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| Product | Description | |
|---|---|---|
| LHRH (chicken) | It is a luteinizing hormone-releasing hormone (LHRH) that stimulates the anterior pituitary to release gonadotropins, thereby regulating reproductive function. Synonyms: H-Pyr-His-Trp-Ser-Tyr-Gly-Leu-Gln-Pro-Gly-NH2; L-pyroglutamyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-glycyl-L-leucyl-L-glutaminyl-L-prolyl-glycinamide; [Gln8]-C517 (LH-RH), chicken; 8-Glutamine-LHRH; GNRH, Chicken I; 8-Gln-LHRH; LHRH-I; pGlu-His-Trp-Ser-Tyr-Gly-Leu-Gln-Pro-Gly-NH2. Grade: 95%. CAS No. 47922-48-5. Molecular formula: C54H71N15O14. Mole weight: 1154.23. |  |
| LHRH (free acid) | LHRH (free acid), also known as Luteinizing Hormone-Releasing Hormone free acid, is a neuropeptide that plays a crucial role in regulating reproduction. This hormone is secreted by the hypothalamus and acts on the anterior pituitary gland to stimulate the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which are essential for reproductive functions. Synonyms: Glp-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly; H-Pyr-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-OH; 10-Glycine-luteinizing hormone-releasing factor (swine); 10-Glycine-luteinizing hormone-releasing factor (pig); 10-Glycine-LH-RH; [Gly-OH10]-LHRH; LH-RH(OH); LHRH acid; PGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly; LHRH free acid; L-Pyroglutamyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-glycyl-L-leucyl-L-arginyl-L-prolyl-glycine; XHWSYGLRPG. Grade: ≥95%. CAS No. 35263-73-1. Molecular formula: C55H74N16O14. Mole weight: 1183.27. | |
| LHRH free acid | LHRH (free acid), the luteinizing hormone-releasing hormone, is a neuropeptide hypothalamic. LHRH regulates reproduction. LHRH can be used for the research of cancer [1]. Uses: Scientific research. Group: Peptides. CAS No. 35263-73-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4675. |  |
| LHRH II | LHRH II, first found in chicken, is highly conserved in vertebrates. Synonyms: LH-RH II, chicken; Pyr-His-Trp-Ser-His-Gly-Trp-Tyr-Pro-Gly-NH2; LHRH, His(5)-Trp(7)-Tyr(8)-; Glycinamide, 5-oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-histidylglycyl-L-tryptophyl-L-tyrosyl-L-prolyl-; 5-Oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-histidylglycyl-L-tryptophyl-L-tyrosyl-L-prolylglycinamide; L-pyroglutamyl-L-histidyl-L-tryptophyl-L-seryl-L-histidyl-glycyl-L-tryptophyl-L-tyrosyl-L-prolyl-glycinamide; GNRH, Chicken II; pGlu-His-Trp-Ser-His-Gly-Trp-Tyr-Pro-Gly-NH2; 5-Histidyl-7-tryptophyl-8-tyrosine-LHRH; Luteinizing hormone-releasing factor II (chicken); cGnRH II. Grade: ≥95%. CAS No. 91097-16-4. Molecular formula: C60H69N17O13. Mole weight: 1236.32. | |
| L-Hydroorotic acid 98+% | L-Hydroorotic acid 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences. |  Worldwide |
| L-Hydroxy arginine acetate | L-Hydroxy arginine acetate is an intermediate in the catabolism of L-arginine. L-Hydroxy arginine acetate is a substrate for NO synthase [1]. Uses: Scientific research. Group: Peptides. CAS No. 1140844-61-6. Pack Sizes: 1 mg. Product ID: HY-115411. | |
| L-Hydroxy arginine dihydrochloride | L-Hydroxy arginine dihydrochloride is an intermediate in the catabolism of L-arginine, and is a substrate for NO synthase [1]. Uses: Scientific research. Group: Peptides. CAS No. 133565-48-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-115411A. | |
| L-?-Hydroxyglutaric acid disodium salt | ?98.0% (GC). Group: Fluorescence/luminescence spectroscopy. |  |
| L-Hydroxyproline | L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. Uses: Scientific research. Group: Natural products. Alternative Names: (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid. CAS No. 51-35-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g. Product ID: HY-40135. | |
| L-Hydroxyproline | (2S,4R)-4-Hydroxyproline, or L-hydroxyproline (C5H9O3N), is a common non-proteinogenic amino acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: L-Trans-4-hydroxy-L-proline. Product Category: Heterocyclic Organic Compound. Appearance: Solid. CAS No. 51-35-4. Molecular formula: C5H9NO3. Mole weight: 131.13. Purity: 0.98. IUPACName: (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid. Canonical SMILES: C1C(CNC1C(=O)O)O. Density: 1.3121 g/cm³. Product ID: ACM51354. Alfa Chemistry ISO 9001:2015 Certified. |  |
| L-Hydroxyproline | L-Hydroxyproline is an amino acid. It can be used as a nutrition and a flavor enhancer. Uses: L-hydroxyproline, also known as 4-hydroxyproline, is a non-protein amino acid that plays a vital role in the structure and function of collagen, the most abundant protein in the human body. in recent years, researchers have been exploring the potential applications of l-hydroxyproline in drug discovery and development due to its unique properties and biological activity. first and foremost, it is. Synonyms: trans-4-Hydroxy-L-proline; L-4-hydroxyproline; trans-4-Hydroxyproline; H-Hyp-OH; hydroxy-L-proline; 4-Hydroxy-L-proline; trans-L-Hydroxyproline; 4-Hydroxy-2-pyrrolidinecarboxylic acid. Grade: 98%. CAS No. 51-35-4. Molecular formula: C5H9NO3. Mole weight: 131.13. | |
| L-Hydroxy proline | L-Hydroxy proline. CAS No: 51-35-4 |  Sarchem Laboratories New Jersey NJ |
| L-Hydroxy proline | L-hydroxyproline is a common non-standard protein amino acid, which has high application value as the main raw material of antiviral drug azanavir. L-hydroxychemicalbookyl proline is generally used as a food additive (used as a sweetener, the amount is relatively small), and the intermediate used as penan side chain in medicine is relatively large. Synonyms: H-HYP-OH;H-HYP-OH (TRANS);H-L-HYDROXYPROLINE;H-L-HYP-OH;H-TRANS-HYP-OH;HYDROXYPROLINE;HYDROXY-L-PROLINE;HYDROXY-L-PROLINE, TRANS-4-. CAS No. 51-35-4. Product ID: PAP-0034. Molecular formula: C5H9NO3. Category: Amino acid. Product Keywords: Amino Acid Series; L-Hydroxy proline; PAP-0034; Amino acid; C5H9NO3; 51-35-4. Appearance: Crystals or Crystalline Powder. Chemical Name: L-Hydroxyproline. Grade: Pharmaceutical Grade. Solubility: H2O: 50 mg/mL. Storage: Store below +30°C. Boiling Point: 242.42°C (rough estimate). Melting Point: 273 °C (dec.)(lit.). Density: 1.3121 (rough estimate). Product Description: L-hydroxyproline is a common non-standard protein amino acid, which has high application value as the main raw material of antiviral drug azanavir. L-hydroxychemicalbookyl proline is generally used as a food additive (used as a sweetener, the amount is relatively small), and the intermediate used as penan side chain in medicine is relatively large. |  |
| L-Hydroxyproline (Standard) | L-Hydroxyproline (Standard) is the analytical standard of L-Hydroxyproline. This product is intended for research and analytical applications. L-Hydroxyproline, one of the hydroxyproline (Hyp) isomers, is a useful chiral building block in the production of many pharmaceuticals. Uses: Scientific research. Group: Natural products. CAS No. 51-35-4. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-40135R. | |
| L-Hydroxyprolylglycine | L-Hydroxyprolylglycine. Synonyms: Hyp-Gly; 4beta-Hydroxy-L-Pro-Gly-OH. Grade: 95%. CAS No. 7672-35-7. Molecular formula: C7H12N2O4. Mole weight: 188.18. | |
| L-Hyoscyamine | L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Hyoscyamine. CAS No. 101-31-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0471. | |
| L-Hyp(OEt)-OH HCl | L-Hyp(OEt)-OH HCl. Molecular formula: C11H16ClNO3. Mole weight: 245.7. | |
| Li2PC | Li2PC. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DILITHIUM PHTHALOCYANINE;LITHIUM PHTHALOCYANINE;29H,31H-PHTHALOCYANINE DILITHIUM SALT;PHTHALOCYANINE DILITHIUM;PHTHALOCYANINE, LI;PHTHALOCYANINE LITHIUM;Phthalocyanine Dilithium (contains ca. 20% 1-Pentanol);DilithiumPhthalocyanine(containsca.20%1-Pentano. Product Category: Photonic and Optical Device. CAS No. 25510-41-2. Molecular formula: C32H16Li2N8. Mole weight: 526.41. Purity: >93.0%(N). Product ID: ACM25510412. Alfa Chemistry ISO 9001:2015 Certified. Categories: Lipcani. | |
| Liangshanin A | Liangshanin A is a natural diterpenoid found in the herbs of Rabdosia bulleyana. Synonyms: Kaura-1,16-diene-3,15-dione, 7,14-dihydroxy-, (7a,14R)-. Grade: >98%. CAS No. 122717-54-8. Molecular formula: C20H26O4. Mole weight: 330.4. | |
| Liarozole | Liarozole (R75251; R85246) is an imidazole derivative and orally active retinoic acid (RA) metabolism-blocking agent (RAMBA). Liarozole inhibits the cytochrome P450 (CYP26)-dependent 4-hydroxylation of retinoic acid ( IC 50 =7 μM), resulting in increased tissue levels of retinoic acid. Liarozole shows antitumoral properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R75251. CAS No. 115575-11-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106019. | |
| Liarozole dihydrochloride | Liarozole (R75251) dihydrochloride is an imidazole derivative and orally active retinoic acid (RA) metabolism-blocking agent (RAMBA). Liarozole dihydrochloride inhibits the cytochrome P450 (CYP26)-dependent 4-hydroxylation of RA ( IC 50 =7 μM), resulting in increased tissue levels of RA. Liarozole dihydrochloride shows antitumoral properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R75251 dihydrochloride. CAS No. 1883548-96-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-106019C. | |
| Liarozole dihydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Liarozole hydrochloride | Liarozole hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 145858-50-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| LIBOB | LIBOB. Group: other electronic materials. CAS No. 244761-29-3. Product ID: lithium; 1,4,6,9-tetraoxa-5-boranuidaspiro[4.4]nonane-2,3,7,8-tetrone. Molecular formula: 193.8g/mol. Mole weight: C4BLiO8. [Li+]. [B-]12(OC(=O)C(=O)O1)OC(=O)C(=O)O2. InChI=1S/C4BO8. Li/c6-1-2 (7)11-5 (10-1)12-3 (8)4 (9)13-5; /q-1; +1. NVQAYVUCVASGDK-UHFFFAOYSA-N. |  |
| Libpp | Libpp. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Lithium 2-(2', 2''-bipyridine-6'-yl)phenolate. Product Category: Organic Light Emitting Diode (OLED). CAS No. 1049805-81-3. Molecular formula: C16H11LiN2O. Mole weight: 254.21 g/mol. Product ID: ACM1049805813. Alfa Chemistry ISO 9001:2015 Certified. Categories: Libjpeg. | |
| Licaminlimab | Licaminlimab (OCS-02) is a single-chain anti-TNF alpha antibody fragment. TNF alpha is an inflammatory cytokine produced by macrophages and monocytes during inflammation [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: OCS-02. CAS No. 1688648-13-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99704. | |
| Licarbazepine | Licarbazepine. Group: Biochemicals. Grades: Purified. CAS No. 29331-92-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Licarbazepine | Licarbazepine (BIA 2-005; GP 47779) is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BIA 2-005; GP 47779. CAS No. 29331-92-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108506. | |
| Licarbazepine-[d4] | Licarbazepine-[d4] is the labelled analogue of Licarbazepine, which is a metabolite of Oxcarbazepine. Synonyms: 10,11-Dihydro-10-hydroxy Carbamazepine-D4; 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carboxamide-D4; 10-Hydroxy-10,11-dihydrocarbamezepine-D4; Licarbazepine-D4. Grade: ≥97% by HPLC; ≥97% atom D. CAS No. 1020719-39-4. Molecular formula: C15H10D4N2O2. Mole weight: 258.32. | |
| Licarbazepine (Standard) | Licarbazepine (Standard) is the analytical standard of Licarbazepine. This product is intended for research and analytical applications. Licarbazepine (BIA 2-005; GP 47779) is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 29331-92-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108506R. | |
| Licarin A | Licarin A ((+)-Licarin A), a neolignan, significantly and dose-dependently reduces TNF-α production (IC50=12.6 μM) in dinitrophenyl-human serum albumin (DNP-HSA)-stimulated RBL-2H3 cells. Anti-allergic effects. Licarin A reduces TNF-α and PGD2 production, and COX-2 expression. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 51020-86-1. Molecular formula: C20H22O4. Mole weight: 326.39. Purity: 0.98. Canonical SMILES: OC1=CC=C([C@@H]2OC3=C(OC)C=C(/C=C/C)C=C3[C@H]2C)C=C1OC. Product ID: ACM51020861. Alfa Chemistry ISO 9001:2015 Certified. Categories: Lisa Rinna. | |
| Licarin A | Licarin A. Group: Biochemicals. Grades: Plant Grade. CAS No. 51020-86-1. Pack Sizes: 5mg. Molecular Formula: C20H22O4, Molecular Weight: 326.39. US Biological Life Sciences. | Worldwide |
| Lichenase 16A from Bacillus halodurans, 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-glucan. Enzyme Commission Number: EC 3.2.1.73. CAS No. 37288-51-0. Purity: >90% by SDS-PAGE. β-glucanase. Mole weight: 28.8 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 halodurans. 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-1420. |  |
| 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. 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 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 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 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. Group: Biochemicals. CAS No. 58749-23-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 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, 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. | |
| Licoisoflavone A | Licoisoflavone A. Group: Biochemicals. CAS No. 66056-19-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 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. | |
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