D-glucanase; laminarinase; laminaranase; β-1,3-glucanase; β-1,3-1,4-glucanase; endo-1,3-β-glucanase; endo-β-1,3 (4)-glucanase; endo-β-1,3-1,4-glucanase; endo-β-(1?3)-D-glucanase; endo-1,3-1,4-β-D-glucanase; endo-β-(1-3)-D-glucanase; endo-β-1,3-glucanase IV; endo-1,3-β-D-glucanase; 1,3-(1,3; 1,4)-β-D-glucan 3 (4)-glucanohydrolase; EC 3.2.1.73; Lichenase 5A. Cat No: NATE-1425. | |
| Lichenase, Microorganism | Lichenase, Microorganism (endo-1,3:1,4-β-D-Glucanase) is a specific, endo-(1-3),(1-4)-β-D-glucan 4-glucanohydrolase. Lichenase, Microorganism solubilizes β-glucans from cereal grains and gives gluco-oligosaccharides (GOS). Lichenase, Microorganism can be used in the degradation of polysaccharides in the cell walls [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: endo-1,3:1,4-β-D-Glucanase. CAS No. 37288-51-0. Pack Sizes: 5 KU; 10 KU; 50 KU. Product ID: HY-E70013. |  |
| Lichenicidin | Lichenicidin is an antibacterial peptide isolated from Bacillus licheniformis (strain VK21/DSM 13). Synonyms: Lantibiotic lichenicidin VK21 A1; Thr-Ile-Thr-Leu-Ser-Thr-Cys-Ala-Ile-Leu-Ser-Lys-Pro-Leu-Gly-Asn-Asn-Gly-Tyr-Leu-Cys-Thr-Val-Thr-Lys-Glu-Cys-Met-Pro-Ser-Cys-Asn. |  |
| Lichenin | Lichenin is an antibacterial peptide isolated from Bacillus licheniformis. Synonyms: Ile-Ser-Leu-Glu-Ile-Cys-Ala-Ile-Phe-His-Asp-Asn. Molecular formula: C6H10O5. Mole weight: 162.14. | |
| licheninase | Acts on lichenin and cereal β-D-glucans, but not on β-D-glucans containing only 1,3- or 1,4-bonds. Group: Enzymes. Synonyms: lichenase; β-(1?4)-D-glucan 4-glucanohydrolase; 1,3;1,4-β-glucan endohydrolase; 1,3;1,4-β-glucan 4-glucanohydrolase; 1,3-1,4-β-D-glucan 4-glucanohydrolase. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. β-glucanase. 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-3937; licheninase; EC 3.2.1.73; 37288-51-0; lichenase; β-(1?4)-D-glucan 4-glucanohydrolase; 1,3;1,4-β-glucan endohydrolase; 1,3;1,4-β-glucan 4-glucanohydrolase; 1,3-1,4-β-D-glucan 4-glucanohydrolase. Cat No: EXWM-3937. | |
| Lichen (trace elements) | certified Reference Material. Group: Certified reference materials (crms). |  |
| Lichenysin G | It is produced by the strain of Bacillus licheniformis IM 1307. It acts as a surfactant and is 10 times more active than Surfactin. Molecular formula: C42H72N8O12. Mole weight: 881.06. | |
| Lichexanthone | Lichexanthone is separated from the bark of Cupania cinerea. It has a role as a plant metabolite. CAS No. 15222-53-4. Molecular formula: C16H14O5. Mole weight: 286.28. | |
| LICHROLUT EN, 40-120 MYM | LICHROLUT EN, 40-120 MYM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LICHROLUT EN, 40-120 MYM;LICHROLUT(R) EN. Product Category: Heterocyclic Organic Compound. CAS No. 165039-45-2. Purity: 0.96. Product ID: ACM165039452. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Licoagrochalcone a | Licoagrochalcone a. Uses: Designed for use in research and industrial production. Additional or Alternative Names: licoagrochalcone A, CHEMBL229885, LICOAGROCHALCONEA, SCHEMBL632907, DNC007424, LMPK12120068, 3-Prenyl-4,2,4-trihydroxychalcone, 202815-28-9. Product Category: Heterocyclic Organic Compound. CAS No. 202815-28-9. Molecular formula: C20H20O4. Mole weight: 324.370400 [g/mol]. Purity: 0.96. IUPACName: (E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one. Canonical SMILES: CC(=CCC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O)C. Product ID: ACM202815289. Alfa Chemistry ISO 9001:2015 Certified. | |
| Licochalcone A | Licochalcone A is a chalconoid, a type of natural phenols. It can be isolated from root of Glycyrrhiza glabra (liquorice) or Glycyrrhiza inflata. It is a potent membrane-active agent that transforms normal erythrocytes into echinocytes. It exhibits potent antimalarial activity and might be developed into a new antimalarial drug. It had anti-tumor activity in all cell lines tested and enhanced the effect of paclitaxel and vinblastine chemotherapy. Synonyms: 4,4'-Dihydroxy-3-α,α-dimethylallyl-6-methoxychalcone; 7-Dimethoxycoumarin; 3-Dimethylallyl-4,4'-dihydroxy-6-methoxychalcone; (E)-3-[5-(1,1-Dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-2-propen-1-one; (2E)-3-[5-(1,1-Dimethyl-2-propen-1-yl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-2-propen-1-one; 2-Propen-1-one, 3-[5-(1,1-dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-, (2E)-; 2-Propen-1-one, 3-[5-(1,1-dimethyl-2-propenyl)-4-hydroxy-2-methoxyphenyl]-1-(4-hydroxyphenyl)-, (E)-. Grade: >98%. CAS No. 58749-22-7. Molecular formula: C21H22O4. Mole weight: 338.40. | |
| Licochalcone A | Licochalcone A (LCA), a flavonoid isolated, presents obvious anti-cancer effects, displays broad-spectrum inhibition against UDP-glucuronosyltransferases (UGTs) [1]. Licochalcone A (LCA) exhibits strong inhibitory effects against UGT1A1, 1A3, 1A4, 1A6, 1A7, 1A9, and 2B7 (both IC 50 and K i values lower than 5 μM) [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Licochalcone-A. CAS No. 58749-22-7. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0372. | |
| Licochalcone A | Licochalcone A. Group: Biochemicals. Grades: Plant Grade. CAS No. 58749-22-7. Pack Sizes: 20mg. Molecular Formula: C21H22O4, Molecular Weight: 338.4. US Biological Life Sciences. |  Worldwide |
| Licochalcone B | Licochalcone B. Group: Biochemicals. CAS No. 58749-23-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Licochalcone B | Licochalcone B is extracted from the roots of Glycyrrhiza glabra L. It inhibits the adhesion,invasion and metastasis of human malignant bladder cancer T24 cells. It could significantly reduce the LPS-induced production of NO, TNFalpha and MCP-1. Synonyms: (2E)-3-(3,4-Dihydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)-2-propen-1-one; 2-Propen-1-one, 3-(3,4-dihydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)-, (E)-; (E)-3-(3,4-Dihydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)-2-propen-1-one; 3,4,4'-Trihydroxy-2-methoxy-trans-chalcone; 3,4,4'-Trihydroxy-2-Methoxychalcone. Grade: >98%. CAS No. 58749-23-8. Molecular formula: C16H14O5. Mole weight: 286.28. | |
| Licochalcone B | Licochalcone B is an extract from the root of Glycyrrhiza uralensis. Licochalcone B inhibits amyloid ? (42) self-aggregation (IC50=2.16 ?M) and disaggregate pre-formed A?42 fibrils, reduce metal-induced A?42 aggregation through chelating metal ionsLicochalcone B inhibits phosphorylation of NF-?B p65 in LPS signaling pathway. Licochalcone B inhibits growth and induces apoptosis of NSCLC cells. Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7?NLRP3 interaction[1][2][3][4]. Uses: Scientific research. Group: Natural products. CAS No. 58749-23-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0373. | |
| Licochalcone C | Licochalcone C could inhibit α-glucosidase , with IC 50 s of <100 nM and 92.43 μM for α-glucosidase and protein tyrosine phosphatase 1B (PTP1B), respectively. Uses: Scientific research. Group: Natural products. CAS No. 144506-14-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0374. | |
| Licochalcone D | Licochalcone D, a flavonoid compound mainly existing in the root of Glycyrrhiza uralensis, is a potent and orally active inhibitor of NF-kappaB (NF-?B) p65. Licochalcone D possesses antioxidant, anti-inflammatory, anti-cancer properties[1][2]. Uses: Scientific research. Group: Natural products. CAS No. 144506-15-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N4187. | |
| Licochalcone E | Licochalcone E, a flavonoid compound isolated from Glycyrrhiza uralensis, inhibits NF-?B and AP-1 transcriptional activity through the inhibition of AKT and MAPK activation[1]. Uses: Scientific research. Group: Natural products. CAS No. 864232-34-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N4182. | |
| licodione 2'-O-methyltransferase | As well as licodione [1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1,3-propanedione], the 2''-hydroxy-derivative and isoliquiritigenin can act as acceptors, but more slowly. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.65. CAS No. 77000-07-8. 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-1967; licodione 2'-O-methyltransferase; EC 2.1.1.65; 77000-07-8. Cat No: EXWM-1967. | |
| licodione synthase | A heme-thiolate protein (P-450). It probably forms 2-hydroxyliquiritigenin which spontaneously forms licodione. NADH can act instead of NADPH, but more slowly. Group: Enzymes. Enzyme Commission Number: EC 1.14.13.87. CAS No. 157972-05-9. 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-0895; licodione synthase; EC 1.14.13.87; 157972-05-9. Cat No: EXWM-0895. | |
| Licofelone | Licofelone (ML-3000) is a dual COX/5-lipoxygenase (5-LOX) inhibitor ( IC 50 =0.21/0.18 μM, respectively) for the treatment of osteoarthritis. Licofelone exerts anti-inflammatory and anti-proliferative effects. Licofelone induces apoptosis , and decreases the production of proinflammatory leukotrienes and prostaglandins [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ML-3000. CAS No. 156897-06-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1452. | |
| Licofelone | Dual inhibitor of cyclooxygenase and 5-lipoxygenase. Anti-inflammatory. Group: Biochemicals. Alternative Names: 6-(4-Chlorophenyl)-2,3-dihydro-2,2-dimethyl-7-phenyl-1H-pyrrolizine-5-acetic Acid; ML-3000. Grades: Highly Purified. CAS No. 156897-06-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg. Molecular Formula: C??H??ClNO?, Molecular Weight: 379.88. US Biological Life Sciences. | Worldwide |
| Licoflavone B | Licoflavone B is a flavonoid isolated from Glycyrrhiza inflata, inhibits S. mansoni ATPase (IC50, 23.78 μM) and ADPase (IC50, 31.50 μM) activity. Anti-schistosomiasis activity. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 91433-17-9. Molecular formula: C25H26O4. Mole weight: 390.47. Purity: 0.9991. Canonical SMILES: O=C1C=C(C2=CC=C(O)C(C/C=C(C)\C)=C2)OC3=CC(O)=C(C/C=C(C)\C)C=C13. Product ID: ACM91433179. Alfa Chemistry ISO 9001:2015 Certified. | |
| Licogliflozin | Licogliflozin is a sodium glucose cotransporter ( SGLT1 and SGLT2 ) inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LIK066. CAS No. 1291094-73-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109092. | |
| Licoisoflavone A | Licoisoflavone A. Group: Biochemicals. CAS No. 66056-19-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Licoisoflavone A | Licoisoflavone A, a potential MRP inhibitor, is a natural flavonoid derived from the roots of Glycyrrhiza uralensis Fisch. It inhibits lipid peroxidation with an IC50 of 7.2 μM. Licoisoflavone A and Licoisoflavone B inhibit copper-induced protein oxidative modification of mice brain homogenate in vitro. Synonyms: 2',4',5,7-Tetrahydroxy-3'-(3,3-dimethylallyl)isoflavone; 3-[2,4-Dihydroxy-3-(3-methyl-2-butenyl)phenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one; Phaseoluteone; 4H-1-Benzopyran-4-one, 3-[2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-5,7-dihydroxy-; 2',4',5,7-Tetrahydroxy-3'-(3,3-dimethylallyl)isoflavone; 3'-Isopentenyl-2',4',5,7-tetrahydroxyisoflavone. Grade: >95%. CAS No. 66056-19-7. Molecular formula: C20H18O6. Mole weight: 354.35. | |
| Licorice Extract | Licorice Extract. Alternative Names: D06811;Glycyrrhiza extract (jp15);Dry Licorice Root;Licorice Block Powder;Licorice extract liquid;glycyrrhiza;glycyrrhizae(latin);glycyrrhizaextract. CAS No. 68916-91-6. Product ID: PIPE-0804. EINECS: 272-837-1. Category: Natural Extract. |  |
| Licorice Extract | Licorice Extract. Applications: As a sweetener, licorice extract is used in food industry;as as raw materials of drugs for clearing heat and detoxicating, licorice extract is used in medicine field;as product for benefiting stomach, licorice extract is widely used in health industry;licorice extract applied in cosmetic field, licorice extract is able to nourish and cure the skin. Group: Others. Purity: 10%-98% Min. Appearance: Brown fine powder. Source: Liquorice, or licorice is the root of Glycyrrhiza glabra from which a sweet flavour can be extracted. The liquorice plant is a herbaceous perennial legume native to southern Europe, India, and parts of Asia. It is not botanically related to anise, star anise, or fennel, which are sources of similar flavouring compounds. Licorice Extract; Radix Glycyrrhizae. Cat No: EXTC-191. | |
| Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3% | Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3%. |  CA, FL & NJ |
| Lidanserin | Lidanserin (ZK-33839) acts as a 5-HT 2A and α 1 -adrenergic receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZK-33839. CAS No. 73725-85-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101815. | |
| L-iditol 2-dehydrogenase | This enzyme is widely distributed and has been described in archaea, bacteria, yeast, plants and animals. It acts on a number of sugar alcohols, including (but not limited to) L-iditol, D-glucitol, D-xylitol, and D-galactitol. Enzymes from different organisms or tissues display different substrate specificity. The enzyme is specific to NAD+ and can not use NADP+. Group: Enzymes. Synonyms: polyol dehydrogenase; sorbitol dehydrogenase; L-iditol:NAD+ 5-oxidoreductase; L-iditol (sorbitol) dehydrogenase; glucitol dehydrogenase; L-iditol:NAD+ oxidoreductase; NAD+-dependent sorbitol dehydrogenase; NAD+-sorbitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.14. CAS No. 9028-21-1. SDH. 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-0043; L-iditol 2-dehydrogenase; EC 1.1.1.14; 9028-21-1; polyol dehydrogenase; sorbitol dehydrogenase; L-iditol:NAD+ 5-oxidoreductase; L-iditol (sorbitol) dehydrogenase; glucitol dehydrogenase; L-iditol:NAD+ oxidoreductase; NAD+-dependent sorbitol dehydrogenase; NAD+-sorbitol dehydrogenase. Cat No: EXWM-0043. | |
| Lidocaine | Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine. CAS No. 137-58-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185. | |
| Lidocaine | Lidocaine. Group: Biochemicals. Alternative Names: Xylocaine; Lignocaine. Grades: Highly Purified. CAS No. 137-58-6. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C14H22N2O. US Biological Life Sciences. | Worldwide |
| Lidocaine Base USP | Lidocaine is a local anesthetic that works by causing temporary numbness/loss of feeling in the skin and mucous membranes. Uses: topically to relieve itching, burning, and pain from inflammatory skin conditions, injected as a dental anesthetic. Group: OTC (Over-the-Counter) Active Ingredients. INCI Name: Lidocaine Base USP. CAS Number: 137-58-6. |  United States and all of its trading partners.. |
| Lidocaine-d10 | Lidocaine-d 10 is the deuterium labeled Lidocaine. Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 851528-09-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185S1. | |
| Lidocaine-d10 hydrochloride | Lidocaine-d 10 (hydrochloride) is the deuterium labeled Lidocaine hydrochloride. Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride, an amide derivative, has the potential for the research of the ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1189959-13-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185AS. | |
| Lidocaine-d10 Hydrochloride (2- (Diethyl-d10-amino) -N- (2, 6-dimethylphenyl) acetamide Hydrochloride, Basicaina-d10, Batixim-d10, Dynexan-d10, Heweneural-d10, Licain-d10) | Anesthetic (local); antiarrhythmic (class IB). Group: Biochemicals. Alternative Names: 2- (Diethyl-d10-amino) -N- (2, 6-dimethylphenyl) acetamide Hydrochloride; Basicaina-d10; Batixim-d10; Dynexan-d10; Heweneural-d10; Licain-d10. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Lidocaine-d10 N-Oxide | A novel labeled metabolite of Lidocaine. Group: Biochemicals. Alternative Names: 2-[Di (ethyl-d5) oxidoamino]-N- (2, 6-dimethylphenyl) acetamide; 2-[Di(ethyl-d5)amino]-2',6'-acetoxylidide N-Oxide; 2-[Di (ethyl-d5) amino]-N- (2, 6-dimethylphenyl) acetamide N2-Oxide. Grades: Highly Purified. CAS No. 851528-10-4. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Lidocaine-d6 Hydrochloride | Lidocaine-d6 Hydrochloride is the labeled analogue of Lidocaine Hydrochloride, a local anesthetic; antiarrhythmic (class IB). Long-acting, membrane stabilizing agent against ventricular arrhythmia. Originally developed as a local anesthetic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C14H17D6ClN2O. US Biological Life Sciences. | Worldwide |
| Lidocaine EP Impurity E HCl | Lidocaine EP Impurity E HCl. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1135231-62-7. Molecular formula: C20H26ClN3O2. Mole weight: 375.9. Catalog: APB1135231627. | |
| Lidocaine HCL | Lidocaine HCL. Categories: lidocaine hydrochloride; 73-78-9. | CA, FL & NJ |
| Lidocaine HCL USP | Lidocaine is a local anesthetic that works by causing temporary numbness/loss of feeling in the skin and mucous membranes. Water soluble form of lidocaine. Uses: used topically to relieve itching, burning, and pain from inflammatory skin conditions, injected as a dental anesthetic. Group: OTC (Over-the-Counter) Active Ingredients. INCI Name: Lidocaine HCL. CAS Number: 6108-05-0. | United States and all of its trading partners.. |
| Lidocaine hydrochloride | Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride is an amide derivative and a agent to treat ventricular arrhythmia and an effective tumor-inhibitor [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride. CAS No. 73-78-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185A. | |
| Lidocaine hydrochloride hydrate | Lidocaine (Lignocaine) hydrochloride hydrate inhibits sodium channels involving complex voltage and using dependence. Lidocaine hydrochloride hydrate decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride hydrate is an amide derivative and has potential for the research of ventricular arrhythmia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride hydrate. CAS No. 6108-05-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B0185B. | |
| Lidocaine Hydrochloride Monohydrate | Lidocaine hydrochloride monohydrate is a commonly used as local anesthetic in topical applications and oral mucosal biopsies. It has a short anesthetic half-life; Na+ channel blocker; class IB antiarrhythmic that is rapidly absorbed after parenteral administration. Group: Biochemicals. Alternative Names: 2-(Diethylamino)-2',6'-acetoxylidide Hydrochloride; 2-(Diethylamino)-2',6'-dimethylacetanilide Hydrochloride; Alphacaine; DioCaine; Irtopan; Jetmonal; Lidesthesin; Lidocain Hydrochloride; Lidocaine Monohydrochloride; Lidothesin; Lignavet; Lignocaine Hydrochloride; Luan; Metaclopromide Hydrochloride; Odontalg; Proliferol; Rapidocaine; Sedagul; Versicane; Xilina Hydrochloride; Xycaine Hydrochloride; Xylanaest Purum; Xylocaine Astra; Xylocaine Hydrochloride; Xylocard; Xyloneural; Xylotox. Grades: Highly Purified. CAS No. 6108-05-0. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C14H23ClN2O, Molecular Weight: 288.81. US Biological Life Sciences. | Worldwide |
| Lidocaine Impurity 17 | Lidocaine Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-chloro-N-(2,6-dimethylphenyl)acetamide. CAS No. 1131-01-7. Molecular formula: C10H12ClNO. Mole weight: 197.66. Catalog: APB1131017. | |
| Lidocaine Impurity D | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidocaine Impurity Mixture solution | 20-200 ?g/mL in acetonitrile (each analyte), certified reference material, ampule of 1 mL. Group: Pharmaceutical impurities. | |
| Lidocaine N-ethyl chloride | Lidocaine N-ethyl chloride. Uses: For analytical and research use. Group: Fluorescence/luminescence spectroscopy. CAS No. 5369-3-9. Pack Sizes: 500MG, 1G. Mole weight: 298.85. Catalog: AP5369039. | |
| Lidocaine N-Oxide | A novel metabolite of Lidocaine. Group: Biochemicals. Alternative Names: 2- (Diethyloxidoamino) -N- (2, 6-dimethylphenyl) acetamide; 2-(Diethylamino)-2',6'-acetoxylidide N-Oxide; 2- (Diethylamino) -N- (2, 6-dimethylphenyl) acetamide N2-Oxide. Grades: Highly Purified. CAS No. 2903-45-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Lidocaine Related Compound B | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidocaine Related Compound E | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidocaine Related Compound H | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidocaine Related Compound H | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lidocaine Related Compound I | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidocaine Related Compound J | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impurities. | |
| Lidoflazine | Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K + channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3416-26-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-112075. | |
| Lidoflazine | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopyapi standardspharmaceutical toxicology. Alternative Names: McN-JR 7904, Corflazine, 4-[4,4-Bis(p-fluorophenyl)butyl]-1-piperazineaceto-2',6'-xylidide, 1-[4,4-Bis(fluorophenyl)butyl]-4-(2,6-dimethylanilinocarbonylmethyl)piperazine, Lidoflazine, Ordiflazine, Clinium, R 7904, Angex, Lidoflazinum, 1-[4,4-Bis(4-fluorophenyl)butyl]-4-(2,6-dimethylphenylcarbamoylmethyl)piperazine, Lidoflazin,1-Piperazineacetamide, 4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-, McN-JR 7094, Klinium, 1-[4,4-Di(4-fluorophenyl)butyl]-4-[(2,6-dimethylanilinocarbonyl)methyl]piperazine, 1-Piperazineaceto-2',6'-xylidide, 4-[4,4-bis(p-fluorophenyl)butyl]- (7CI,8CI). | |
| L-idonate 5-dehydrogenase | The enzyme from the bacterium Escherichia coli is specific for 5-dehydro-D-gluconate. cf. EC 1.1.1.366, L-idonate 5-dehydrogenase (NAD+). Group: Enzymes. Enzyme Commission Number: EC 1.1.1.264. CAS No. 211737-68-7. 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-0170; L-idonate 5-dehydrogenase; EC 1.1.1.264; 211737-68-7. Cat No: EXWM-0170. | |
| L-idonate 5-dehydrogenase (NAD+) | Involved in the catabolism of ascorbate (vitamin C) to tartrate. No activity is observed with NADP+ (cf. EC 1.1.1.264, L-idonate 5-dehydrogenase). Group: Enzymes. Enzyme Commission Number: EC 1.1.1.366. 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-0283; L-idonate 5-dehydrogenase (NAD+); EC 1.1.1.366. Cat No: EXWM-0283. | |
| L-idose-[1-13C] | A stable labelled analogue of L-idose. L-idose is the L-Isomer of D-idose. Synonyms: L-[1-13C]idose; L-idose-1-13C. Molecular formula: C5[13C]H12O6. Mole weight: 181.15. | |
| L-Idose-1-13C | L-Idose-1-13C. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-idose-[2-13C] | A stable labelled analogue of L-idose. L-idose is the L-Isomer of D-idose. Synonyms: L-[2-13C]idose; L-idose-2-13C. Molecular formula: C5[13C]H12O6. Mole weight: 181.15. | |
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