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Product
lipopolysaccharide glucosyltransferase II Transfers glucosyl residues to the D-galactosyl-D-glucosyl side-chains in the partially completed core of lipopolysaccharides. cf. EC 2.4.1.44 (lipopolysaccharide 3-α-galactosyltransferase), EC 2.4.1.56 (lipopolysaccharide N-acetylglucosaminyltransferase) and EC 2.4.1.58 (lipopolysaccharide glucosyltransferase I). Group: Enzymes. Synonyms: uridine diphosphoglucose-galactosylpolysaccharide glucosyltransferase. Enzyme Commission Number: EC 2.4.1.73. CAS No. 51004-27-4. 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-2616; lipopolysaccharide glucosyltransferase II; EC 2.4.1.73; 51004-27-4; uridine diphosphoglucose-galactosylpolysaccharide glucosyltransferase. Cat No: EXWM-2616. Creative Enzymes
lipopolysaccharide N-acetylglucosaminyltransferase Transfers N-acetylglucosaminyl residues to a D-galactose residue in the partially completed lipopolysaccharide core [cf. EC 2.4.1.44 (lipopolysaccharide 3-α-galactosyltransferase), EC 2.4.1.58 (lipopolysaccharide glucosyltransferase I) and EC 2.4.1.73 (lipopolysaccharide glucosyltransferase II)]. Group: Enzymes. Synonyms: UDP-N-acetylglucosamine-lipopolysaccharide N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-lipopolysaccharide acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:lipopolysaccharide N-acetyl-D-glucosaminyltransferase. Enzyme Commission Number: EC 2.4.1.56. CAS No. 37277-64-8. 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-2601; lipopolysaccharide N-acetylglucosaminyltransferase; EC 2.4.1.56; 37277-64-8; UDP-N-acetylglucosamine-lipopolysaccharide N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-lipopolysaccharide acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:lipopolysaccharide N-acetyl-D-glucosaminyltransferase. Cat No: EXWM-2601. Creative Enzymes
lipopolysaccharide N-acetylmannosaminouronosyltransferase Involved in the biosynthesis of common antigen in Enterobacteriaceae. Group: Enzymes. Synonyms: ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Enzyme Commission Number: EC 2.4.1.180. CAS No. 113478-30-1. 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-2406; lipopolysaccharide N-acetyl mannosaminouronosyl transferase; EC 2.4.1.180; 113478-30-1; ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Cat No: EXWM-2406. Creative Enzymes
Lipopolysaccharides Lipopolysaccharides Inhibitor. Uses: Scientific use. Product Category: T11855. CAS No.: TARGETMOL CHEMICALS
Lipopolysaccharides from Escherichia coli Lipopolysaccharides produced by Escherichia coli are endotoxins. Synonyms: Lipopolysaccharide E. Coli; Escherichia coli lipopolysaccharides; Lipopolysaccharides, Escherichiacoli; Citopyros; Escherichia coli lipopolysaccharide; Lipopolysaccharide, Escherichia coli; Lipopolysaccharides, Escherichia coli. CAS No. 93572-42-0. BOC Sciences 12
Lipopolysaccharides from Escherichia coli K-235 Lipopolysaccharides from Escherichia coli K-235. Alfa Chemistry Materials 3
Lipopolysaccharides from Escherichia coli O111:B4 Lipopolysaccharides from Escherichia coli O111:B4. Alfa Chemistry Materials 3
Lipopolysaccharides from Escherichia coli O127:B8 Lipopolysaccharides from Escherichia coli O127:B8. Alfa Chemistry Materials 3
Lipopolysaccharides from Escherichia coli O128:B12 Lipopolysaccharides from Escherichia coli O128:B12. Alfa Chemistry Materials 3
Lipopolysaccharides from Escherichia coli O26:B6 Lipopolysaccharides from Escherichia coli O26:B6. Alfa Chemistry Materials 3
Lipopolysaccharides from Escherichia coli O55:B5 Lipopolysaccharides from Escherichia coli O55:B5. Alfa Chemistry Materials 3
Lipopolysaccharides from Klebsiella pneumoniae Lipopolysaccharides from Klebsiella pneumoniae. Alfa Chemistry Materials 3
Lipopolysaccharides from Proteus mirabilis Lipopolysaccharides from Proteus mirabilis. Alfa Chemistry Materials 3
Lipopolysaccharides from Proteus vulgaris Lipopolysaccharides from Proteus vulgaris. Alfa Chemistry Materials 3
Lipopolysaccharides from Pseudomonas aeruginosa 10 Lipopolysaccharides from Pseudomonas aeruginosa 10. Alfa Chemistry Materials 3
Lipopolysaccharides from Salmonella enterica serotype abortus equi Lipopolysaccharides from Salmonella enterica serotype abortus equi. Alfa Chemistry Materials 3
Lipopolysaccharides from Salmonella enterica serotype enteritidis Lipopolysaccharides from Salmonella enterica serotype enteritidis. Alfa Chemistry Materials 3
Lipopolysaccharides from Salmonella enterica serotype minnesota Lipopolysaccharides from Salmonella enterica serotype minnesota. Alfa Chemistry Materials 3
Lipopolysaccharides from Salmonella enterica serotype typhimurium Lipopolysaccharides from Salmonella enterica serotype typhimurium. Alfa Chemistry Materials 3
Lipopolysaccharides from Salmonella typhosa Lipopolysaccharides from Salmonella typhosa. Alfa Chemistry Materials 3
Lipopolysaccharides from Serratia marcescens Lipopolysaccharides from Serratia marcescens. Alfa Chemistry Materials 3
Lipopolysaccharides (LPS) Lipopolysaccharides (LPSs, Endotoxin,LPS) is an endotoxin derived from the outer leaflet of the outer membrane of Gram-negative bacteria. Lipopolysaccharides consists of an antigen O-specific chain, a core oligosaccharide and lipid A. Lipopolysaccharides is a pathogenic associated molecular pattern (PAMP) that activates the immune system. Lipopolysaccharides activates TLR-4 on immune cells. Lipopolysaccharides induces secretion of cell migrasome. Group: Inhibitors. Alternative Names: LPSs, Endotoxin,LPS. CAS No. 93572-42-0. Pack Sizes: 1mg. Product ID: S7850. Storage Conditions: 3 years -20°C powder. Selleck Chemicals
United States; Europe
Lipopolysaccharides (rough strains) from Escherichia coli EH100 (Ra mutant) Lipopolysaccharides (rough strains) from Escherichia coli EH100 (Ra mutant). Alfa Chemistry Materials 3
Lipopolysaccharides (rough strains) from Escherichia coli F583 (Rd mutant) Lipopolysaccharides (rough strains) from Escherichia coli F583 (Rd mutant). Alfa Chemistry Materials 3
Lipopolysaccharides (rough strains) from Escherichia coli J5 (Rc mutant) Lipopolysaccharides (rough strains) from Escherichia coli J5 (Rc mutant). Alfa Chemistry Materials 3
Lipopolysaccharides (rough strains) from Salmonella enterica serotype minnesota Re 595 (Re mutant) Lipopolysaccharides (rough strains) from Salmonella enterica serotype minnesota Re 595 (Re mutant). Alfa Chemistry Materials 3
Lipopolysaccharides (rough strains) from Salmonella enterica serotype typhimurium SL1181 Lipopolysaccharides (rough strains) from Salmonella enterica serotype typhimurium SL1181. Alfa Chemistry Materials 3
Lipopolysaccharides (rough strains) from Salmonella enterica serotype typhimurium TV119 (Ra mutant) Lipopolysaccharides (rough strains) from Salmonella enterica serotype typhimurium TV119 (Ra mutant). Alfa Chemistry Materials 3
lipopolysaccharide-transporting ATPase ABC-type (ATP-binding cassette-type) ATPase, characterized by the presence of two similar ATP-binding domains. Does not undergo phosphorylation during the transport process. Enzymes of Gram-negative bacteria that export lipo-oligosaccharides and lipopolysaccharides. Group: Enzymes. Enzyme Commission Number: EC 7.5.2.5 (Formerly EC 3.6.3.39). 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-4677; lipopolysaccharide-transporting ATPase; EC 3.6.3.39. Cat No: EXWM-4677. Creative Enzymes
lipoprotein cholesterol lipoprotein cholesterol. Product ID: ACMA00005179. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
LIPOPROTEIN-CHOLESTEROL CONC LIPOPROTEIN-CHOLESTEROL CONC. Product ID: ACMA00005172. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
LIPOPROTEIN-CHOLESTEROL CONCENTRATE LIPOPROTEIN-CHOLESTEROL CONCENTRATE. Product ID: ACMA00005143. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
lipoprotein cholesterol ester lipoprotein cholesterol ester. Product ID: ACMA00005170. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
lipoprotein lipase Hydrolyses triacylglycerols in chylomicrons and low-density lipoproteins. Also hydrolyses diacylglycerol. Group: Enzymes. Synonyms: clearing factor lipase; diglyceride lipase; diacylglycerol lipase; postheparin esterase; diglyceride lipase; postheparin lipase; diacylglycerol hydrolase; lipemia-clearing factor. Enzyme Commission Number: EC 3.1.1.34. CAS No. 9004-2-8. LPL. 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-3460; lipoprotein lipase; EC 3.1.1.34; 9004-02-8; clearing factor lipase; diglyceride lipase; diacylglycerol lipase; postheparin esterase; diglyceride lipase; postheparin lipase; diacylglycerol hydrolase; lipemia-clearing factor. Cat No: EXWM-3460. Creative Enzymes
Lipoprotein lipase Lipoprotein lipase. Uses: For analytical and research use. CAS No. 9004-2-8. Catalog: AP9004028-C. Alfa Chemistry Analytical Products
Lipoprotein Lipase from Burkholderia sp. Lipoprotein Lipase from Burkholderia sp. Uses: For analytical and research use. CAS No. 9004-2-8. EC Number: 232-669-1. Catalog: AP9004028-A. Alfa Chemistry Analytical Products
Lipoprotein Lipase from Pseudomonas sp. Lipoprotein Lipase from Pseudomonas sp. Uses: For analytical and research use. CAS No. 9004-2-8. EC Number: 232-669-1. Catalog: AP9004028-B. Alfa Chemistry Analytical Products
Lipoproteins, HDL Cholesterol Lipoproteins, HDL Cholesterol. Product ID: ACMA00005175. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
Lipoproteins, LDL Cholesterol Lipoproteins, LDL Cholesterol. Product ID: ACMA00005140. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
Lipoproteins, VLDL Cholesterol Lipoproteins, VLDL Cholesterol. Product ID: ACMA00005133. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
lipoprotein-X cholesterol lipoprotein-X cholesterol. Product ID: ACMA00005174. Alfa Chemistry - ISO 9001:32057 Certified. Alfa Chemistry. 2
Liposidolide A It is produced by the strain of Str. sp. RS-28. It's a macrolide antibiotic. It is resistant to plant pathogenic fungi and algae. Molecular formula: C78H138O30. Mole weight: 1555.91. BOC Sciences 12
Liposidomycin A It is produced by the strain of Str. sp. SN-1061M. It has antibacterial effect, but the antibacterial activity is weak. It has strong inhibition of mycobacteria (MIC is 0.16 μg/mL). It has the function of inhibiting glycopeptide biosynthesis, and can inhibit the glycopeptide biosynthesis of Escherichia coli with IC50 of 0.03 μg/mL. Molecular formula: C44H67N5O21S. Mole weight: 1034.09. BOC Sciences 12
Liposidomycin B It is produced by the strain of Str. sp. SN-1061M. It has antibacterial effect, but the antibacterial activity is weak. It has strong inhibition of mycobacteria (MIC is 0.16 μg/mL). It has the function of inhibiting glycopeptide biosynthesis, and can inhibit the glycopeptide biosynthesis of Escherichia coli with IC50 of 0.03 μg/mL. Molecular formula: C42H67N5O21S. Mole weight: 1010.06. BOC Sciences 12
Liposidomycin C It is produced by the strain of Str. sp. SN-1061M. It has antibacterial effect, but the antibacterial activity is weak. It has strong inhibition of mycobacteria (MIC is 0.16 μg/mL). It has the function of inhibiting glycopeptide biosynthesis, and can inhibit the glycopeptide biosynthesis of Escherichia coli with IC50 of 0.03 μg/mL. Molecular formula: C42H67N5O21S. Mole weight: 1010.06. BOC Sciences 12
Liposomal Iron Liposomal Iron. CAS No. 10058-44-3. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. Cenik Chemicals
Liposomal Iron bisglycinate Liposomal Iron bisglycinate. CAS No. 20150-34-9. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. Cenik Chemicals
Lipoteichoic acid Lipoteichoic acid is an orally effect anti-inflammatory and antitumor agent. Lipoteichoic acid is a crucial immune molecule in Gram-positive bacteria that activates the complement system by inducing C3 and inhibiting CD55. Lipoteichoic acid regulates macrophage autophagy through the PI3K/Akt/mTOR pathway. Lipoteichoic acid induces lung damage in mice. Lipoteichoic acid inhibits the production of melanin[1][2][3][4][5][6][7]. Uses: Scientific research. Category: Signaling pathways. CAS No. 56411-57-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N9481. MedChemExpress MCE
Lipoxamycin hemisulfate Lipoxamycin hemisulfate is an antifungal antibiotic and a potent serine palmitoyltransferase inhibitor with an IC50 of 21 nM[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 11075-87-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119759A. MedChemExpress MCE
Lipoxidase 100mg Pack Size. Group: Biochemicals, Research Organics & Inorganics. Formula: N/A. CAS No. 9029-60-1. Prepack ID 14946502-100mg. See USA prepack pricing. Molekula Americas
lipoyl amidotransferase In the bacterium Listeria monocytogenes the enzyme takes part in a pathway for scavenging of lipoic acid. The enzyme is bound to 2-oxo-acid dehydrogenases such as the pyruvate dehydrogenase complex, where it transfers the lipoyl moiety from lipoyl-[glycine cleavage system H] to the E2 subunits of the complexes. Group: Enzymes. Synonyms: LipL (gene name, ambiguous). Enzyme Commission Number: EC 2.3.1.200. 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-2145; lipoyl amidotransferase; EC 2.3.1.200; LipL (gene name, ambiguous). Cat No: EXWM-2145. Creative Enzymes
lipoyl(octanoyl) transferase This is the first committed step in the biosynthesis of lipoyl cofactor. Lipoylation is essential for the function of several key enzymes involved in oxidative metabolism, as it converts apoprotein into the biologically active holoprotein. Examples of such lipoylated proteins include pyruvate dehydrogenase (E2 domain), 2-oxoglutarate dehydrogenase (E2 domain), the branched-chain 2-oxoacid dehydrogenases and the glycine cleavage system (H protein). Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the true substrate. The other enzyme involved in the biosynthesis of lipoyl cofactor is EC 2.8.1.8, lipoyl synthase. An alternative lipoylation pathway invol.rase; octanoyl-[acyl-carrier-protein]:protein N-octanoyltransferase. Enzyme Commission Number: EC 2.3.1.181. CAS No. 392687-64-8. 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-2123; lipoyl(octanoyl) transferase; EC 2.3.1.181; 392687-64-8; LipB; lipoyl (octanoyl)-[acyl-carrier-protein]-protein N-lipoyltransferase; lipoyl (octanoyl)-acyl carrier protein:protein transferase; lipoate/octanoate transferase; lipoyltransferase; octanoyl-[acyl carrier protein]-protein N-octanoyltransferase; lipoyl(octanoyl)transferase; octanoyl-[acyl-carrier-protein]:protein N-octanoyltransferase. Cat No: EXWM-2123. Creative Enzymes
lipoyl synthase This enzyme is a member of the 'AdoMet radical' (radical SAM) family, all members of which produce the 5'-deoxyadenosin-5'-yl radical and methionine from AdoMet [i.e. S-adenosylmethionine, or S-(5'-deoxyadenosin-5'-yl)methionine], by the addition of an electron from an iron-sulfur centre. The radical is converted into 5'-deoxyadenosine when it abstracts a hydrogen atom from C-6 and C-8, leaving reactive radicals at these positions so that they can add sulfur, with inversion of configuration. This enzyme catalyses the final step in the de-novo biosynthesis of the lipoyl cofactor, with the other enzyme involved being EC 2.3.1.181, lipoyl(octanoyl) transferase. Lipoylation is essential.pathway involves EC 2.7.7.63, lipoate-protein ligase, which can lipoylate apoproteins using exogenous lipoic acid (or its analogues). Group: Enzymes. Synonyms: LS; LipA; lipoate synthase; protein 6-N-(octanoyl)lysine:sulfur sulfurtransferase; protein N6-(octanoyl)lysine:sulfur sulfurtransferase. Enzyme Commission Number: EC 2.8.1.8. CAS No. 189398-80-9. 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-3366; lipoyl synthase; EC 2.8.1.8; 189398-80-9; LS; LipA; lipoate synthase; protein 6-N-(octanoyl)lysine:sulfur sulfurtransferase; protein N6-(octanoyl)lysine:sulfur sulfurtransferase. Cat No: EXWM-3366. Creative Enzymes
Liproxstatin-1 Liproxstatin-1 is a potent ferroptosis inhibitor and inhibits ferroptotic cell death (IC50=22 nM)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 950455-15-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-12726. MedChemExpress MCE
Liproxstatin-1 Liproxstatin-1 is a potent ferroptosis inhibitor with an IC50 of 22 nM. Group: Inhibitors. CAS No. 950455-15-9. Pack Sizes: 5mg. Product ID: S7699. Formula: C19H21ClN4. Smiles: C1CNCCC12C(=NCC3=CC(=CC=C3)Cl)NC4=CC=CC=C4N2. Storage Conditions: 2 years -80 in solvent. Selleck Chemicals
United States; Europe
Liproxstatin-1 Liproxstatin-1 Inhibitor. Uses: Scientific use. Product Category: T2376. CAS No. 950455-15-9. TARGETMOL CHEMICALS
Liproxstatin-1 hydrochloride Liproxstatin-1 hydrochloride is a potent ferroptosis inhibitor and inhibits ferroptotic cell death (IC50=22 nM)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2250025-95-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12726A. MedChemExpress MCE
Lipstatin Lipstatin, a potent inhibitor of the pancreas lipase, is reported to be useful in the treatment and/or prevention of obesity and related diseases. Group: Biochemicals. Alternative Names: N-Formyl-L-leucine (1S,3Z,6Z)-1-[[(2S,3S)-3-Hexyl-4-oxo-2-oxetanyl]methyl]-3,6-dodecadien-1-yl Ester; N-Formyl-L-leucine [2S-[2α(1R*,3Z,6Z),3 β]]-. Grades: Highly Purified. CAS No. 96829-59-3. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 11
Worldwide
Lipstatin Lipstatin, a potent inhibitor of the pancreas lipase, is reported to be useful in the treatment and prevention of obesity and related diseases. It is a natural product that was first isolated from Actinobacterium Streptomyces toxytricini. Synonyms: N-Formyl-L-leucine (1S,3Z,6Z)-1-[[(2S,3S)-3-Hexyl-4-oxo-2-oxetanyl]methyl]-3,6-dodecadien-1-yl Ester; N-Formyl-L-leucine [2S-[2α(1R*,3Z,6Z),3β]]-1-[(3-Hexyl-4-oxo-2-oxetanyl)methyl]-3,6-dodecadienyl Ester; (-)-Lipstatin. Grade: >95%. CAS No. 96829-59-3. Molecular formula: C29H49NO5. Mole weight: 491.70. BOC Sciences
Liq Electron transport and hole blocking material in organic light emitting diodes (OLED). Alternative Names: (8-Hydroxyquinolinato)lithium,(8-Quinolinolato)lithium,8-Hydroxyquinoline lithium. CAS No. 25387-93-3. Molecular formula: C9H6LiNO. Mole weight: 151.09. IUPAC Name: lithium;quinolin-8-olate. SMILES: [Li+].C1=CC2=C(C(=C1)[O-])N=CC=C2. InChI: 1S/C9H7NO.Li/c11-8-5-1-3-7-4-2-6-10-9(7)8;/h1-6,11H;/q;+1/p-1,FQHFBFXXYOQXMN-UHFFFAOYSA-M. Alfa Chemistry Materials 5
Liq; Lithium 8-Hydroxyquinolinolate, >99% (HPLC), Sublimed Liq; Lithium 8-Hydroxyquinolinolate, >99% (HPLC), Sublimed. CAS No. 850918-68-2. Molecular formula: C9H6LiNO. Mole weight: 151.1g/mol. IUPAC Name: lithium;quinolin-8-olate. SMILES: [Li+].C1=CC2=C(C(=C1)[O-])N=CC=C2. InChI: InChI=1S/C9H7NO.Li/c11-8-5-1-3-7-4-2-6-10-9(7)8;/h1-6,11H;/q;+1/p-1. Alfa Chemistry Materials 5
Liquefied CNT Paste Liquefied CNT Paste. CAS No. 308068-56-6. Molecular formula: C. Mole weight: 12.03g/mol. Purity: 99.99%. Alfa Chemistry Materials 7
Liquidambaric lactone Liquidambaric lactone. Group: Biochemicals. Alternative Names: 11,12-Epoxy-3-oxo-28,13-oleananolide. Grades: Plant Grade. CAS No. 185051-75-6. Pack Sizes: 10mg. Molecular Formula: C30H44O4, Molecular Weight: 468.668. US Biological Life Sciences. USBiological 11
Worldwide
Liquid Crystal, TK-LQ 2040, Electric effect type, Mesomorphic range:20-40deg C [Nematic Liquid Crystal] Liquid Crystal, TK-LQ 2040, Electric effect type, Mesomorphic range:20-40deg C [Nematic Liquid Crystal]. Alfa Chemistry Materials 4
Liquid Crystal, TK-LQ 3858, Electric effect type, Mesomorphic range:38-58deg C [Nematic Liquid Crystal] Liquid Crystal, TK-LQ 3858, Electric effect type, Mesomorphic range:38-58deg C [Nematic Liquid Crystal]. Alfa Chemistry Materials 4
Liquiritigenin Liquiritigenin, a flavanone isolated from Glycyrrhiza uralensis, is a highly selective estrogen receptor β (ERβ) agonist with an EC50 of 36.5 nM for activation of the ERE tk-Luc. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 4',7-Dihydroxyflavanone. CAS No. 578-86-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0377. MedChemExpress MCE
Liquiritigenin Liquiritigenin is a natural flavonoid compound found in the root of Glycyrrhiza uralensis Fisch. Liquiritigenin exhibits anti-inflammatory, antihyperlipidemic and antiallergic activities. Liquiritigenin is an estrogenic compound which acts as an agonist s. Synonyms: 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-, (2S)-; (2S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-, (S)-; Flavanone, 4',7-dihydroxy-; (-)-(2S)-7,4'-Dihydroxyflavanone; (-)-(S)-4',7-Dihydroxyflavanone; (-)-Liquiritigenin; (2S)-Liquiritigenin; 4',7-Dihydroxyflavanone; 7,4'-Dihydroxyflavanone; Menerba. Grade: >98%. CAS No. 578-86-9. Molecular formula: C15H12O4. Mole weight: 256.25. BOC Sciences 9
Liquiritigenin Liquiritigenin. Group: Biochemicals. Grades: Purified. CAS No. 578-86-9. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 11
Worldwide
Liquiritin Liquiritin. Group: Biochemicals. Alternative Names: Liquiritoside. Grades: Plant Grade. CAS No. 551-15-5. Pack Sizes: 20mg. Molecular Formula: C21H22O9, Molecular Weight: 418.394. US Biological Life Sciences. USBiological 11
Worldwide
Liquiritin Liquiritin is a natural flavonoid compound found in the root of Glycyrrhiza glabra L. Liquiritin shows potential antidepressant-like effection and can increase SOD activity, inhibit lipid peroxidation, and lessen production of MDA. Uses: Antidepressant. Synonyms: 4,7-Dihydroxyflavanone-4-(b-D-glucopyranoside); Likviritin; Liquiritoside. Grade: >98%. CAS No. 551-15-5. Molecular formula: C21H22O9. Mole weight: 418.39. BOC Sciences 9

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