A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| 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-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-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 | Molecular formula: C11H16ClNO3. Mole weight: 245.7. |  |
| Liafensine | This active molecular is a SNDR (serotonin-norepinephrine-dopamine reuptake) inhibitor It was originated by Bristol-Myers Squibb for the treatment of major depressive disorder. In Feb 2013, Phase-II clinical trials in Major depressive disorder (treatment-experienced) in Argentina was on going. In May 2013, Bristol-Myers Squibb completed a phase II trial in Argentina, Australia, Austria, Canada, France, India, Italy, Puerto Rico, South Africa, Spain, United Kingdom and USA. In Oct 2013, Bristol-Myers Squibb discontinued a phase II trial in Major depressive disorder (treatment resistant) because of its increased capacity for side effects as well as potential for abuse. Uses: The treatment of major depressive disorder. Synonyms: 6-[(4S)-2-methyl-4-naphthalen-2-yl-3,4-dihydro-1H-isoquinolin-7-yl]pyridazin-3-amine;BMS-820836; BMS 820836; BMS820836; Liafensine. Grades: 98%. CAS No. 1198790-53-2. Molecular formula: C24H22N4. Mole weight: 366.47. | |
| Liangshanin A | Terpenoids. CAS No. 122717-54-8. Molecular formula: C20H26O4. Mole weight: 330.4. Appearance: Powder. Purity: 0.98. IUPACName: (1R, 2R, 4S, 9R, 10S, 13S, 16R)-2, 16-dihydroxy-5, 5, 9-trimethyl-14-methylidenetetracyclo[11.2.1.01, 10.04, 9]hexadec-7-ene-6, 15-dione. Canonical SMILES: CC1 (C2CC (C34C (C2 (C=CC1=O)C)CCC (C3O)C (=C)C4=O)O)C. Catalog: ACM122717548. |  |
| Liarozole | Heterocyclic Organic Compound. Alternative Names: Liarozole. CAS No. 115575-11-6. Molecular formula: C17H13ClN4. Mole weight: 308.771. Catalog: ACM115575116. | |
| Liarozole | This active molecular has a potential antineoplastic activity. As a retinoic acid metabolism blocking agent (RAMBA), liarozole inhibits P450-dependent ATRA-4-hydroxylase to an increase in endogenous ATRA production, inhibition of cell proliferation, and induction of cell differentiation. Meanwhile, liarozole also inhibits aromatase that catalyzes estrogen biosynthesis in rating-limited step. In Aug 2005, clinical development was ongoing for Ichthyosis in Europe.In Jan 2006, Phase-II/III clinical trials in Ichthyosis was ongoing in Europe and in Canada. Uses: Treatment for ichthyosis. Synonyms: 6-[(3-chlorophenyl)-imidazol-1-ylmethyl]-1H-benzimidazole, R 75251; R-75251; R75251. Grades: 98%. CAS No. 115575-11-6. Molecular formula: C17H13ClN4. Mole weight: 308.771. | |
| 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 | Liarozole dihydrochloride is a cytochrome P450 inhibitor. It displays antitumor activity against androgen-dependent and independent rat prostate carcinomas. Synonyms: 5-[(3-Chlorophenyl)-1H-imidazol-1-ylmethyl]-1H-benzimidazole dihydrochloride. Grades: ≥99% by HPLC. CAS No. 1883548-96-6. Molecular formula: C17H13ClN4.2HCl. Mole weight: 381.69. | |
| Liarozole hydrochloride | Liarozole is a benzimidazole derivative with potential antineoplastic activity. As a retinoic acid metabolism blocking agent (RAMBA), liarozole inhibits cytochrome P450-dependent all-trans-retinoic acid (ATRA)-4-hydroxylase, resulting in an increase in endogenous ATRA production, inhibition of cell proliferation, and induction of cell differentiation. This agent also inhibits aromatase, the enzyme that catalyzes the final, rate-limiting step in estrogen biosynthesis. Synonyms: Liarozole HCl; R75251 (hydrochloride); 5-((3-chlorophenyl)(1H-imidazol-1-yl)methyl)-1H-benzo[d]imidazole hydrochloride. CAS No. 145858-50-0. Molecular formula: C17H14Cl2N4. Mole weight: 345.23. | |
| Liarozole hydrochloride | Liarozole hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 145858-50-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| Libenzapril | Heterocyclic Organic Compound. CAS No. 109214-55-3. Molecular formula: C18H25N3O5. Mole weight: 363.408 g/mol. Purity: 0.96. IUPACName: (2S)-6-amino-2-[[(3S)-1-(carboxymethyl)-2-oxo-4,5-dihydro-3H-1-benzazepin-3-yl]amino]hexanoic acid. Density: 1.33g/cm³. Catalog: ACM109214553. | |
| Liberine | Liberine is one of Caffeine metabolites. Caffeine is a CNS stimulant. Alkaloid, purified from plants of Coffea genus, Rubiaceae. Synonyms: O2,1,9-Trimethyluric Acid; 7,9-Dihydro-2-methoxy-1,9-dimethyl-1H-purine-6,8-dione; 2-Methoxy-1,9-dimethyl-1H-purine-6,8(7H,9H)-dione; O(2),1,9-trimethylurate; 2-methoxy-1,9-dimethyl-6,7,8,9-tetrahydro-1H-purine-6,8-dione. Grades: 98%. CAS No. 56119-16-5. Molecular formula: C8H10N4O3. Mole weight: 210.19. | |
| 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 | Organic Light Emitting Diode (OLED). Alternative Names: Lithium 2-(2', 2''-bipyridine-6'-yl)phenolate. CAS No. 1049805-81-3. Molecular formula: C16H11LiN2O. Mole weight: 254.21 g/mol. Catalog: ACM1049805813. | |
| 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 (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. Group: Inhibitors. CAS No. 51020-86-1. Molecular formula: C20H22O4. Mole weight: 326.39. Appearance: Solid. 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. Catalog: ACM51020861. | |
| Licarin A | Cas No. 51020-86-1. | |
| 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 |
| Lichenan - from Cetraria islandica | Cas No. 1402-10-4. | |
| 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. | |
| Lichen Extract | Extract obtained from Usnea Barbata (Lichen) plants. Contains 20% extract dissolved in water and glycerin. Has purifying, cleansing, and soothing properties. Uses: Moisturizing creams and lotions, cleaners, toners and astringents. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84696-53-7 / 122-99-6. Appearance: Light to medium yellow liquid, characteristic odor. Catalog: CI-SC-0849. | |
| 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. | |
| 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. | |
| 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 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. | |
| 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 is a dual inhibitor of COX-1/COX-2 and 5-lipoxygenase. Uses: Lipoxygenase inhibitors. Synonyms: ML 3000; ML3000; ML-3000; 6-(4-chlorophenyl)-2,3-dihydro-2,2-dimethyl-7-phenyl-1H-pyrrolizine-5-acetic acid. CAS No. 156897-06-2. Molecular formula: C23H22ClNO2. Mole weight: 379.9. | |
| 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 |
| Licoflavanone | Flavonoids. CAS No. 119240-82-3. Molecular formula: C20H20O5. Mole weight: 340.4. Appearance: Powder. Purity: 0.98. IUPACName: 5,7-dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one. Canonical SMILES: CC (=CCC1=C (C=CC (=C1)C2CC (=O)C3=C (C=C (C=C3O2)O)O)O)C. Catalog: ACM119240823. | |
| 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. Group: Inhibitors. CAS No. 91433-17-9. Molecular formula: C25H26O4. Mole weight: 390.47. Appearance: Solid. 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. Catalog: ACM91433179. | |
| 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 |
| Licopyranocoumarin | Flavonoids. CAS No. 117038-80-9. Molecular formula: C21H20O7. Mole weight: 384.38. Appearance: Powder. Purity: 0.98. IUPACName: 7-(2,4-dihydroxyphenyl)-2-(hydroxymethyl)-5-methoxy-2-methyl-3,4-dihydropyrano[3,2-g]chromen-8-one. Canonical SMILES: CC1 (CCC2=C (O1)C=C3C (=C2OC)C=C (C (=O)O3)C4=C (C=C (C=C4)O)O)CO. Catalog: ACM117038809. | |
| 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 Extract | Natural extract of licorice roots (glycyrrhiza glabra) in a base of glycerin and water. Licorice is native to the mediterranean region. Contains 20% of extract. Uses: Creams, lotions, and all kinds of skin-lightening products. Group: Skin actives. CAS No. 56-81-5 / 7732-18-5 / 84775-66-6 / 122-99-6. Appearance: Amber liquid, characteristic odor. Catalog: CI-SC-0679. | |
| Licorice Extract in Safflower Oil | Natural extract of licorice roots (glycyrrhiza glabra) dissolved in a base of safflower oil which contains 71.0 - 84.0% of linoleic acid C18:2. Licorice is native to the mediterranean region. Contains 20% of extract. Uses: Creams, lotions, and all kinds of skin-lightening products. Group: Emollients/oils/wax. CAS No. 8001-23-8/84775-66-6/7695-91-2. Appearance: Amber liquid, characteristic odor. Catalog: CI-SC-0461. | |
| Licorice Extract, USDA Certified Organic | Organic extract of licorice roots (glycyrrhiza glabra). Licorice is native to the Mediterranean region. Contains 20% extract dissolved in glycerin. Uses: Creams, lotions, and all kinds of skin- lightening products. Group: Skin actives. CAS No. 56-81-5/84775-66-6. Appearance: Colorless, odorless, viscous liquid. Catalog: CI-SC-0706. | |
| Licorice Root Extract | Licorice root extract is produced from the roots and rhizomes of the Glycyrrhiza glabra. A multi-functional botanical, the polysaccharide fraction has shown remarkable immunomodulatory activity, stimulating cell regeneration and hence anti-aging properties. The polysaccharides, triterpene saponins and flavonoids contained in this extract enable formulations in these areas: Anti-irritants, antimicrobials, photo-protectors, hair color protectors and inhibition of tyrosinase/skin depigmentation. Uses: Anti-irritants, antimicrobials, photo-protectors, hair color protectors and inhibition of tyrosinase/skin depigmentation. Group: Skin actives. CAS No. 56-81-5/7732-18-5/84775-66-6. Catalog: CI-SC-0678. | |
| Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3% | Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3%. |  CA, FL & NJ |
| Licoricesaponin A3 | Terpenoids. CAS No. 118325-22-7. Molecular formula: C48H72O21. Mole weight: 985.07. Appearance: Powder. Purity: 0.98. IUPACName: (2S, 3S, 4S, 5R, 6R)-6-[(2R, 3R, 4S, 5S, 6S)-2-[[(3S, 4aR, 6aR, 6bS, 8aS, 11S, 12aR, 14aR, 14bS)-4, 4, 6a, 6b, 8a, 11, 14b-heptamethyl-14-oxo-11-[(2S, 3R, 4S, 5S, 6R)-3, 4, 5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2, 3, 4a, 5, 6, 7, 8, 9, 10, 12, 12a, 14a-dodecahydro-1H-picen-3-yl]oxy]-6-carboxy-4, 5-dihydroxyoxan-3-yl]oxy-3, 4, 5-trihydroxyoxane-2-carboxylic acid. Canonical SMILES: CC1 (C2CCC3 (C (C2 (CCC1OC4C (C (C (C (O4)C (=O)O)O)O)OC5C (C (C (C (O5)C (=O)O)O)O)O)C)C (=O)C=C6C3 (CCC7 (C6CC (CC7) (C)C (=O)OC8C (C (C (C (O8)CO)O)O)O)C)C)C)C. Catalog: ACM118325227. | |
| Licoricesaponin E2 | Terpenoids. CAS No. 119417-96-8. Molecular formula: C42H60O16. Mole weight: 820.92. Appearance: Powder. Purity: 0.98. Canonical SMILES: CC1 (C2CCC3 (C (C2 (CCC1OC4C (C (C (C (O4)C (=O)O)O)O)OC5C (C (C (C (O5)C (=O)O)O)O)O)C)C (=O)C=C6C3 (CCC7 (C6CC8 (CC7OC8=O)C)C)C)C)C. Catalog: ACM119417968. | |
| Licoricesaponin G2 | Terpenoids. CAS No. 118441-84-2. Molecular formula: C42H62O17. Mole weight: 838.93. Appearance: Powder. Purity: 0.98. IUPACName: (2S, 3S, 4S, 5R, 6R)-6-[(2R, 3R, 4S, 5S, 6S)-2-[[(3S, 4S, 4aR, 6aR, 6bS, 8aS, 11S, 12aR, 14aR, 14bS)-11-carboxy-4-(hydroxymethyl)-4, 6a, 6b, 8a, 11, 14b-hexamethyl-14-oxo-2, 3, 4a, 5, 6, 7, 8, 9, 10, 12, 12a, 14a-dodecahydro-1H-picen-3-yl]oxy]-6-carboxy-4, 5-dihydroxyoxan-3-yl]oxy-3, 4, 5-trihydroxyoxane-2-carboxylic acid. Canonical SMILES: CC12CCC (CC1C3=CC (=O)C4C5 (CCC (C (C5CCC4 (C3 (CC2)C)C) (C)CO)OC6C (C (C (C (O6)C (=O)O)O)O)OC7C (C (C (C (O7)C (=O)O)O)O)O)C) (C)C (=O)O. Catalog: ACM118441842. | |
| Licoricesaponin H2(18Beta,20Alpha-Glycyrrhizic Acid) | Terpenoids. CAS No. 118441-85-3. Molecular formula: C42H62O16. Mole weight: 822.92. Appearance: Powder. Purity: 0.98. IUPACName: (2S, 3S, 4S, 5R, 6R)-6-[(2R, 3R, 4S, 5S, 6S)-2-[[(3S, 4aR, 6aR, 6bS, 8aS, 11R, 12aR, 14aR, 14bS)-11-carboxy-4, 4, 6a, 6b, 8a, 11, 14b-heptamethyl-14-oxo-2, 3, 4a, 5, 6, 7, 8, 9, 10, 12, 12a, 14a-dodecahydro-1H-picen-3-yl]oxy]-6-carboxy-4, 5-dihydroxyoxan-3-yl]oxy-3, 4, 5-trihydroxyoxane-2-carboxylic acid. Canonical SMILES: CC1 (C2CCC3 (C (C2 (CCC1OC4C (C (C (C (O4)C (=O)O)O)O)OC5C (C (C (C (O5)C (=O)O)O)O)O)C)C (=O)C=C6C3 (CCC7 (C6CC (CC7) (C)C (=O)O)C)C)C)C. Catalog: ACM118441853. | |
| Licorisoflavan A | Flavonoids. CAS No. 129314-37-0. Molecular formula: C27H34O5. Mole weight: 438.6. Appearance: Powder. Purity: 0.98. IUPACName: 4-[(3R)-5,7-dimethoxy-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methylbut-2-enyl)benzene-1,3-diol. Canonical SMILES: CC (=CCC1=C (C=CC (=C1O)C2CC3=C (C (=C (C=C3OC2)OC)CC=C (C)C)OC)O)C. Catalog: ACM129314370. | |
| 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-Idaric acid | L-Idaric acid is a promising compound for biomedical applications in research of microbial invasions, assuming a prominent role as the chief constituent in studying a diverse gamut of afflictions, ranging from bacterial infections to fungal maladies. Synonyms: L-idaric acid; 80876-58-0; Discontinued See I164930; (2R,3S,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid; SCHEMBL15895451; CHEBI:21333; W-203842; Q27109388. CAS No. 80876-58-0. Molecular formula: C6H10O8. Mole weight: 210.14. | |
| L-Idaric acid 1,4-lactone | L-Idaric acid 1,4-lactone, an esteemed biomedicine with a myriad of applications, unveils its profound therapeutic prowess in the vast realm of medical science. Renowned for its exquisite antioxidant attributes and tantalizing potential in combating cancer, this compound entices researchers and drug developers alike, beckoning them to unravel its enigmatic therapeutic effects that navigate the intricate labyrinth of specific malignancies and afflictions tormenting the delicate harmony of oxidative stress-induced conditions. Synonyms: L-Idaro-1,4-lactone. CAS No. 80876-59-1. Molecular formula: C6H8O7. Mole weight: 192.12. | |
Our database is helping our users find suppliers everyday.
