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| Product | Description | |
|---|---|---|
| L-Homoproline methyl ester hydrochloride | L-Homoproline methyl ester hydrochloride. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. |  Worldwide |
| L-Homoproline methyl ester hydrochloride | Synonyms: L-HomoPro-OMe HCl; L-Pipecolic acid methyl ester hydrochloride. Grades: ≥ 99% (HPLC). CAS No. 18650-39-0. Molecular formula: C7H13NO2·HCl. Mole weight: 179.62. |  |
| L-Homopropargylglycine | L-Homopropargylglycine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 98891-36-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-140345. |  |
| L-Homopropargylglycine | L-Homopropargylglycine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| L-Homopropargylglycine hydrochloride | L-Homopropargylglycine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine hydrochloride is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 942518-19-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-140345A. | |
| L-Homoserine | L-Homoserine. Group: Biochemicals. Alternative Names: 2-Amino-4-hydroxybutyric Acid; (S)-2-Amino-4-hydroxybutanoic Acid; NSC 206251. Grades: Highly Purified. CAS No. 672-15-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| L-Homoserine | Synonyms: L-HomoSer-OH; L-2-Amino-4-hydroxybutyric acid; (S)-2-Amino-4-hydroxybutyric acid; Butyric acid, 2-amino-4-hydroxy-, L-; (S)-2-Amino-4-hydroxybutanoic acid; (S)-Homoserine; Butanoic acid, 2-amino-4-hydroxy-, (S)-; Homoserine; NSC 206251. Grades: ≥95%. CAS No. 672-15-1. Molecular formula: C4H9NO3. Mole weight: 119.12. | |
| L-Homoserine | Homoserine. CAS No. 672-15-1. |  Pennsylvania PA |
| L-HomoSerine | L-HomoSerine. Uses: For analytical and research use. Group: Impurity standards. CAS No. 672-15-1. Molecular Formula: C4H9NO3. Mole Weight: 119.12. Catalog: APB672151. |  |
| L-Homoserine, 3-methyl- | L-Homoserine, 3-methyl-. Uses: For analytical and research use. Group: Impurity standards. CAS No. 906326-62-3. Molecular Formula: C5H11NO3. Mole Weight: 133.15. Catalog: APB906326623. | |
| L-Homoserine, 98+% | Identification: Meets specifications. Group: Biochemicals. Alternative Names: (S)-2-Amino-4-hydroxybutyric acid. Grades: Highly Purified. CAS No. 672-15-1. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| L-Homoserine lactone | L-Homoserine lactone (HSL), comprises a homoserine lactone ring and a fatty acyl side. The levels of L-Homoserine lactone in bacteria is dictated by the availability of the substrates and acyl-homoserine lactones synthase. Synonyms: (S)-3-aminodihydrofuran-2(3H)-one. CAS No. 2185-2-6. Molecular formula: C4H7NO2. Mole weight: 101.10. | |
| L-Homoserine lactone HCl | L-Homoserine lactone HCl. Group: Biochemicals. Alternative Names: (3S)-3-Aminodihydro-2(3H)-furanone hydrochloride; (S)-Homoserine lactone hydrochloride; L-Homoserine lactone hydrochloride. Grades: Highly Purified. CAS No. 2185-3-7. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C4H8ClNO2. US Biological Life Sciences. | Worldwide |
| L-Homoserine lactone HCl | Homoserine lactone HCl. CAS No. 2185-2-6. | Pennsylvania PA |
| L-Homoserine lactone hydrochloride | L-Homoserine lactone hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Peptides. CAS No. 2185-3-7. Pack Sizes: 25 g. Product ID: HY-W015800. | |
| L-Homoserine Lactone, Hydrochloride | Melting Point: 218-220°C. Group: Biochemicals. Grades: Highly Purified. CAS No. 2185-3-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| L-Homotyrosine hydrobromide salt | Synonyms: L-HomoTyr-OH HBr. Grades: ≥ 97% (NMR). CAS No. 141899-12-9. Molecular formula: C10H13NO3·HBr. Mole weight: 276.10. | |
| L-Homotyrosine hydrobromide salt ≥95% (HPLC) | L-Homotyrosine hydrobromide salt ≥95% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| LHRH (1-2) (free acid) | Synonyms: H-Pyr-His-OH; L-pyroglutamyl-L-histidine; Pyroglutamylhistidine; (S)-3-(1H-Imidazol-4-yl)-2-((S)-5-oxopyrrolidine-2-carboxamido)propanoic acid; 5-Oxo-L-prolyl-L-histidine; N-(5-Oxo-L-prolyl)-L-histidine. Grades: ≥95%. CAS No. 32159-22-1. Molecular formula: C11H14N4O4. Mole weight: 266.26. | |
| Lhrh(1-6)(free acid) | Lhrh(1-6)(free acid). Uses: Designed for use in research and industrial production. Additional or Alternative Names: PYR-HIS-TRP-SER-TYR-GLY-OH TRIFLUOROACETATE SALT;LUTEINIZING HORMONE-RELEASING HORMONE (1-6) TRIFLUOROACETATE SALT;LUTEINIZING HORMONE-RELEASING FACTOR (1-6) TRIFLUOROACETATE SALT;GONADOTROPIN-RELEASING HORMONE (1-6) TRIFLUOROACETATE SALT;LHRH (1-6) TRIF. Product Category: Heterocyclic Organic Compound. CAS No. 103067-73-8. Molecular formula: C36H41N9O10. Mole weight: 873.79. Product ID: ACM103067738. Alfa Chemistry ISO 9001:2015 Certified. Categories: LHRH (1-6) (free acid). |  |
| 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. Grades: 95%. CAS No. 47922-48-5. Molecular formula: C54H71N15O14. Mole weight: 1154.23. | |
| LHRH (free acid) | Synonyms: 10-Glycine-LHRH; 10-Gly-LHRH; LHRH, Glycine(10)-; pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly. 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. Grades: ≥95%. CAS No. 91097-16-4. Molecular formula: C60H69N17O13. Mole weight: 1236.32. | |
| LH secretion antagonist 1 | An antagonist of luteinising hormone secretion. Synonyms: 2,6-Methano-3-benzazocine-6,8(1H)-diol, 3-(3-butyn-1-yl)-2,3,4,5-tetrahydro-11,11-dimethyl-, hydrochloride. CAS No. 88531-67-3. Molecular formula: C18H24ClNO2. Mole weight: 321.84. | |
| LHW090-A7 sodium | LHW090-A7 is an inhibitor of neutral endopeptidase (NEP), an enzyme responsible for the metabolic inactivation of enkephalins. It has been shown to induce the increase of plasma levels of endogenous atrial natriuretic peptides (NPs). Synonyms: (S)-3-(3'-Chloro-[1,1'-biphenyl]-4-yl)-2-(((S)-1-ethoxy-1-oxopropan-2-yl)amino)propanoic sodium salt. Grades: ≥98%. Molecular formula: C20H21ClNO4·Na. Mole weight: 397.8. | |
| 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-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 nutrition and flavor enhancer. Synonyms: L-Proline, 4-hydroxy-, (4R)-; (4R)-4-Hydroxy-L-proline; L-Proline, 4-hydroxy-, trans-; Proline, 4-hydroxy-, L-; (-)-4-Hydroxy-2-pyrrolidinecarboxylic acid; (2S,4R)-(-)-4-Hydroxyproline; (2S,4R)-4-Hydroxyproline; (4R,2S)-Hydroxyproline; (R)-4-Hydroxy-(S)-proline; (R)-4-Hydroxy-L-proline; (S)-Hydroxyproline; 4(R)-Hydroxy-2(S)-pyrrolidinecarboxylic acid; 4(R)-Hydroxyproline; 4-Hydroxy-(S)-proline; 4-Hydroxy-L-proline; 4-Hydroxyproline; 4-trans-Hydroxy-L-proline; L-4-Hydroxyproline; L-Hypro; L-trans-4-Hydroxyproline; Hydroxy-L-proline; Hydroxyproline; Hypro; Ls-Hydroxyproline; NSC 46704; Proline, 4-hydroxy-; trans-(2S,4R)-4-Hydroxy-L-proline; trans-4-Hydroxy-L-proline; trans-4-Hydroxyproline; trans-L-4-Hydroxyproline; trans-L-Hydroxyproline; δ-Hydroxyproline. Grades: 98%. CAS No. 51-35-4. Molecular formula: C5H9NO3. Mole weight: 131.13. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | 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 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 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 hydrochloride | Liarozole hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 145858-50-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| 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 | 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 (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 | 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 |
| 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. | |
| 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. | |
| 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. | |
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