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| Product | Description | |
|---|---|---|
| L-Tyrosine methyl ester | L-Tyrosine-induced antinociception is mediated by central delta-opioid receptors and by the bulbo-spinal noradrenergic system. Synonyms: L-Tyr-OMe; Methyl L-tyrosinate; Tyrosine methyl ester; Methyl tyrosinate; (S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester. Grade: ≥98%. CAS No. 1080-06-4. Molecular formula: C10H13NO3. Mole weight: 195.20. |  |
| L-Tyrosine Methyl Ester | L-Tyrosine Methyl Ester. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1080-06-4. IUPAC Name: methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate. Molecular formula: C10H13NO3. Mole weight: 195.22. Catalog: APS1080064. SMILES: COC(=O)[C@@H](N)Cc1ccc(O)cc1. Format: Neat. Shipping: Room Temperature. |  |
| L-Tyrosine methyl ester hydrochloride | L-Tyrosine methyl ester hydrochloride. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. |  Worldwide |
| L-Tyrosine methyl ester hydrochloride | L-Tyrosine methyl ester hydrochloride. Synonyms: L-Tyr-OMe HCl; H-L-TYR-OME HCl; L-Tyr-OMe hydrochloride; L-Tyrosinemethylesterhydrochloride; TYROSINE-OME HCl; L-Tyrosine Methyl ester HCl. Grade: ≥ 99.5% (HPLC, Chiral purity). CAS No. 3417-91-2. Molecular formula: C10H13NO3·HCl. Mole weight: 231.70. | |
| L-Tyrosine methyl ester hydrochloride 99+% | L-Tyrosine methyl ester hydrochloride 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| L-Tyrosine methyl ester (phenyl-13C6) hydrochloride | L-Tyrosine methyl ester (phenyl-13C6) hydrochloride. Uses: Peptide synthesis. Product Category: Amino Acids. CAS No. 857665-74-8. Molecular formula: HO13C6H4CH2CH(NH2)COOCH3 ?HCl. Mole weight: 237.63. Canonical SMILES: Cl.COC(=O)[C@@H](N)C[13c]1[13cH][13cH][13c](O)[13cH][13cH]1. Product ID: ACM857665748. Alfa Chemistry ISO 9001:2015 Certified. |  |
| L-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-,2,5-dioxo-1-pyrrolidinyl ester | L-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-,2,5-dioxo-1-pyrrolidinyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: NSC334308, CID333430, 20866-56-2. Product Category: Heterocyclic Organic Compound. CAS No. 20866-56-2. Molecular formula: C18H22N2O7. Mole weight: 378.38. Purity: 0.96. IUPACName: (2,5-dioxopyrrolidin-1-yl) 3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate. Canonical SMILES: CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)O)C(=O)ON2C(=O)CCC2=O. Density: 1.35g/cm³. Product ID: ACM20866562. Alfa Chemistry ISO 9001:2015 Certified. Categories: Boc-Tyr-OSu. | |
| L-Tyrosine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3,5-dinitro- | L-Tyrosine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3,5-dinitro-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-3,5-dinitro-L-tyrosine, CTK8E5921, 195434-42-5. Product Category: Heterocyclic Organic Compound. CAS No. 195434-42-5. Molecular formula: C24H19N3O9. Mole weight: 493.43. Purity: 0.96. IUPACName: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxy-3,5-dinitrophenyl)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=C(C(=C4)[N+](=O)[O-])O)[N+](=O)[O-])C(=O)O. Product ID: ACM195434425. Alfa Chemistry ISO 9001:2015 Certified. | |
| L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-O-2-propen-1-yl- | L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-O-2-propen-1-yl-. CAS No. 2306128-24-3. Molecular formula: C28H27NO5. Mole weight: 457.52. | |
| L-Tyrosine,N-acetyl-O-(1,1-dimethylethyl)- | L-Tyrosine,N-acetyl-O-(1,1-dimethylethyl)-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AC-TYR(TBU)-OH, 201292-99-1, MolPort-020-003-794, AK170221, K-5886. Product Category: Heterocyclic Organic Compound. CAS No. 201292-99-1. Molecular formula: C15H21NO4. Mole weight: 279.34. Purity: 0.95. IUPACName: (2S)-2-acetamido-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid. Canonical SMILES: CC(=O)NC(CC1=CC=C(C=C1)OC(C)(C)C)C(=O)O. Product ID: ACM201292991. Alfa Chemistry ISO 9001:2015 Certified. | |
| L-Tyrosine,N-acetyl-O-methyl-,methyl ester | L-Tyrosine,N-acetyl-O-methyl-,methyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Acetyl-O-methyl-L-tyrosine methyl ester, 17355-24-7, AC1OCUSF, SureCN5706152, CTK8B3444, ANW-42531, AKOS015910081, AG-E-23096, I14-31150, methyl (2S)-2-acetamido-3-(4-methoxyphenyl)propanoate, Alanine,N-acetyl-3-(p-methoxyphenyl)-, methyl ester (7CI); Alanine,N-acetyl-3-(p-methoxyphenyl)-, methyl ester, L- (8CI); (+)-Methyl(2S)-2-(Acetylamino)-3-(4-methoxyphenyl)propanoate; (S)-Methyl2-acetylamino-3-(4-methoxyphenyl)propanoate; N-Acetyl-4-methoxy-L-phenylalaninemethyl ester; N-Acetyl-L-4-methoxyphenylalanine methyl ester;N-Acetyl-L-O-methyltyrosine methyl ester. Product Category: Heterocyclic Organic Compound. CAS No. 17355-24-7. Molecular formula: C13H17NO4. Mole weight: 251.28. Purity: 0.96. IUPACName: methyl (2S)-2-acetamido-3-(4-methoxyphenyl)propanoate. Canonical SMILES: CC(=O)NC(CC1=CC=C(C=C1)OC)C(=O)OC. Product ID: ACM17355247. Alfa Chemistry ISO 9001:2015 Certified. Categories: Ac-tyr(me)-ome. | |
| L-Tyrosine (non-animal) | L-Tyrosine (non-animal). Group: Biochemicals. Alternative Names: (-)-α-Amino-p-hydroxyhydrocinnamic Acid; Therigon; p-Tyrosine; (2S) -2-Amino-3- (4-hydroxyphenyl) propanoic Acid; (S) -2-Amino-3- (4-hydroxyphenyl) propanoic Acid; (S)-Tyrosine; (S) - α -Amino-4-hydroxy Benzene propanoic Acid; L-(-)-Tyrosine; NSC 82624; NSC 9973`. Grades: Cell Culture Grade. CAS No. 60-18-4. Pack Sizes: 100g, 500g, 1Kg. Molecular Formula: C9H11NO3, Molecular Weight: 181.19. US Biological Life Sciences. | Worldwide |
| L-Tyrosine-N-T-BOC, O-BZ ether-[15N] | L-Tyrosine-N-T-BOC, O-BZ ether-[15N] is a 15N labelled analogue of Boc-Tyr(Bzl)-OH, which is an amino acid building block used in peptide synthesis. Synonyms: Boc-O-benzyl-L-tyrosine-15N; N-Boc-O-benzyl-L-tyrosine-15N; Boc-Tyr(Bzl)-OH-15N. Grade: 98% by CP; 98% atom 15N. Molecular formula: C21H25[15N]O5. Mole weight: 372.42. | |
| L-Tyrosine-N-T-Boc, O-Bz ether-[ring-d4] | L-Tyrosine-N-T-Boc, O-Bz ether-[ring-d4] is a labelled Boc-O-benzyl-L-tyrosine, which is a protected L-tyrosine. Tyrosine is a non-essential amino acid synthesized from phenylalanine. It is the precursor of some neurotransmitters. Synonyms: Boc-O-benzyl-L-tyrosine (ring-d4); N-Boc-O-benzyl-L-tyrosine (ring-d4); Boc-Tyr(Bzl)-OH (ring-d4). Grade: 98% by CP; 98% atom D. Molecular formula: C21H21D4NO5. Mole weight: 375.45. | |
| L-Tyrosine,o-(dimethoxyphosphinyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- | L-Tyrosine,o-(dimethoxyphosphinyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-Tyr(PO3Me2)-OH, Fmoc-O-(dimethylphospho)-L-tyrosine, SureCN8152459, 47523_ALDRICH, 47523_FLUKA, AKOS015909512, I14-32663, 127633-36-7. Product Category: Heterocyclic Organic Compound. CAS No. 127633-36-7. Molecular formula: C26H26NO8P. Mole weight: 511.46. Purity: 0.96. IUPACName: (2S)-3-(4-dimethoxyphosphoryloxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: COP(=O)(OC)OC1=CC=C(C=C1)CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24. Density: 1.343g/cm³. Product ID: ACM127633367. Alfa Chemistry ISO 9001:2015 Certified. | |
| L-Tyrosine-[phenol-17O] | L-Tyrosine-[phenol-17O], a 17O labelled analogue of L-Tyrosine. L-Tyrosine is biologically converted from L-phenylalanine and in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine. Grade: 98% by CP; 40% atom 17O. Molecular formula: C9H11NO2[17O]. Mole weight: 182.19. | |
| L-Tyrosine-[phenol-18O] | L-Tyrosine-[phenol-18O], a 18O labelled analogue of L-Tyrosine. L-Tyrosine is biologically converted from L-phenylalanine and in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine. Grade: 98% by CP; 90% atom 18O. Molecular formula: C9H11NO2[18O]. Mole weight: 183.19. | |
| L-Tyrosine-[phenol-3,5-13C2] | L-Tyrosine-[phenol-3,5-13C2] is a 13C labelled analogue of L-Tyrosine. L-Tyrosine is biologically converted from L-phenylalanine and in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine. Grade: 98% by CP; 99% atom 13C. Molecular formula: C7[13C]2H11NO3. Mole weight: 183.17. | |
| L-Tyrosine-[phenol-4-13C] | L-Tyrosine-[phenol-4-13C] is a 13C labelled analogue of L-Tyrosine. L-Tyrosine is a non-essential amino acid and one of the 22 amino acids used in the synthesis of protein. It is derived from phenylalanine in human body and abundant in high-protein food products. Grade: 98% by CP; 99% atom 13C. CAS No. 81201-90-3. Molecular formula: C8[13C]H11NO3. Mole weight: 182.18. | |
| L-Tyrosine-(phenyl-13C6) | 99 atom % 13C, 99% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| L-Tyrosine-(phenyl-3,5-d2) | 98 atom % D, 99% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| L-Tyrosine-[phenyl-3,5-d2] | L-Tyrosine-[phenyl-3,5-d2] is a labelled L-tyrosine. Tyrosine is a non-essential amino acid synthesized from phenylalanine. It is the precursor of some neurotransmitters. Synonyms: L-Tyrosine-d2; p-Hydroxyphenyl-L-alanine-d2; H-L-Tyr-OH-d2; L-Tyrosine-(phenyl-3,5-d2). Grade: 95% by HPLC; 98% atom D. CAS No. 30811-19-9. Molecular formula: C9H9D2NO3. Mole weight: 183.20. | |
| L-Tyrosine-(phenyl-d4) | ?98 atom % D, ?99% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| L-Tyrosine-[phenyl-d4] | L-Tyrosine-[phenyl-d4] is a labelled L-tyrosine. Tyrosine is a non-essential amino acid synthesized from phenylalanine. It is the precursor of some neurotransmitters. Synonyms: L-Tyrosine-d4; p-Hydroxyphenyl-L-alanine-d4; H-L-Tyr-OH-d4; L-4-Hydroxyphenyl-2,3,5,6-d4-alanine; L-Tyrosine-(phenyl-d4). Grade: 95% by HPLC; 98% atom D. CAS No. 62595-14-6. Molecular formula: C9H7D4NO3. Mole weight: 185.21. | |
| L-Tyrosine-[ring-13C6] | L-Tyrosine-[ring-13C6] is a 13C labelled analogue of L-Tyrosine. L-Tyrosine is a non-essential amino acid that can inhibit citrate synthase activity in the posterior cortex. Synonyms: L-Tyrosine (phenyl-13C6); H-Tyr-OH-13C6; (2S)-2-amino-3-(4-hydroxy(1,2,3,4,5,6-13C6)cyclohexa-1,3,5-trien-1-yl)propanoic acid; L-4-hydroxyphenyl-13C6-alanine. Grade: 98% by CP; 99% atom 13C. CAS No. 201595-63-3. Molecular formula: C3[13C]6H11NO3. Mole weight: 187.14. | |
| L-Tyrosine-[ring-d2,13C6] | L-Tyrosine-[ring-d2,13C6] is a 13C labelled analogue of L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. Synonyms: L-Tyrosine (Ring-13C6,3,3-d2). Grade: 98% by CP; 99% atom 13C; 30% atom D. CAS No. 420107-77-3. Molecular formula: C3[13C]6H9D2NO3. Mole weight: 189.16. | |
| L-Tyrosine (Standard) | L-Tyrosine (Standard) is the analytical standard of L-Tyrosine. This product is intended for research and analytical applications. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. Uses: Scientific research. Group: Natural products. CAS No. 60-18-4. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0473R. |  |
| L-Tyrosine tert-butyl ester | L-Tyrosine tert-butyl ester is a protected form of L-Tyrosine. L-Tyrosine is an essential amino acid that exhibits in vitro antioxidant and antiradical activities. L-Tyrosine is used as a precursor to synthesize catecholamines in human keratinocytes, and also for the synthesis of proteins and thyroid hormones. Synonyms: L-Tyr-OtBu; H-Tyr-OtBu; tert-Butyl L-tyrosinate; L-tyrosine-COOBu-t; L-Tyrosine tert-butyl ester; t-butyl ester of tyrosine. Grade: ≥ 99% (HPLC). CAS No. 16874-12-7. Molecular formula: C13H19NO3. Mole weight: 237.30. | |
| L-Tyrosine tert-butyl ester | L-Tyrosine tert-butyl ester. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| L-Tyrosinol | L-Tyrosinol. Synonyms: Tyrosinol; H-Tyrosinol; (S)-4-(2-Amino-3-hydroxypropyl)phenol; 4-[(2S)-2-amino-3-hydroxypropyl]phenol. CAS No. 5034-68-4. Molecular formula: C9H13NO2. Mole weight: 167.17. | |
| L-Tyrosinol hydrochloride 99+% (HPLC) | L-Tyrosinol hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| LU-002i | LU-002i is a subunit-selective human proteasome β2c and β2i inhibitor with an IC 50 value of 220 nM for β2i [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1838705-22-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-157034. | |
| LU-005i | LU-005i is a potent inhibitor of ?5i subunit of immunoproteasomes (IC50 = 6.6 nM), selective over ?5c subunit (IC50 = 287 nM)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1620107-33-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-148732. | |
| Lu AA33810 | Lu AA33810 is a potent and selective antagonist of neuropeptide Y5 receptor with a K i of 1.5 nM for the human receptor. Lu AA33810 exhibts antianxiolytic-like and antidepressant-like effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 304008-29-5. Pack Sizes: 1 mg. Product ID: HY-107729. | |
| LU AA33810 | LU AA33810. Group: Biochemicals. Grades: Purified. CAS No. 304008-29-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Lu AA 47070 | Lu AA 47070. Group: Biochemicals. Grades: Purified. CAS No. 913842-25-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Lubabegron | Lubabegron is a potent modulator of β-adrenergic receptor ( β -AR ). Lubabegron demonstrates antagonistic behavior at the β 1 and β? 2 receptor subtypes and agonistic behavior at the β? 3 receptor subtype in cattle. Lubabegron reduces NH 3 gas emissions from an animal or its waste [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY-488756. CAS No. 391920-32-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123012. | |
| Lubeluzole | Lubeluzole is a neuroprotective anti-ischemic compound. Lubeluzole, but not its (-)-R-isomer, protects against sensorimotor deficits provoked by photochemical stroke in rats. Lubeluzole inhibited glutamate-stimulated guanosine 3',5'-cyclic monophosphate production with an IC 50 of 37 nM. Lubeluzole also has the potential for developing a novel class of antibacterial adjuvants endowed with spasmolytic activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 144665-07-6. Pack Sizes: 5 mg. Product ID: HY-105084. | |
| Lubeluzole dihydrochloride | Lubeluzole (dihydrochloride) is a neuroprotective agent which blockades neuronal voltage-gated sodium channels. Lubeluzole (dihydrochloride) also produces both tonic and block of cardiac sodium channels. Lubeluzole (dihydrochloride) is promising for research of antiarrhythmic agents [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 144665-09-8. Pack Sizes: 1 mg. Product ID: HY-105084A. | |
| Lubeluzole dihydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lubiprostone | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopychiral molecules. Alternative Names: (11?)-16,16-difluoro-11-hydroxy-9,15-dioxo-Prostan-1-oic acid, Lubiprostone, Ru 0211. | |
| Lubiprostone | Lubiprostone (SPI-0211; RU0211) increases intestinal fluid secretion through generation of CIC-2 / CFTR and activation of cAMP signaling pathway. Lubiprostone inhibits myeloperoxidase (MPO) activity, downregulates Indomethacin (HY-14397)-induced iNOS and TNFα expression. Lubiprostone can be used for chronic constipation research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RU-0211; SPI-0211. CAS No. 136790-76-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0679. | |
| Lubiprostone | Lubiprostone is a bicyclic fatty acid metabolite analog of Prostaglandin E1. It activates specific chloride channels in the gastrointestinal tract to stimulate intestinal fluid secretion, increase gastrointestinal transit, and improve symptoms of constipation. Group: Biochemicals. Alternative Names: (11α)-16,16-Difluoro-11-hydroxy-9,15-dioxo-prostan-1-oic Acid; Ru 0211. Grades: Highly Purified. CAS No. 136790-76-6. Pack Sizes: 1mg, 2mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Lubiprostone-[d7] | Lubiprostone-[d7] is the labelled analogue of Lubiprostone, which is a bicyclic fatty acid metabolite analog of Prostaglandin E1. It activates specific chloride channels in the gastrointestinal tract to stimulate intestinal fluid secretion, increase gastrointestinal transit, and improve symptoms of bloating and abdominal discomfort. Synonyms: Lubiprostone D7; (11α)-16,16-Difluoro-11-hydroxy-9,15-dioxo-prostan-1-oic Acid-d7. Grade: 95% by HPLC; 95% atom D. CAS No. 1217675-13-2. Molecular formula: C20H25D7F2O5. Mole weight: 397.51. | |
| Lubricants |  | |
| Lucanthone | Lucanthone is an endonuclease inhibitor of Apurinic endonuclease-1 ( APE-1 ). Uses: Scientific research. Group: Signaling pathways. CAS No. 479-50-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B2098. | |
| Lucanthone Hydrochloride | Anthelmintic (Schistosoma). Group: Biochemicals. Alternative Names: 1-[[2- (Diethylamino) ethyl]amino]-4-methyl-9H-thioxanthen-9-one Hydrochloride; BW 57-233; Lucanthone MonoHydrochloride; Miracil D; Miracol; Ms. 752; NSC 14574; Nilodin; RP 3735; Scapuren; Tixantone. Grades: Highly Purified. CAS No. 548-57-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Lucatumumab | Lucatumumab (HCD122) is a fully human anti-CD40 antagonist monoclonal antibody, which blocks CD40/CD40L-mediated signaling. Lucatumumab efficiently mediates antibody-dependent cell-mediated cytotoxicity (ADCC) and clearance of tumor cells, can be used for refractory lymphomas, CLL and multiple myeloma research [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: HCD122. CAS No. 903512-50-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99167. | |
| Lucerastat | Lucerastat, the galactose form of Miglustat, is an orally-available inhibitor of glucosylceramide synthase (GCS). Lucerastat has the potential for Fabry disease study [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NB-DGJ; N-(n-Butyl)deoxygalactonojirimycin. CAS No. 141206-42-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106392. | |
| Lucidenic acid B | Lucidenic acid B. Group: Biochemicals. Grades: Plant Grade. CAS No. 95311-95-8. Pack Sizes: 5mg. Molecular Formula: C27H38O7, Molecular Weight: 474.59. US Biological Life Sciences. | Worldwide |
| Lucidenic acid C | Lucidenic acid C. Group: Biochemicals. Grades: Plant Grade. CAS No. 95311-96-9. Pack Sizes: 5mg. Molecular Formula: C27H40O7, Molecular Weight: 476.61. US Biological Life Sciences. | Worldwide |
| Lucidenic acid D | Lucidenic acid D, a triterpenoid compound, is extracted from Ganoderma lucidum and is reported to be endowed with multifarious biological activities, such as anti-cancer, anti-inflammatory, and antioxidant properties. With its remarkable potential to stimulate apoptosis in cancer cells, lucidenic acid D stands out as an effective therapeutic candidate for combating cancer and other ailments. Synonyms: Lucidenic acid D; Lucidenic acid D; 298665-16-8; LucidenicacidD; UNII-4C2000605T. Grade: >98%. CAS No. 98665-16-8. Molecular formula: C29H38O8. Mole weight: 514.61. | |
| Lucidenic acid E | Lucidenic acid E. Group: Biochemicals. Grades: Plant Grade. CAS No. 98665-17-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Lucidin | Botanical Source: Group: Biochemicals. Alternative Names: 1,3-Dihydroxy-2-hydroxymethyl-9,10-anthracenedione, 9CI. Grades: Plant Grade. CAS No. 478-08-0. Pack Sizes: 10mg. Molecular Formula: C15H10O5, Molecular Weight: 270.24. US Biological Life Sciences. | Worldwide |
| Lucidone | Lucidone, an anti-inflammatory agent that can be isolated from the fruit of Lindera erythrocarpa Makino. Lucidone inhibits LPS-induced NO and PGE2 production in RAW 264.7 mouse macrophages. Lucidone also decreases TNF-α secretion, iNOS and COX-2 expression. Lucidone prevents NF-κB translocation and inhibits JNK and p38MAPK signals. Lucidone also has inhibitory activity against Dengue virus (DENV) (EC50=25 μM). Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Yellow powder. CAS No. 19956-53-7. Molecular formula: C15H12O4. Mole weight: 256.3. Purity: 0.98. IUPACName: 3-hydroxy-4-methoxy-2-[(E)-3-phenylprop-2-enoyl]cyclopenta-2,4-dien-1-one. Canonical SMILES: COC1=CC(=O)C(=C1O)C(=O)C=CC2=CC=CC=C2. Product ID: ACM19956537. Alfa Chemistry ISO 9001:2015 Certified. Categories: Lucidogen. | |
| Lucifensin | Lucifensin is the key antimicrobial peptide of the green bottle fly larvae Lucilia sericata. This defensin protects the larvae when they are exposed to the infectious environment of a wound during maggot therapy and it also contributes as a disinfectant and healing factor. | |
| Luciferase | Luciferase is an analytical enzyme used as a component of lysis solution to measure luminescence signals. It has been used to investigate the sensitivity of dark mutants of various luminescent bacterial strains to reactive oxygen species. Synonyms: EC 1.14.14.3; Bacterial Luciferase; Luciferase from Photobacterium fischeri. Grade: >95%. CAS No. 9014-00-0. Molecular formula: H14. Mole weight: 14.11. | |
| Luciferase | Luciferase from Vibrio fischeri has also been used in a study to investigate the sensitivity of dark mutants of various strains of luminescent bacteria to reactive oxygen species. Uses: Scientific research. Group: Fluorescent dye. CAS No. 9014-00-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1004. | |
| Luciferase, firefly | Luciferase, firefly is a bioluminescent enzyme responsible for bioluminescence in fireflies and click beetles. Synonyms: Luciferase from Photinus pyralis (firefly). Grade: >98%. CAS No. 61970-00-1. Molecular formula: C18H19N5O. Mole weight: 321.4. | |
| Luciferase, firefly | Luciferase, firefly is the light-emitting enzyme responsible for the bioluminescence of fireflies and click beetles. Uses: Scientific research. Group: Peptides. CAS No. 61970-00-1. Pack Sizes: 1 mg. Product ID: HY-P1004A. | |
| Luciferase from E. coli, Recombinant | Luciferase is an enzyme that catalyzes production of light from luciferin in the presence of Mg2+-ATP and oxygen. The reaction of this enzyme with luciferin, ATP, and O2 results in the emission of light. Luciferase activity can be inhibited by general anesthetics including isoflurane and ketamine/medetomidine thereby affecting the sensitivity of bioluminescence imaging. Group: Enzymes. Synonyms: Photinus-luciferin 4-monooxygenase (ATP-hydrolysing); firefly luciferase; luciferase (firefly luciferin); Photinus luciferin 4-monooxygenase (adenosine triphosphate-hydrolyzing); firefly luciferin luciferase; Photinus pyralis luciferase; EC 1.13.12.7; 61970-00-1. Enzyme Commission Number: EC 1.13.12.7. Luciferase. Mole weight: ca. 60 kDa. Activity: > 1.0 x 10^9 relative light units (RLU)/mg lyophilizate Specific activity: 1.4 x 10^11 RLU/mg purified protein. Stability: stable at 25°C for at least 5 days (liquid form). Appearance: White lyophilizate. Storage: at -20°C. Source: E. coli. Species: E. coli. Photinus-luciferin 4-monooxygenase (ATP-hydrolysing); firefly luciferase; luciferase (firefly luciferin); Photinus luciferin 4-monooxygenase (adenosine triphosphate-hydrolyzing); firefly luciferin luciferase; Photinus pyralis luciferase; EC 1.13.12.7; 61970-00-1. Cat No: NATE-1253. |  |
| Luciferase from Photinus pyralis (firefly), Recombinant | Firefly luciferase is an enzyme that catalyzes production of light from luciferin in the presence of Mg2+-ATP and oxygen. The reaction of this enzyme with luciferin, ATP, and O2 results in the emission of light. Luciferase activity can be inhibited by general anesthetics including isoflurane and ketamine/medetomidine thereby affecting the sensitivity of bioluminescence imaging. Applications: The reaction of this enzyme with luciferin, atp, and o2 results in the emission of light. luciferase can be used to detect trace amounts of atp. firefly luciferase is also one of the most commonly utilized reporter genes for the study of gene expression. the bioluminescent rea...pe I , > 5 ,000 ,000 units/mg protein; Type II, 15-30×106 light units/mg protein. Storage: -70°C. Form: Type I, Supplied as a solution in 50 mM Tris HCl pH 8.0, 1 mM dithiothreitol, 1 mM EDTA, and 10% (v/v) glycerol; Type II, Lyophilized powder approximately 20% protein; balance is primarily NaCl, HEPES buffer salts, and carbohydrate. Source: E. coli. Species: Photinus pyralis (firefly). Photinus-luciferin 4-monooxygenase (ATP-hydrolysing); firefly luciferase; luciferase (firefly luciferin); Photinus luciferin 4-monooxygenase (adenosine triphosphate-hydrolyzing); firefly luciferin luciferase; Photinus pyralis luciferase; EC 1.13.12.7; 61970-00-1. Cat No: NATE-0424. | |
| Luciferase from Vibrio fischeri | Luciferase from Vibrio fischeri. Group: Biochemicals. Grades: Highly Purified. CAS No. 9014-00-0. Pack Sizes: 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| Luciferase from Vibrio fischeri (Photobacterium f) | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Luciferase-IN-4 | Luciferase-IN-4 (Compound 6b) is an inhibitor for luciferase with IC 50 of 4.1 μM. Luciferase-IN-4 inhibits purified luciferase in P. pyralis with IC 50 of 2.0 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1020413-85-7. Pack Sizes: 1 mg. Product ID: HY-161475. | |
| Lucifer Yellow CH dilithium salt | fluorescent stain. Group: Fluorescence/luminescence spectroscopy. | |
| Lucifer Yellow CH dipotassium salt | Lucifer Yellow CH dipotassium is a high-intensity fluorescent probe containing free hydrazyl groups. Lucifer Yellow CH can react with fatty aldehydes at room temperature. Lucifer Yellow CH serves as a biological tracer to monitor neuronal branching, regeneration, gap junction detection and characterization, and selective ablation of cells after aldehyde fixation. Lucifer yellow CH displays the maximum excitation/emission of 430 nm/540 nm, respectively [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 71206-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-W127715. | |
| Lucifer Yellow CH dipotassium salt | powder. Group: Fluorescence/luminescence spectroscopy. | |
| Lucifer yellow vs dilithium salt | Lucifer yellow vs dilithium salt. Group: Bioelectronic materials other materials. Alternative Names: 4-AMINO-N-[3- (VINYLSULFONYL)-PHENYL]NAPHTHALIMIDE-3, 6-DISULFONATE DILITHIUM SALT; LUCIFER YELLOW VS; LUCIFER YELLOW VS DILITHIUM SALT; DILITHIUM 4-AMINO-N-[3- (VINYLSULFONYL)PHENYL]NAPHTHALIMIDE-3, 6-DISULFONATE; LUCIFER YELLOW VS DILITHIUM SALT, FOR FL UORESCE. CAS No. 71231-14-6. Product ID: dilithium; 6-amino-2-(3-ethenylsulfonylphenyl)-1,3-dioxobenzo[de]isoquinoline-5,8-disulfonate. Molecular formula: 550.5g/mol. Mole weight: C20H12Li2N2O10S3. [Li+]. [Li+]. C=CS (=O) (=O)C1=CC=CC (=C1)N2C (=O)C3=CC (=CC4=C3C (=CC (=C4N)S (=O) (=O)[O-])C2=O)S (=O) (=O)[O-]. InChI=1S/C20H14N2O10S3. 2Li/c1-2-33 (25, 26)11-5-3-4-10 (6-11)22-19 (23)14-8-12 (34 (27, 28)29)7-13-17 (14)15 (20 (22)24)9-16 (18 (13)21)35 (30, 31)32; ; /h2-9H, 1, 21H2, (H, 27, 28, 29) (H, 30, 31, 32); ; /q; 2*+1/p-2. PSJNJVOFDDMXDP-UHFFFAOYSA-L. |  |
| Lucigenin | Lucigenin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N'-Dimethyl-9,9'-biacridiniumdinitrate. Product Category: Other Fluorophores. Appearance: Off-white to brown powder. CAS No. 2315-97-1. Molecular formula: C28H22N4O6. Mole weight: 510.5. Purity: 98%+. IUPACName: 10-methyl-9-(10-methylacridin-10-ium-9-yl)acridin-10-ium;dinitrate. Canonical SMILES: C[N+]1=C2C=CC=CC2=C(C3=CC=CC=C31)C4=C5C=CC=CC5=[N+](C6=CC=CC=C64)C.[N+](=O)([O-])[O-].[N+](=O)([O-])[O-]. Product ID: ACM2315971-1. Alfa Chemistry ISO 9001:2015 Certified. | |
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