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| Product | Description | |
|---|---|---|
| Lodenafil carbonate | Lodenafil carbonate, a dimer that acts as a proagent delivering Lodenafil in vivo, is an orally active phosphodiesterase type 5 (PDE5) inhibitor for the treatment of erectile dysfunction (ED) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 398507-55-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-108045. |  |
| Lodenafil Carbonate | Lodenafil carbonate is a new PDE-5 inhibitor used for oral therapy in erectile dysfunction. Group: Biochemicals. Alternative Names: 5, 5'-[Carbonylbis[oxy-2, 1-ethanediyl-4, 1-piperazinediylsulfonyl (6-ethoxy-3, 1-phenylene)]]bis[1, 6-dihydro-1-methyl-3-propyl-7H-pyrazolo[4, 3-d]pyrimidin-7-one; 4-[[3-(4,7-Dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-4-ethoxyphenyl]sulfonyl]-1-piperazineethanol Carbonate Ester. Grades: Highly Purified. CAS No. 398507-55-6. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Lodenafil Carbonate | Cas No. 398507-55-6. |  |
| Lodoxamide | Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-42585E free acid. CAS No. 53882-12-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-14270. | |
| Lodoxamide | Lodoxamide is a potent agonist of GPR35 and an antiallergic drug. It can be used as a mast cell stabilizer for topical administration into eyes indicated for allergic synptom treatment. Uses: Anti-allergic agents. Synonyms: 2-[2-chloro-5-cyano-3-(oxaloamino)anilino]-2-oxoacetic acid. Grades: ≥95%. CAS No. 53882-12-5. Molecular formula: C11H6ClN3O6. Mole weight: 311.6. | |
| Lodoxamide | N,N-(2-chloro-5-cyano-m-phenylene) dioxamic acid tromethamine salt Alomide. CAS No. 53882-12-5. Product ID: 8-01420. Molecular formula: C19H28O12N5Cl. Mole weight: 553.91. |  |
| Lodoxamide | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Lodoxamide | Lodoxamide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,2-[(2-Chloro-5-cyano-1,3-phenylene)diimino]bis[2-oxoacetic acid];Acetic acid, 2,2-((2-chloro-5-cyano-1,3-phenylene)diimino)bis(2-oxo-;Lodoxamida;Lodoxamida [inn-spanish];Lodoxamidum;Lodoxamidum [inn-latin];N,N-(2-Chlor-5-cyan-3-phenylen)dioxamsaeure;Unii-spu695od73. Product Category: Heterocyclic Organic Compound. CAS No. 53882-12-5. Molecular formula: C11H6ClN3O6. Mole weight: 0. Product ID: ACM53882125. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Lodoxamide tromethamine | Lodoxamide is a GPR35 agonist that has been used as a mast cell stabilizer. It can be used for topical administration into eyes indicated for allergic symptom treatment. Synonyms: Alomide; Lodoxamidetromethamine. CAS No. 63610-09-3. Molecular formula: C19H28ClN5O12. Mole weight: 553.9. | |
| Lodoxamide tromethamine | Lodoxamide tromethamine (U-42585E) is a medication for the treatment of prophylaxis of mast cell-mediated allergic disease. Uses: Scientific research. Group: Signaling pathways. Alternative Names: U-42585E. CAS No. 63610-09-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16289. | |
| Lodoxamide Tromethamine | antifungal polyene macrolide that is active in the cell membrane soluble 5% Acetic acid. CAS No. 63610-09-3. Product ID: 8-01366. Molecular formula: C11H6ClN3O6 2C4H11NO3. Mole weight: 553.91. Reference: Merck Index, 12: 6513; Appl. Environ. Microbiol., 58, 1064, 1992. | |
| LOE 908 hydrochloride | LOE 908 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 143482-60-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| LOE 908 hydrochloride | LOE 908 hydrochloride is a broad spectrum cation channel blocker. It can inhibit several cation channels including store-operated calcium channels, voltage-operated calcium channels and so on. LOE 908 hydrochloride can reduce cortical infarct size and improve neurological outcome following middle cerebral artery occlusion. Synonyms: LOE908 hydrochloride; LOE-908 hydrochloride; 3,4-Dihydro-6,7-dimethoxy-α-phenyl-N,N-bis[2-(2,3,4-trimethoxyphenyl)ethyl]-1-isoquinolineacetamide hydrochloride; 1-Isoquinolineacetamide, 3,4-dihydro-6,7-dimethoxy-α-phenyl-N,N-bis[2-(2,3,4-trimethoxyphenyl)ethyl]-, hydrochloride (1:1); 1-Isoquinolineacetamide, 3,4-dihydro-6,7-dimethoxy-α-phenyl-N,N-bis[2-(2,3,4-trimethoxyphenyl)ethyl]-, monohydrochloride; LOE 908 monohydrochloride. Grades: ≥95%. CAS No. 143482-60-4. Molecular formula: C41H48N2O9.HCl. Mole weight: 749.29. | |
| Lofepramine | Lofepramine is a serotonin and noradrenalin reuptake inhibitor as an antidepressant. Synonyms: 1-(4-Chlorophenyl)-2-[[3-(10,11-dihydro-5H-dibenz(Z)[b,f]azepin-5-yl)propyl]methylamino]ethanone. Grades: ≥99% by HPLC. CAS No. 23047-25-8. Molecular formula: C26H27N2OCl. Mole weight: 418.97. | |
| Lofepramine | Psychotropic drug related to imipramine. Antidepressant. Group: Biochemicals. Alternative Names: 1- (4-Chlorophenyl) -2- [ [3- (10, 11-dihydro-5H-dibenz [b, f] azepin-5-yl) propyl] methylamino] ethanone; 4'-Chloro-2- [ [3- (10, 11-dihydro-5H-dibenz [b, f] azepin-5-yl) propyl-methylamino] acetophenone. Grades: Highly Purified. CAS No. 23047-25-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Lofepramine | Lofepramine (Lopramine) is a modified tricyclic and orally active antidepressant. Lofepramine inhibits the uptake of Noradrenaline (NA) (HY-13715) and 5-hydroxytryptamine (5-HT) with IC 50 s of 2.7 μM and 11 μM, respectively. Lofepramine exerts its antidepressant activity by promoting noradrenergic neurotransmission. Lofepramine also enhances serotonergic neurotransmission by inhibiting neuronal uptake of 5-HT and tryptophan pyrrolase. Lofepramine exhibits significant anxiolytic properties. [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lopramine. CAS No. 23047-25-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12390. | |
| lofepramine hydrochloride | Lofepramine is a tricyclic antidepressant (TCA) indicated for the treatment of depression. It functions via inhibiting 5-HT and NA reuptake. Synonyms: N-(4-CHLOROBENZOYLMETHYL)-3-(10,11-DIHYDRO-5H-DIBENZ[B,F]AZEPIN-5-YL)-N-METHYLPROPYLAMINE HYDROCHLORIDE; LOFEPRAMINE HCL; LOFEPRAMINE HYDROCHLORIDE; 4'-chloro-2-((3-(10,11-dihydro-5h-dibenz(b,f)azepin-5-yl)propyl)methylamino); acetophenone,4'-chloro-2-((3-(1. Grades: 95%. CAS No. 26786-32-3. Molecular formula: C26H28Cl2N2O. Mole weight: 455.426. | |
| Lofexidine | Lofexidine is a selective α2-receptor agonist, commonly used to alleviate the physical symptoms of heroin and other types of opioid withdrawal [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 31036-80-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B1052A. | |
| Lofexidine | Lofexidine. CAS No. 31036-80-3. Product ID: 8-01727. Molecular formula: C11H12Cl2N2O. Mole weight: 272.13. Purity: 0.99. | |
| Lofexidine-d4 hydrochloride | Lofexidine-d4 hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-[1-(2,6-Dichlorophenoxy)ethyl]-4,5-dihydro-. Product Category: Heterocyclic Organic Compound. Appearance: Off-White Solid. CAS No. 78302-26-8. Molecular formula: C11H9D4Cl3N2O. Mole weight: 299.62. Product ID: ACM78302268. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lofexidine-d4 Hydrochloride | α2-Adrenoceptor agonist related structurally to Clonidine. Used in treatment of opioid withdrawal symptoms; antihypertensive. Group: Biochemicals. Alternative Names: 2-[1-(2,6-Dichlorophenoxy)ethyl]-4,5-dihydro-. Grades: Highly Purified. CAS No. 78302-26-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Lofexidine hydrochloride | Lofexidine hydrochloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LOFETENSIN,LOXACOR;LOFEXIDINE HCL;LOFEXIDINE, HYDROCHLORIDE;MDL-14042A;BA-168;BRITLOFEX;2-[1-(2,6-dichlorophenoxy)ethyl]-2-imidazoline hydrochloride;2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1h-imidazole hydrochloride. Product Category: Heterocyclic Organic Compound. Appearance: Crystalline Solid. CAS No. 21498-08-8. Molecular formula: C11H12Cl2N2O?HCl. Mole weight: 295.59. Purity: ≥98%. Density: g/cm³. Product ID: ACM21498088. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lofexidine hydrochloride | Lofexidine (hydrochloride) is a selective α2-receptor agonist, commonly used to alleviate the physical symptoms of heroin and other types of opioid withdrawal [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Baq-168; MDL-14042. CAS No. 21498-08-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1052. | |
| Lofexidine hydrochloride | Lofexidine hydrochloride. Group: Biochemicals. Alternative Names: 2-[1-(2,6-Dichlorophenoxy)ethyl]-4,5-dihydro-1H-imidazole Hydrochloride. Grades: Highly Purified. CAS No. 21498-08-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C11H13Cl3N2O. US Biological Life Sciences. | Worldwide |
| Lofexidine hydrochloride | Lofexidine hydrochloride is the hydrochloride salt form of Lofexidine. Lofexidine, an analogue of clonidine, is an α2A-adrenergic receptor agonist for the treatment of opioid withdrawal symptoms as well as an anihypertensive. Uses: α2-adrenoceptor agonist related structurally to clonidine. used in treatment of opioid withdrawal symptoms; antihypertensive. Synonyms: 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1H-imidazole;hydrochloride 2-(alpha-(2,6-dichlorophenoxy)ethyl) delta-2-imidazoline BritLofex lofexidine lofexidine hydrochloride Lofexidine mono-hydrochloride lofexidine monohydrochloride lofexidine, (+-)-isom. Grades: ≥98%. CAS No. 21498-08-8. Molecular formula: C11H13Cl3N2O. Mole weight: 295.59. | |
| Lofexidine Hydrochloride | Lofexidine Hydrochloride. CAS No. 21498-08-8. Product ID: 8-01728. Molecular formula: C11H12Cl2N2O HCl. Mole weight: 295.6. | |
| Lofexidine Hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyapi standardspharmaceutical toxicology. Alternative Names: Loxacor, Lofexidine hydrochloride, 1H-Imidazole, 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-, monohydrochloride (9CI), 2-Imidazoline, 2-[1-(2,6-dichlorophenoxy)ethyl]-, monohydrochloride (8CI), MDL 14042,1H-Imidazole, 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-, hydrochloride (1:1), Baq 168, Lofetensin, Britlofex. | |
| Lofexidine, Hydrochloride (MDL-14042A, Ba-168, Britlofex, Lofetensin,Loxacor) | A vasoactive agent related structurally to Clonidine. Group: Biochemicals. Alternative Names: MDL-14042A, Ba-168, Britlofex, Lofetensin,Loxacor. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Loflucarban | Loflucarban is an antifungal agent. Synonyms: Loflucarban; NSC 76851; NSC-76851; NSC76851; Fluonilid; Fluonilide; 3,5-Dichloro-4'-fluorothiocarbanilide; 1-(3,5-dichlorophenyl)-3-(4-fluorophenyl)thiourea. CAS No. 790-69-2. Molecular formula: C13H9Cl2FN2S. Mole weight: 315.187. | |
| loganate O-methyltransferase | Also acts on secologanate. Methylates the 11-carboxy group of the monoterpenoid loganate. Group: Enzymes. Synonyms: loganate methyltransferase; S-adenosyl-L-methionine:loganic acid methyltransferase. Enzyme Commission Number: EC 2.1.1.50. CAS No. 39391-10-1. 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-1954; loganate O-methyltransferase; EC 2.1.1.50; 39391-10-1; loganate methyltransferase; S-adenosyl-L-methionine:loganic acid methyltransferase. Cat No: EXWM-1954. |  |
| Loganic acid | Loganic acid. Group: Biochemicals. Alternative Names: Norloganin. Grades: Plant Grade. CAS No. 22255-40-9. Pack Sizes: 20mg. Molecular Formula: C16H24O10, Molecular Weight: 376.355999999999. US Biological Life Sciences. | Worldwide |
| Loganin | Loganin. Group: Biochemicals. Alternative Names: Meliatin; Loganoside. Grades: Plant Grade. CAS No. 18524-94-2. Pack Sizes: 20mg. Molecular Formula: C17H26O10, Molecular Weight: 390.382. US Biological Life Sciences. | Worldwide |
| Loganin | analytical standard. Group: Chemical classcarbohydrates. | |
| Loganin | Loganin is a type of iridoid glycoside compound that possesses anti-inflammatory, antioxidant, and antitumor properties, and offers protective effects against acute lung injury and pulmonary fibrosis. Loganin exerts its protective effects against LPS (HY-D1056)-mediated inflammation and oxidative stress by upregulating the Nrf2/HO-1 signaling pathway, and it reduces neuroinflammation caused by spinal cord injury (SCI) [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. Alternative Names: Loganoside. CAS No. 18524-94-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0512. | |
| Logwood Extract | Logwood Extract. Applications: Used as coloring in the production of beverage, food, supplement and cosmetic industry. Group: Others. Synonyms: Logwood Extract; Haematoxylum campechianum L. Purity: 5-10:1 By TLC. Appearance: Black fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Wood. Species: Haematoxylum campechianum L. Logwood Extract; Haematoxylum campechianum L.; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-119. | |
| LOK (1-348), active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Lok1 active human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Lokivetmab | Lokivetmab (Anti-Canine IL31 Recombinant Antibody) is an anti-canine IL-31 monoclonal antibody that can be used for the research of atopic dermatitis (AD) in dogs [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Canine IL31 Recombinant Antibody. CAS No. 1533403-95-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99301. | |
| Lolamicin | Lolamicin is a Gram-negative specific antibiotic. Lolamicin is active against more than 130 multidrug-resistant clinical isolates, has shown efficacy in multiple mouse models of acute pneumonia and sepsis infection, and protects the gut microbiome of mice against secondary infection with Clostridium difficile. The selective killing of pathogenic gram-negative bacteria by Lolamicin is a result of the low sequence homology of pathogenic bacteria and symbiotic bacteria. Lolamicin can be used in the study of infection caused by Gram-negative pathogens [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2930690-12-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-164036. | |
| L-olivosyl-oleandolide 3-O-methyltransferase | The enzyme is involved in the biosynthesis of the macrolide antibiotic oleandomycin in Streptomyces antibioticus. It can also act on other monoglycosylated macrolactones, including L-rhamnosyl-erythronolide B and L-mycarosyl-erythronolide B. Group: Enzymes. Synonyms: OleY. Enzyme Commission Number: EC 2.1.1.239. 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-1842; L-olivosyl-oleandolide 3-O-methyltransferase; EC 2.1.1.239; OleY. Cat No: EXWM-1842. | |
| Lomatium Dissectum Root (Whole) & (Cut & Sifted) | Lomatium Dissectum Root (Whole) & (Cut & Sifted). |  CA, FL & NJ |
| Lombartinib impurity2 | Lombartinib impurity2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1069122-99-1. Molecular formula: C7H7ClN2O2. Mole weight: 186.6. Catalog: APB1069122991. | |
| Lombazole | Lombazole is used as an antimicrobial agent of the imidazole class. Uses: Lombazole is used as an antimicrobial agent of the imidazole class. Synonyms: Bay h 6020; Lombazolum; Lombazol; 1-([1,1'-biphenyl]-4-yl(2-chlorophenyl)methyl)-1H-imidazole; (2-Chlorophenyl)-imidazol-1-yl-(biphenyl-4-yl)methane. Grades: 98%. CAS No. 60628-98-0. Molecular formula: C22H17ClN2. Mole weight: 344.84. | |
| lombricine kinase | Also acts on methylated lombricines such as thalassemine; the specificity varies with the source species. Group: Enzymes. Enzyme Commission Number: EC 2.7.3.5. CAS No. 9026-53-3. 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-3185; lombricine kinase; EC 2.7.3.5; 9026-53-3. Cat No: EXWM-3185. | |
| Lomefloxacin | Lomefloxacin is a bactericidal fluoroquinolone agent with activity against a wide range of gram-negative and gram-positive organisms, which is commonly used to treat bacterial infections, including bronchitis and urinary tract infections. It is used as a pre-operative prophylactic to prevent urinary tract infection caused by S. pneumoniae, H. influenzae, S. aureus, P. aeruginosa, E. cloacae, P. mirabilis, C. civersus, S. asprphyticus, E. coli, and K. pneumoniae. It is used to induce genomic instability in mice1 and modification of the kinetics of growth of Gram-negative bacteria. It inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, which are needed for the transcription and replication of bacterial DNA. Uses: Anti-bacterial agents. Synonyms: Maxaquin; SC47111A. Grades: >98%. CAS No. 98079-51-7. Molecular formula: C17H19F2N3O3. Mole weight: 351.35. | |
| Lomefloxacin·HCl 99+% (HPLC) | Lomefloxacin·HCl 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Lomefloxacin hydrochloride | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C17H19F2N3O3 · HCl. CAS No. 98079-51-7. Prepack ID 39370200-1g. Molecular Weight 387.81. See USA prepack pricing. |  |
| Lomefloxacin hydrochloride | Lomefloxacin (SC47111A) hydrochloride is a broad-spectrum quinolone antibiotic , with antimicrobial activity. Lomefloxacin hydrochloride is used for the research of respiratory tract infections, genitourinary infections, gastrointestinal infections, ENT infections, etc. [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SC47111A hydrochloride. CAS No. 98079-52-8. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0455. | |
| Lomefloxacin, Hydrochloride | Fluorinated quinolone antibacterial. DNA gyrase antagonist. Lomefloxacin HCl is a hydrochloride salt of lomefloxacin and is a fluoroquinolone antibiotic. Lomefloxacin is an orally bioavailable, broad-spectrum fluoroquinolone antibiotic.1 In vitro, it inhibits growth of N. gonorrhoeae, E. coli, K. pneumoniae, P. vulgaris, S. epidermidis, and M. morganii (MIC90s = 0.1, 0.39, 0.39, 0.39, 0.39, and 0.78ug/ml, respectively). It also inhibits growth of S. aureus and methicillin-resistant S. aureus (MRSA; MIC90 = 3.13ug/ml for both) and of H. influenzae and ampicillin-resistant H. influenzae (MIC90 = 0.1ug/ml for both). In vivo, lomefloxacin inhibits the growth of P. mirabilis, E. coli, K. pneumoniae, and S. aureus (ED50s = 1.39, 1.45, 1.78, and 6.66mg/kg, respectively) in mouse models of systemic infection. It inhibits bacterial DNA gyrase, thereby inhibiting DNA synthesis and bacterial growth.2 Formulations containing lomefloxacin have been used in the treatment of bronchitis and urinary tr Group: Biochemicals. Alternative Names: 1-Ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic Acid Hydrochloride; Alkaflox; Bareon; Chimono; Lomebact; Lomef 400; Lomflox; Lomitas; Lomoxin; Maxaquin; Mazaquin; NY 198; Orchacin; SC 47111; Uniquin. Grades: Highly Purified. CAS No. 98079-52-8. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C17H20ClF2N3O3, Molecular Weight: 387.81. US Biological Life Sciences. | Worldwide |
| Lomeguaritrib | Lomeguaritrib. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 6-(4-Bromothenyloxy)-7H-purin-2-amine. Product Category: Thiophenes. Appearance: Off-White Solid. CAS No. 192441-08-0. Molecular formula: C10H8BrN5OS. Mole weight: 326.17. Purity: 95%+. Product ID: ACM192441080. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lomeguatrib | Lomeguatrib is an inhibitor of O6-methylguanine-DNA methyltransferase (MGMT). Lomeguatrib attenuates MGMT activity in vitro and in vivo. Lomeguatrib enhances the antitumor activity of temozolomide in both human melanoma and MCF-7 xenografts. Group: Biochemicals. Alternative Names: 6-[(4-Bromo-2-thienyl)methoxy]-9H-purin-2-amine; 6-[(4-Bromo-2-thienyl)methoxy]-1H-purin-2-amine; 2-Amino-6-(4-bromothiophen-2-ylmethoxy)-9H-purine; PaTrin 2. Grades: Highly Purified. CAS No. 192441-08-0. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Lomeguatrib | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lomeguatrib | Lomeguatrib, also known as PaTrin-2, is a potent Inhibitor of O6-Alkylguanine-DNA-Alkyltransferase. Lomeguatrib is also a nontoxic low-molecular weight pseudosubstrate that has the ability to inactivate MGMT. Lomeguatrib can be used with temozolomide (TMZ) for GBM treatment. Synonyms: PaTrin 2; PaTrin2; PaTrin-2; Lomeguatrib; Patrin. O6-(4-bromothenyl)guanine; 6-(4-Bromothenyloxy)-7H-purin-2-amine. CAS No. 192441-08-0. Molecular formula: C10H8BrN5OS. Mole weight: 326.172. | |
| Lomeguatrib | Lomeguatrib is a O6-methylguanine-DNA methyltransferase (MGMT) inhibitor, with IC50s of 9 nM in cell-free assay and ?6?nM in MCF-7 cells. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PaTrin-2. CAS No. 192441-08-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13668. | |
| Lomerizine dihydrochloride | Lomerizine dihydrochloride is an antagonist of L- and T-type voltagegated calcium channels. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KB-2796. CAS No. 101477-54-7. Pack Sizes: 10 mM * 1 mL; 10 mg; 50 mg; 100 mg. Product ID: HY-B0768A. | |
| Lomerizine dihydrochloride | This product is a diphenylpiperazine calcium channel blocker with selective cerebral vasodilation. Synonyms: 1- (4, 4'-Difluorobenzhydryl) -4- (2, 3, 4-trimethoxybenzyl) piperazine·dihydrochloride; Flometizinehydrochloride; Lomerizinedihydrochloride, 99%, anewL-andT-typecalciumchannelblocker; Lomerizine2HCl; KB-2796dihydrochlorideChemicalbook; Piperazine, 1-[bis (4-fluorophenyl) methyl]-4-[ (2, 3, 4-trimethoxyphenyl) methyl]-, hydrochloride (1: 2) ; Lomerizinedihydrochloride, >=99%; 1- (Bis (4-fluorophenyl) methyl) -4- (2, 3, 4-trimethoxybenzyl) piperazinedihydrochloride. CAS No. 101477-54-7. Product ID: PAP-0072. Molecular formula: C27H32Cl2F2N2O3. Category: Cardiovascular. Product Keywords: Cardiovascular Series; Lomerizine dihydrochloride; PAP-0072; Cardiovascular; C27H32Cl2F2N2O3; 101477-54-7. Appearance: white to tan. Standard: CP. Chemical Name: 1- (4, 4'-Difluorobenzhydryl) -4- (2, 3, 4-trimethoxybenzyl) piperazine·dihydrochloride. Grade: Pharmaceutical Grade. Solubility: DMSO: ≥30mg/mL. Storage: Inert atmosphere,2-8°C. Product Description: This product is a diphenylpiperazine calcium channel blocker with selective cerebral vasodilation. |  |
| Lomerizine Dihydrochloride | Lomerizine dihydrochloride, an L- and T-type voltagegated calcium channel blocker, is a selective cerebral vasodilator and antimigraine. Uses: Calcium channel blockers. Synonyms: KB-2796; 1-(2,3,4-Trimethoxybenzyl)-4-(bis(4-fluorophenyl)methyl)piperazine dihydrochloride; Terranas; Piperazine, 1-[bis(4-fluorophenyl)methyl]-4-[(2,3,4-trimethoxyphenyl)methyl]-, hydrochloride (1:2); KB 2796; KB2796. Grades: >98%. CAS No. 101477-54-7. Molecular formula: C27H30F2N2O3.2HCl. Mole weight: 541.46. | |
| Lomerizine Dihydrochloride | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopyneurochemicals. | |
| Lomerizine Dihydrochloride, 98% | Lomerizine Dihydrochloride, 98%. Group: other glass and ceramic materials. CAS No. 101477-54-7. Product ID: 1-[bis(4-fluorophenyl)methyl]-4-[(2,3,4-trimethoxyphenyl)methyl]piperazine; dihydrochloride. Molecular formula: 541.5g/mol. Mole weight: C27H32Cl2F2N2O3. COC1=C (C (=C (C=C1)CN2CCN (CC2)C (C3=CC=C (C=C3)F)C4=CC=C (C=C4)F)OC)OC. Cl. Cl. InChI=1S/C27H30F2N2O3. 2ClH/c1-32-24-13-8-21 (26 (33-2)27 (24)34-3)18-30-14-16-31 (17-15-30)25 (19-4-9-22 (28)10-5-19)20-6-11-23 (29)12-7-20; ; /h4-13, 25H, 14-18H2, 1-3H3; 2*1H. LOGVKVSFYBBUAJ-UHFFFAOYSA-N. |  |
| Lomerizine, Dihydrochloride (KB-2796, Terranas) | A diphenylpiperazine calcium channel blocker. A selective cerebral vasodilator. Group: Biochemicals. Alternative Names: KB-2796; Terranas; 1-[bis (4-fluorophenyl) methyl]-4-[ (2, 3, 4-trimethoxyphenyl) methyl]piperazine. Grades: Highly Purified. CAS No. 101477-54-7. Pack Sizes: 10mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Lomerizine Impurity 1 | Grades: > 95%. Molecular formula: C26H28F2N2O3. Mole weight: 454.52. | |
| Lomerizine Impurity 2 | Grades: > 95%. Molecular formula: C26H28F2N2O3. Mole weight: 454.52. | |
| Lomerizine Impurity 3 | Grades: > 95%. Molecular formula: C28H32F2N2O3. Mole weight: 482.58. | |
| Lometraline HCl | Lometraline, an aminotetralin derivative, is a potential antidepressant and/or anxiolytic agent. Uses: A potential antidepressant and/or anxiolytic agent. Synonyms: 8-chloro-5-methoxy-N,N-dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine;hydrochloride. Grades: ≥98%. CAS No. 34552-78-8. Molecular formula: C13H19Cl2NO. Mole weight: 276.20. | |
| Lometrexol | Lometrexol is a folate analog antimetabolite with antineoplastic activity. As the 6R diastereomer of 5,10-dideazatetrahydrofolate, lometrexol inhibits glycinamide ribonucleotide formyltransferase (GARFT), the enzyme that catalyzes the first step in the de novo purine biosynthetic pathway, thereby inhibiting DNA synthesis, arresting cells in the S phase of the cell cycle, and inhibiting tumor cell proliferation. The agent has been shown to be active against tumors that are resistant to the folate antagonist methotrexate. Uses: Antimetabolites, antineoplastic. Synonyms: Lometrexol; LMTX; LY 264618; LY-264618; LY264618. CAS No. 106400-81-1. Molecular formula: C21H25N5O6. Mole weight: 443.46. | |
| Lometrexol | Lometrexol (DDATHF), an antipurine antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and apoptosis, even cell cycle arrest. Lometrexol has anticancer activity. Lometrexol also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DDATHF. CAS No. 106400-81-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14521. | |
| Lometrexol disodium | Lometrexol is a folate analog antimetabolite with antineoplastic activity. Synonyms: LY 264618 disodium; LY264618 disodium; NSC-722969; NSC 722969; L-Glutamic acid, N-(4-(2-((6R)-2-amino-1,4,5,6,7,8-hexahydro-4-oxopyrido(2,3-d)pyrimidin-6-yl)ethyl)benzoyl)-, disodium salt. Grades: 98%. CAS No. 120408-07-3. Molecular formula: C21H23N5Na2O6. Mole weight: 487.42. | |
| Lometrexol hydrate | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lomevactone | Lomevactone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Lomevactone, Lomevactone [INN], UNII-TP71SPS85C, CID100079, LS-127471, (3-alpha,4-beta,6-alpha)-Tetrahydro-4-(4-chlorophenyl)-6-methyl-3-phenyl-2H-pyran-2-one, Chloro-4 phenyl-4 methyl-6 phenyl-3 tetrahydro-3,4,5,6 pyrone-6 (3R*,4S*,6R*) [French], 2H-Pyran-2-one, tetrahydro-4-(4-chlorophenyl)-6-methyl-3-phenyl-, (3-alpha,4-beta,6-alpha)-, Chloro-4 phenyl-4 methyl-6 phenyl-3 tetrahydro-3,4,5,6 pyrone-6 (3R*,4S*,6R*), 75115-73-0, 81478-25-3. Product Category: Heterocyclic Organic Compound. CAS No. 81478-25-3. Molecular formula: C18H17ClO2. Mole weight: 300.783. Purity: 0.96. IUPACName: 4-(4-chlorophenyl)-6-methyl-3-phenyloxan-2-one. Canonical SMILES: CC1CC(C(C(=O)O1)C2=CC=CC=C2)C3=CC=C(C=C3)Cl. Density: 1.182g/cm³. Product ID: ACM81478253. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lomibuvir | Lomibuvir is an nonnucleoside NS5B polymerase inhibitor. It inhibits the 1b/Con1 HCV subgenomic replicon. It binds to the HCV polymerase with dissociation constants of 17 nM. It demonstrated effective antiviral efficacy and may be used for the treatment of HCV. It was developed by ViroChem Pharma, which was acquired by Vertex Pharmaceuticals in 2009. It is in clinical phase 2 with no progress. Uses: Lomibuvir demonstrated effective antiviral efficacy and may be used for the treatment of hcv. Synonyms: 2-Thiophenecarboxylic acid, 5-(3,3-dimethyl-1-butyn-1-yl)-3-[(trans-4-hydroxycyclohexyl)[(trans-4-methylcyclohexyl)carbonyl]amino]-; 5-(3,3-Dimethyl-1-butyn-1-yl)-3-[(trans-4-hydroxycyclohexyl)[(trans-4-methylcyclohexyl)carbonyl]amino]-2-thiophenecarboxylic acid; 5- (3, 3-Dimethyl-1-butynyl) -3-[ (trans-4-hydroxycyclohexyl) [ (trans-4-methylcyclohexyl) carbonyl]amino]thiophene-2-carboxylic acid; VCH 222; VX 222. Grades: >98 %. CAS No. 1026785-55-6. Molecular formula: C25H35NO4S. Mole weight: 445.62. | |
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