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| Product | Description | |
|---|---|---|
| LAC2-IBCA | Synonyms: [1-(Benzyl-methyl-carbamoyl)-2-methoxy-ethyl]-carbamic acid isobutyl ester. Grades: > 95%. Molecular formula: C16H24N2O4. Mole weight: 308.38. |  |
| LAC2 NMBA Impurity | Synonyms: 2-Acetylamino-N-benzyl-3-methoxy-N-methyl-propionamide. Grades: > 95%. Molecular formula: C14H20N2O3. Mole weight: 264.33. | |
| LACCAIC ACID | LACCAIC ACID. Synonyms: Shellac red color;Red Lac;froM Lacca;Laccaic Acid ;lac dye red;Purple sweet potato pigment;Water-soluble shellac red;c.i.75450. CAS No. 60687-93-6. Pack Sizes: 1 g. Product ID: CDF4-0025. Molecular formula: C91H62N2O44. Category: Color Fixative. Product Keywords: Food Ingredients; Color Fixative; LACCAIC ACID; CDF4-0025; 60687-93-6; C91H62N2O44; 918-731-7; 60687-93-6. Purity: 0.99. Color: Red to Very Dark Red. EC Number: 918-731-7. Physical State: Solid. Solubility: Aqueous Base (Slightly), DMSO (Slightly). Storage: -20°C Freezer, Under inert atmosphere. Application: Laccaic acid is an organic dye with antimicrobial properties towards various pathogenic bacteria and fungi. Laccaic acid is also used as a component of solar cells due to its photoelectric properties. Boiling Point: 453.24°C (rough estimate). Density: 1.4363 (rough estimate). |  |
| Laccaic acid a | Laccaic acid a. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LACCAIC ACID A;LACCAIC ACID A STANDARD;7-[2-Hydroxy-5-[2-(acetylamino)ethyl]phenyl]-3,5,6,8-tetrahydroxy-9,10-dioxo-9,10-dihydro-1,2-anthracenedicarboxylic acid;7-[5-[2-(Acetylamino)ethyl]-2-hydroxyphenyl]-9,10-dihydro-3,5,6,8-tetrahydroxy-9,10-dioxo-1,2-anthracenedicarboxylic acid. Product Category: Heterocyclic Organic Compound. CAS No. 15979-35-8. Molecular formula: C26H19NO12. Mole weight: 537.43. Product ID: ACM15979358. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Laccaic acid e | Laccaic acid e. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Laccaic acid E. Product Category: Heterocyclic Organic Compound. CAS No. 14597-16-1. Mole weight: 0. Product ID: ACM14597161. Alfa Chemistry ISO 9001:2015 Certified. | |
| Laccaridione A | It is produced by the strain of Laccaria amethystea. It can inhibit the activity of antiserine protease. It inhibits trypsin, papain, thermophilic protease, collagenase and zinc protease with IC50 (μg/mL) of 14.7, 2.5, 18.8, 7.2 and 18.2, respectively. Synonyms: 10-hydroxy-1,7-dimethoxy-3-[(2E)-4-methylhex-2-en-2-yl]-1H-benzo[g]isochromene-8,9-dione; 1H-Naphtho(2,3-C)pyran-8,9-dione, 3-((1E)-1,3-dimethyl-1-penten-1-yl)-10-hydroxy-1,7-dimethoxy-. CAS No. 320369-80-0. Molecular formula: C22H24O6. Mole weight: 384.42. | |
| Laccaridione B | It is produced by the strain of Laccaria amethystea. It can inhibit the activity of antiserine protease. It inhibits trypsin, papain, thermophilic protease, collagenase and zinc protease with IC50 (μg/mL) of 10.9, 5.1, 8.4, 5.7 and 3.0, respectively. It also has a strong anti-proliferative activity against L-929, K-562 and HeLa cells with IC50 (μg/mL) of 2.4, 1.8 and 13.9, respectively. Synonyms: 1-ethoxy-10-hydroxy-7-methoxy-3-[(2E)-4-methylhex-2-en-2-yl]-1H-benzo[g]isochromene-8,9-dione; 1H-Naphtho[2,3-c]pyran-8,9-dione, 3-[(1E)-1,3-dimethyl-1-pentenyl]-1-ethoxy-10-hydroxy-7-methoxy-. CAS No. 320369-81-1. Molecular formula: C23H26O6. Mole weight: 398.45. | |
| laccase | A group of multi-copper proteins of low specificity acting on both o- and p-quinols, and often acting also on aminophenols and phenylenediamine. The semiquinone may react further either enzymically or non-enzymically. Group: Enzymes. Synonyms: urishiol oxidase; urushiol oxidase; p-diphenol oxidase. Enzyme Commission Number: EC 1.10.3.2. CAS No. 80498-15-3. Laccase. 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-0482; laccase; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase. Cat No: EXWM-0482. |  |
| Laccase | Laccase. Synonyms: Denilase ii s;Novozyme 809;p-Diphenol oxidase;Sp 504;Urushiol oxidase;Laccase from Rhus vernicifera,Benzenediol:oxygen oxidoreductase;Laccase, from Trametes versicolor, >=0.5units/mg;LACCASE FROM TRAMETES SPEC., 0.8+ UMG POWDER. CAS No. 80498-15-3. Pack Sizes: 1 kg. Product ID: CDF4-0053. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; Laccase; CDF4-0053; 80498-15-3; 420-150-4; 80498-15-3. Purity: 0.99. Color: Slightly beige. EC Number: 420-150-4. Physical State: Powder. Storage: 2-8°C. Application: Laccase is polyphenol oxidase found in many plants, fungi and microorganisms. Laccases may be useful in enzymatic biofuel systems, teeth whitening, textile dyeing, and in other applications that require the removal of oxygen. Density: 1.37[at 20°C]. Product Description: Laccase is a kind of copper-containing oxidase existing in many kinds of plants, fungi and microbes. It mainly takes effect on phenol-like compounds including phenols, polyphenols and anilines, performing one-electron oxidation. | |
| LACCASE | Synonyms: EC 1.10.3.2; LACC; LACCASE; LACCASE AB; LACCASE, CORIOLUS VERSICOLOR, CLEA; LACCASE, CORIOLUS VERSICOLOR, CROSS-LINKED ENZYME AGGREGATE; LACCASE CV; LACCASE T. Grades: 95%. CAS No. 80498-15-3. | |
| Laccase from Agaricus bisporus | powder, deep brown, ?4 U/mg. Group: Fluorescence/luminescence spectroscopy. |  |
| Laccase from Bacillus subtilis, Recombinant | Laccase is a blue copper oxidase that reduces molecular oxygen to water. Laccase oxidizes polyphenols, methoxy-substituted phenols and diamines, but not tyrosine. Oxidation by laccase is an one-electron reaction that generates a free radical. Group: Enzymes. Synonyms: Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Purity: >90% as judged by SDS-PAGE. Laccase. Mole weight: 60.5 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: Bacillus subtilis. Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Cat No: NATE-1570. | |
| Laccase from Escherichia coli, Recombinant | Laccase is a blue copper oxidase that reduces molecular oxygen to water. Laccase oxidizes polyphenols, methoxy-substituted phenols and diamines, but not tyrosine. Oxidation by laccase is an one-electron reaction that generates a free radical. Group: Enzymes. Synonyms: Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Enzyme Commission Number: EC 1.10.3.-. Purity: >90% as judged by SDS-PAGE. Laccase. Mole weight: 55.4 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: Escherichia coli. Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Cat No: NATE-1569. | |
| Laccase from Trametes versicolor | powder, light brown, ?0.5 U/mg. Group: Fluorescence/luminescence spectroscopy. | |
| Laccase, Microorganisms | Laccase, Microorganisms (Denilite IIS) is a multi-copper oxidase (MCOs), which widely exists in microorganisms, plants and fungi, and can catalyze the oxidation of one electron of various phenolic compounds. Laccase can promote the oxidative coupling of single lignin, which plays an important role in the formation and biodegradation of lignin, and also has the potential to cross-link food polymers [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Denilite IIS. CAS No. 80498-15-3. Pack Sizes: 100 mg; 500 mg; 1 g. Product ID: HY-P2890. |  |
| LacDiNAc dimer ethylazide | LacDiNAc dimer ethylazide is a biomedical product used in the research of certain diseases or conditions related to carbohydrate recognition. It acts as a specific and potent inhibitor for various carbohydrate-binding proteins. Its structure and activity can be explored further at the provided websites, enabling potential therapeutic applications in drug discovery and development within the biomedical industry. Synonyms: GalNAcb(1-4)GlcNAcb(1-3)GalNAcb(1-4)GlcNAc-b-ethylazide. Molecular formula: C34H57N7O21. Mole weight: 899.85. | |
| L-Acetylcarnitine | L-Acetylcarnitine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nicetile, O-acetylcarnitine, R-Acetylcarnitine, acetylcarnitine, Acetyl-L-carnitine, Levocarnitine acetyl, L-O-Acetylcarnitine, (R)-Acetylcarnitine, (-)-Acetylcarnitine, O-Acetyl-L-carnitine, ALCAR, L-ACETYLCARNITINE, (-)O-acetylcarnitine, L-Carnitine acetyl ester, Acetyl-L-(-)-carnitine, Acetylcarnitine, (R)-Isomer, C9H18NO4, LS-17076, Ammonium, (3-carboxy-2-hydroxypropyl)trimethyl-, hydroxide, inner salt, acetate, L-, 1-Propanaminium, 2-(acetyloxy)-3-carboxy-N,N,N-trimethyl-, inner salt. Product Category: Heterocyclic Organic Compound. CAS No. 3040-38-8. Molecular formula: C9H17NO4. Mole weight: 203.24. Purity: 0.96. IUPACName: (3S)-3-acetyloxy-4-(trimethylazaniumyl)butanoate. Canonical SMILES: CC(=O)OC(CC(=O)[O-])C[N+](C)(C)C. ECNumber: 608-476-7. Product ID: ACM3040388. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lachnone A | It is a chromone isolated from the filamentous fungus, lachnum sp. It possesses weak activity against bacteria but has not been extensively investigated. Synonyms: Lanchnone A; 3,?5-Dihydroxy-2,?7-dimethyl-4H-1-benzopyran-4-one. Grades: >95% by HPLC. CAS No. 903892-99-9. Molecular formula: C11H10O4. Mole weight: 206.19. | |
| Lachnumol A | It is produced by the strain of Lachnum papyraceum. It has weaker activity against bacteria, yeast and filamentous fungi. It has cytotoxic activity against L1210, HeLa, KB and other cell lines. Synonyms: La; 1-chloro-6-[(Z)-1-chloroprop-1-enyl]-4-methoxy-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol; 7-Oxabicyclo(4.1.0)hept-3-ene-2,5-diol, 6-chloro-1-(1-chloro-1-propenyl)-3-methoxy-. CAS No. 150671-03-7. Molecular formula: C10H12Cl2O4. Mole weight: 267.11. | |
| Lachnumon | It is produced by the strain of Lachnum papyraceum. It has weaker activity against bacteria, yeast and filamentous fungi. It has cytotoxic activity against L1210, HeLa, KB and other cell lines. Synonyms: Ln; 7-Oxabicyclo(4.1.0)hept-3-en-2-one, 1-chloro-6-(1-chloro-1-propenyl)-5-hydroxy-4-methoxy-; 6-chloro-1-[(Z)-1-chloroprop-1-enyl]-2-hydroxy-3-methoxy-7-oxabicyclo[4.1.0]hept-3-en-5-one. CAS No. 150671-02-6. Molecular formula: C10H10Cl2O4. Mole weight: 265.09. | |
| Lacidipine | Lacidipine is an orally active and highly selective L-type calcium channel blocker that acts on smooth muscle calcium channels, primarily dilates peripheral arteries, reduces peripheral resistance, and has long-lasting anti-hypertensive activity. Lacidipine protects HKCs from apoptosis induced by ATP depletion and recovery by modulating the caspase-3 pathway. Lacidipine can be used in studies of hypertension, atherosclerosis and acute kidney injury (AKI). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3,5-pyridinedicarboxylicacid,1,4-dihydro-2,6-dimethyl-4-(2-(3-(1,1-dimethylet;diethylester,(e)-hoxy)-3-oxo-1-propenyl)phenyl);MOTENS;GX-1048;GR-43659X;CALDINE;(E)-4-[2-[3-(1,1-DIMETHYLETHOXY)-3-OXO-1-PROPENYL]PHENYL]-1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID DIETHYL ESTER;LACIPIL. Product Category: Inhibitors. Appearance: Solid. CAS No. 103890-78-4. Molecular formula: C26H33NO6. Mole weight: 455.54. Purity: 0.9979. Canonical SMILES: O=C(C1=C(C)NC(C)=C(C(OCC)=O)C1C2=CC=CC=C2/C=C/C(OC(C)(C)C)=O)OCC. Product ID: ACM103890784. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lacidipine | Lacidipine. Group: Biochemicals. Alternative Names: (E)-4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester, GR-43659X, GX-1048, caldine, lacipil, lacirex, motens. Grades: Highly Purified. CAS No. 103890-78-4. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C26H33NO6. US Biological Life Sciences. |  Worldwide |
| Lacidipine | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyapi standardsbritish pharmacopoeiapharmaceutical toxicologypharmacopoeial standards. Alternative Names: (E)-4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester, GR 43659X, Lacipil, GX 1048,Lacidipine, 4-[2-[(1E)-3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester, Lacirex, Caldine, Motens, Lacimen, Midotens. | |
| Lacidipine | Lacidipine (Lacipil, Motens) is a L-type calcium channel blocker. Lacidipine (Lacipil, Motens) works by relaxing and opening up the blood vessels. Synonyms: GX-1048,GR-43659X,SN-305; GX 1048,GR 43659X,SN 305; GX1048,GR43659X,SN305. Grades: >98%. CAS No. 103890-78-4. Molecular formula: C26H33NO6. Mole weight: 455.54. | |
| Lacidipine | Lacidipine is an orally active and highly selective L-type calcium channel blocker that acts on smooth muscle calcium channels, primarily dilates peripheral arteries, reduces peripheral resistance, and has long-lasting anti-hypertensive activity. Lacidipine protects HKCs from apoptosis induced by ATP depletion and recovery by modulating the caspase-3 pathway. Lacidipine can be used in studies of hypertension, atherosclerosis and acute kidney injury (AKI) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 103890-78-4. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-B0347. | |
| Lacidipine BP Impurity C | Lacidipine BP Impurity C. Uses: For analytical and research use. Group: Impurity standards. CAS No. 103890-79-5. Molecular formula: C26H33NO6. Mole weight: 455.55. Catalog: APB103890795. | |
| Lacidipine-d10 | A dihydropyridine calcium channel blocker. Antihypertensive. Group: Biochemicals. Alternative Names: (E)-4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Diethyl Ester-d10; GR-43659X-d10; GX-1048-d10; Caldine-d10; Lacipil-d10; Lacirex-d10; Motens-d10. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Lacidipine ((E)-4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Diethyl Ester, GR-43659X, GX-1048, Caldine, Lacipil, Lacirex, Motens) | A dihydropyridine calcium channel blocker. Group: Biochemicals. Alternative Names: (E)-4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Diethyl Ester, GR-43659X, GX-1048, Caldine, Lacipil, Lacirex, Motens. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Lacidipine Monomethyl Ester | an impurity of Lacidipine. Synonyms: 4-[2-[3-(1,1-Dimethylethoxy)-3-oxo-1-propenyl]phenyl]-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid Ethyl Methyl Ester. Grades: > 95%. CAS No. 103890-81-9. Molecular formula: C25H31NO6. Mole weight: 441.53. | |
| Lacinilene C | Lacinilene C. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Lacinilene C. Appearance: Yellow powder. CAS No. 41653-72-9. Molecular formula: C15H18O3. Mole weight: 246.3. Purity: 0.98. IUPACName: (1R)-1,7-dihydroxy-1,6-dimethyl-4-propan-2-ylnaphthalen-2-one. Canonical SMILES: CC1=C(C=C2C(=C1)C(=CC(=O)C2(C)O)C(C)C)O. Density: 1.194g/cm³. Product ID: ACM41653729. Alfa Chemistry ISO 9001:2015 Certified. | |
| LacK free acid | LacK (free acid) is a lysine derivative used in lactate acylation studies [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1227379-69-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W883690. | |
| Lacmoid | Lacmoid. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Lacnotuzumab | Lacnotuzumab (MCS110) is a neutralizing humanized IgG1/κ monoclonal antibody targeting CSF-1 that prevents CSF-1 from activating the CSF-1R. Lacnotuzumab can be used for the research of pigmented villonodular synovitis [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MCS110. CAS No. 1831128-32-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99368. | |
| Lacoferricin | HGAPDH is a synthetic antibacterial peptide. Synonyms: Ile-Glu-Gly-Arg-Phe-Lys-Cys-Arg-Arg-Trp-Gln-Trp-Arg-Met-Lys-Lys-Leu-Gly-Ala-Pro-Ser-Ile-Thr-Cys-Val-Arg-Arg-Ala-Phe. Grades: 96.7%. | |
| Lacolene | Lacolene. Category ALIPHATIC SOLVENTS. Pack Sizes Bulk/ Drums |  |
| Lacosamide | 100mg Pack Size. Group: Bioactive Small Molecules, Building Blocks, Organics, Research Organics & Inorganics. Formula: C13H18N2O3. CAS No. 175481-36-4. Prepack ID 17849212-100mg. Molecular Weight 250.29. See USA prepack pricing. |  |
| Lacosamide-13C, D3 solution | 1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Lacosamide-13C, D3 solution | 100 ?g/mL in acetonitrile, ampule of 1 mL, certified reference material. Group: Certified reference materials (crms). | |
| Lacosamide EP Impurity I | One of the impurities of Lacosamide. Lacosamide is a medication used for the adjunctive treatment of partial-onset seizures and diabetic neuropathic pain. Synonyms: (R)-N-Benzyl-2-(3-benzylureido)-3-methoxypropanamide. CAS No. 2295925-90-3. Molecular formula: C19H23N3O3. Mole weight: 341.40. | |
| Lacosamide Impurity 11 | Lacosamide Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1695551-74-6. Molecular formula: C13H18N2O3. Mole weight: 250.3. Catalog: APB1695551746. | |
| Lacosamide Impurity I | Cas No. 2295925-90-3. | |
| Lacosamide Liposome | Lacosamide is a NMDA receptor antagonist that acts on the glycine site and exhibits antiepileptic activity. This product is a pre-formulated liposome with lacosamide. It is only for research purposes. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes. |  |
| Lacosamide Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lacosamide Related Compound D | Lacosamide Related Compound D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1325220-61-8. Molecular formula: C13H18N2O6. Mole weight: 298.3. Catalog: APB1325220618. | |
| Lacosamide Related Compound D | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lacosamide Related Compound F | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lacquer Cellulose Nitrate Brushing Clear Grade 1:1 D/S 80-127/1 | 1lt Pack Size. Group: Building Blocks, Carbohydrates, Organics. Prepack ID 90023331-1lt. See USA prepack pricing. | |
| Lacquer Diluent | Lacquer Diluent. Category ALIPHATIC SOLVENTS. Pack Sizes Bulk/ Drums | |
| Lactacin F | Lactacin F is an antibacterial peptide isolated from Lactobacillus johnsonii VPI11088 (Laf+). It has activity against gram-positive bacteria. Synonyms: Asn-Arg-Trp-Gly-Asp-Thr-Val-Leu-Ser-Ala-Ala-Ser-Gly-Ala-Gly-Thr-Gly-Ile-Lys-Ala-Cys-Lys-Ser-Phe-Gly-Pro-Trp-Gly-Met-Ala-Ile-Cys-Gly-Val-Gly-Gly-Ala-Ala-Ile-Gly-Gly-Tyr-Phe-Gly-Tyr-Thr-His-Asn. CAS No. 107950-55-0. | |
| Lactacystin | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lactacystin | Cell-permeable. A potent and selective inhibitor of the 20S proteasome. Binds irreversibly to the active site N-terminal threonine residue of the catalytic beta-subunit of the 20S proteasome, thereby inhibiting its chymotrypsin and trypsin- like activities. Induces neurite outgrowth in Neuro 2A neuroblastoma cells and has been reported to induce apoptosis in human monoblast U937 cells. Also inhibits NF-kB activation (IC50 = 10uM). Group: Biochemicals. Grades: Highly Purified. CAS No. 133343-34-7. Pack Sizes: 200ug. US Biological Life Sciences. | Worldwide |
| Lactacystin | Lactacystin is a microbial metabolite isolated from streptomyces. It is a 20S proteasome inhibitor. Synonyms: (2R,3S,4R)-3-Hydroxy-2-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-5-oxo-2-pyrrolidinecarboxy-N-acetyl-L-cysteine thioester. Grades: ≥95%. CAS No. 133343-34-7. Molecular formula: C15H24N2O7S. Mole weight: 376.42. | |
| Lactacystin, Synthetic - CAS 1258004-00-0 | Lactacystin, Synthetic, CAS 1258004-00-0, is an irreversible inhibitor of 20S proteasome inhibitor (IC?? = 500 nM). A covalent inhibitor of the chymotrypsin & trypsin-like activities of proteasome. Group: Fluorescence/luminescence spectroscopy. | |
| Lactalbumin | 100g Pack Size. Group: Biochemicals, Diagnostic Raw Materials. Formula: N/A. CAS No. 9013-90-5. Prepack ID 10760053-100g. See USA prepack pricing. | |
| Lactalbumin | 500g Pack Size. Group: Biochemicals, Diagnostic Raw Materials. Formula: N/A. CAS No. 9013-90-5. Prepack ID 10760053-500g. See USA prepack pricing. | |
| Lactalbumin enzymatic hydrolysate | a mixture of soluble peptides and amino acids. Group: Fluorescence/luminescence spectroscopy. | |
| lactaldehyde dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (S)-lactaldehyde:NAD+ oxidoreductase. Other names in common use include L-lactaldehyde:NAD+ oxidoreductase, and nicotinamide adenine dinucleotide (NAD+)-linked dehydrogenase. This enzyme participates in pyruvate metabolism. Group: Enzymes. Synonyms: L-lactaldehyde:NAD oxidoreductase; nicotinamide adenine dinucleotide (NAD)-linked dehydrogenase. Enzyme Commission Number: EC 1.2.1.22. CAS No. 37250-90-1. Lactaldehyde dehydrogenase. 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-1128; lactaldehyde dehydrogenase; EC 1.2.1.22; 37250-90-1; L-lactaldehyde:NAD oxidoreductase; nicotinamide adenine dinucleotide (NAD)-linked dehydrogenase. Cat No: EXWM-1128. | |
| Lactaldehyde dehydrogenase from Escherichia coli, Recombinant | In enzymology, a lactaldehyde dehydrogenase (EC 1.2.1.22) is an enzyme that catalyzes the chemical reaction: (S)-lactaldehyde + NAD+ + H2O <-> (S)-lactate + NADH + 2 H+. The 3 substrates of this enzyme are (S)-lactaldehyde, NAD+, and H2O, whereas its 3 products are (S)-lactate, NADH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: E.C. 1.2.1.22; lactaldehyde dehydrogenase; L-lactaldehyde:NAD oxidoreductase; nicotinamide adenine dinucleotide (NAD)-linked dehydrogenase; (S)-lactaldehyde:NAD+ oxidoreductase. Enzyme Commission Number: EC 1.2.1.22. CAS No. 37250-90-1. Lactaldehyde dehydrogenase. Mole weight: 53337.9 Da. Source: Escherichia coli. E.C. 1.2.1.22; lactaldehyde dehydrogenase; L-lactaldehyde:NAD oxidoreductase; nicotinamide adenine dinucleotide (NAD)-linked dehydrogenase; (S)-lactaldehyde:NAD+ oxidoreductase. Cat No: NATE-1213. | |
| lactaldehyde reductase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (R)[or (S)]-propane-1,2-diol:NAD+ oxidoreductase. Other names in common use include propanediol:nicotinamide adenine dinucleotide (NAD+) oxidoreductase, and L-lactaldehyde:propanediol oxidoreductase. This enzyme participates in pyruvate metabolism and glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: propanediol:nicotinamide adenine dinucleotide (NAD) oxidoreductase; L-lactaldehyde:propanediol oxidoreductase. Enzyme Commission Number: EC 1.1.1.77. CAS No. 37250-15-0. 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-0360; lactaldehyde reductase; EC 1.1.1.77; 37250-15-0; propanediol:nicotinamide adenine dinucleotide (NAD) oxidoreductase; L-lactaldehyde:propanediol oxidoreductase. Cat No: EXWM-0360. | |
| lactaldehyde reductase (NADPH) | May be identical with EC 1.1.1.2 alcohol dehydrogenase (NADP+). Group: Enzymes. Synonyms: lactaldehyde (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADP-1,2-propanediol dehydrogenase; propanediol dehydrogenase; 1,2-propanediol:NADP+ oxidoreductase; lactaldehyde reductase (NADPH2). Enzyme Commission Number: EC 1.1.1.55. CAS No. 9028-43-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0340; lactaldehyde reductase (NADPH); EC 1.1.1.55; 9028-43-7; lactaldehyde (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADP-1,2-propanediol dehydrogenase; propanediol dehydrogenase; 1,2-propanediol:NADP+ oxidoreductase; lactaldehyde reductase (NADPH2). Cat No: EXWM-0340. | |
| Lactamase (Crude Enzyme) | Penicillinase from Bacillus cereushas been shown to contain three distinct species when purified and examined for homogeneity by sedimentation analysis, amino-terminal analysis, and vertical acrylamide gel electrophoresis. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; medicine; biotechnology; pharmacology. Group: Enzymes. Synonyms: penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase. Pack: 100ml. Cat No: NATE-1839. | |
| Lactaroviolin | It is produced by the strain of Lactarius deliciosus. It is an aromatic derivative antibiotic. It can inhibit the growth of Mycobacterium tuberculosis, but the effect is not strong. Synonyms: Lactarioviolin; 1-Azulenecarboxaldehyde, 4-methyl-7-(1-methylethenyl)-; 1-Formyl-7-isopropenyl-4-methylazulene; 1,3,5,7,9,11-Guaiahexaen-15-al; 7-Isopropenyl-4-methyl-1-Azulenecarboxaldehyde. CAS No. 85-33-6. Molecular formula: C15H14O. Mole weight: 210.27. | |
| lactase | The enzyme from intestinal mucosa is isolated as a complex that also catalyses the reaction of EC 3.2.1.62 glycosylceramidase. cf. EC 3.2.1.33 amylo-α-1,6-glucosidase. Group: Enzymes. Synonyms: lactase-phlorizin hydrolase. Enzyme Commission Number: EC 3.2.1.108. CAS No. 9031-11-2. 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-3791; lactase; EC 3.2.1.108; 9031-11-2; lactase-phlorizin hydrolase. Cat No: EXWM-3791. | |
| Lactase | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Lactase 100,000 ALU/g | Lactase 100,000 ALU/g. |  CA, FL & NJ |
| Lactate | Lactate (Lactic acid) is a hydroxycarboxylic acid receptor 1 (HCAR1) activator and an epigenetic modulator inducing lysine residues lactylation. Lactate is a glycolysis end-product, bridging the gap between glycolysis and oxidative phosphorylation. Lactate is an oncometabolite and has immune protective role of lactate in anti-tumor immunity [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Lactic acid. CAS No. 50-21-5. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B2227. | |
| lactate 2-monooxygenase | A flavoprotein (FMN). Group: Enzymes. Synonyms: lactate oxidative decarboxylase; lactate oxidase; lactic oxygenase; lactate oxygenase; lactic oxidase; L-lactate monooxygenase; lactate monooxygenase; L-lactate-2-monooxygenase. Enzyme Commission Number: EC 1.13.12.4. CAS No. 9028-72-2. Lactate oxidase. 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-0617; lactate 2-monooxygenase; EC 1.13.12.4; 9028-72-2; lactate oxidative decarboxylase; lactate oxidase; lactic oxygenase; lactate oxygenase; lactic oxidase; L-lactate monooxygenase; lactate monooxygenase; L-lactate-2-monooxygenase. Cat No: EXWM-0617. | |
| lactate aldolase | This enzyme belongs to the family of lyases, specifically the aldehyde-lyases, which cleave carbon-carbon bonds. This enzyme participates in pyruvate metabolism. Group: Enzymes. Synonyms: lactate synthase; (S)-lactate acetaldehyde-lyase. Enzyme Commission Number: EC 4.1.2.36. CAS No. 110777-33-8. 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-4873; lactate aldolase; EC 4.1.2.36; 110777-33-8; lactate synthase; (S)-lactate acetaldehyde-lyase. Cat No: EXWM-4873. | |
| Lactate calcium | Lactate (Lactic acid) calcium is used by the beverage industry as a source of calcium to fortify fruit juice. Lactate calcium facilitates the growth and phytic acid degradation of soybean sprouts [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lactic acid calcium. CAS No. 814-80-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B2227A. | |
| Lactate-d3 (sodium) (60% in water) | Lactate-d 3 sodium (60% in water) is the deuterium labeled Lactate sodium (60% in water). Lactate sodium (60% in water) is the product of glycogenolysis and glycolysis. Lactate sodium (60% in water) functions in a variety of biochemical processes [1] [2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Lactic acid-d3 sodium. CAS No. 1219802-24-0. Pack Sizes: 1 mg (5.20 M * 1.67 μL in Water); 5 mg (5.20 M * 8.36 μL in Water); 10 mg (5.20 M * 16.71 μL in Water). Product ID: HY-B2227BS1. | |
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