A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Eniporide | Eniporide is a potent and selective inhibitor of human Na+/H+ exchanger isoform 1 (NHE-1) (IC50 = 4.5 nM). Synonyms: N-(diaminomethylidene)-2-methyl-5-methylsulfonyl-4-pyrrol-1-ylbenzamide. Grades: ≥95%. CAS No. 176644-21-6. Molecular formula: C14H16N4O3S. Mole weight: 320.4. |  |
| Eniporide hydrochloride | Eniporide hydrochloride (EMD-96785 hydrochloride) is a potent Na + /H + exchange inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EMD-96785 hydrochloride. CAS No. 211813-86-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106150B. |  |
| Enisamium iodide | Enisamium iodide is an anti-influenza compound. Synonyms: N-benzyl-1-methylpyridin-1-ium-4-carboxamide;iodide; Enisamium iodide; brand name: Amizon. Grades: >98%. CAS No. 201349-37-3. Molecular formula: C14H15N2O.I. Mole weight: 354.19. | |
| Enkelytin | The antibacterial spectrum shows that enkelytin is active against several Gram-positive bacteria including Staphylococcus aureus, but it is unable to inhibit the Gram-negative bacteria growth. | |
| Enlicitide chloride | Enlicitide chloride is an orally active inhibitor for PCSK9 that blocks the interaction between LPL receptor and PSCK9, with an IC 50 of 2.5 nM. Enlicitide chloride can be used in the study of cardiovascular diseases such as atherosclerosis, hypercholesterolemia, coronary heart disease, metabolic syndrome, acute coronary syndrome or related cardiovascular and cardiometabolic disorders [1] [2] [3]. Uses: Scientific research. Group: Peptides. Alternative Names: MK-0616 chloride. CAS No. 2407527-16-4. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-P4153. | |
| Enlimomab | Enlimomab (BI-RR 0001), a murine IgG2a monoclonal antibody to the human ICAM-1 , inhibits leukocyte adhesion to the vascular endothelium, thereby decreasing leukocyte extravasation and inflammatory tissue injury. Enlimomab has anti-inflammatory effects, and can be used for stroke research [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BI-RR 0001; Anti-Human IL6 Recombinant Antibody. CAS No. 142864-19-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99336. | |
| e-N-Maleimidocaprionate b-glucan | e-N-Maleimidocaprionate b-glucan. Product ID: 5-01205. Purity: ~2 mmol substitution. Reference: Bioconjug. Chem., 3, 132, 1992; Bioconjug. Chem., 4, 314, 1993; J. Contr. Release, 28, 155, 1994. |  |
| e-N-Maleimidocaprionate chitosan | e-N-Maleimidocaprionate chitosan. Product ID: 5-01203. Purity: ~2 mmol substitution. | |
| e-N-Maleimidocaprionate dextran | e-N-Maleimidocaprionate dextran. Product ID: 5-01204. Mole weight: Mw 40,000. Purity: ~2 mmol substitution. Reference: Bioconjug. Chem., 2, 427, 1991. | |
| e-N-Maleimidocaprionate heparin | e-N-Maleimidocaprionate heparin. Product ID: 5-01206. Purity: ~2 mmol substitution. | |
| e-N-Maleimidopropionate alginate | e-N-Maleimidopropionate alginate. Product ID: 5-01200. Purity: ~2 mmol substitution. Properties: water soluble. | |
| e-N-Maleimidopropionate carboxymethyl cellulose | e-N-Maleimidopropionate carboxymethyl cellulose. Product ID: 5-01201. Purity: ~2 mmol substitution. Reference: Bioconjug. Chem., 2, 427, 1991. | |
| e-N-Maleimidopropionate cellulose | e-N-Maleimidopropionate cellulose. Product ID: 5-01202. Purity: ~2 mmol substitution. | |
| ENMD-1198 | ENMD-1198 is an analog of 2-methoxyestradiol (2ME2) with antiproliferative and antiangiogenic activity. ENMD-1198 is a novel tubulin-binding agent that reduces HIF-1alpha and STAT3 activity in human hepatocellular carcinoma(HCC) cells. Synonyms: IRC-110160; 2-methoxyoestra-1,3,5(10),16-tetraene-3-carboxamide. Grades: 98%. CAS No. 864668-87-1. Molecular formula: C20H25NO2. Mole weight: 311.42. | |
| ENMD-2076 | ENMD-2076 is an orally-active, Aurora A/angiogenic kinase inhibitor with a unique kinase selectivity profile and multiple mechanisms of action. ENMD-2076 has been shown to inhibit a distinct profile of angiogenic tyrosine kinase targets in addition to the Aurora A kinase. Aurora kinases are key regulators of mitosis (cell division), and are often over-expressed in human cancers. ENMD-2076 also targets the VEGFR, Flt-3 and FGFR3 kinases which have been shown to play important roles in the pathology of several cancers. ENMD-2076 has shown promising activity in Phase 1 clinical trials in solid tumor cancers, leukemia, and multiple myeloma. ENMD-2076 is currently in a Phase 2 trial for ovarian cancer, and preclinical and clinical activities are ongoing in assessing the compound's applicability for other forms of cancer. Synonyms: ENMD-2076; ENMD 2076; ENMD2076. CAS No. 934353-76-1. Molecular formula: C21H25N7. Mole weight: 375.47. | |
| ENMD-2076 L-(+)-Tartaric acid | ENMD-2076 L-(+)-Tartaric acid is the tartaric acid of ENMD-2076, selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.86 nM, 25-fold more selective for Aurora A than Aurora B and less potent to VEGFR2/KDR and VEGFR3, FGFR1 and FGFR2. Synonyms: ENMD-2076 L-(+)-Tartaric acid; ENMD 2076 L-(+)-Tartaric acid; ENMD2076 L-(+)-Tartaric acid. Grades: >98%. CAS No. 1291074-87-7. Molecular formula: C25H31N7O6. Mole weight: 525.56. | |
| ENMD 547 | ENMD 547. Group: Biochemicals. Alternative Names: 6-Amino-1-[4-(3-methyl-1-oxobutyl)-1-piperazinyl]-1-hexanone hydrobromide; 1-(6-Amino-1-oxohexyl)-4-(3-methyl-1-oxobutyl)piperazine monohydrobromide. Grades: Highly Purified. CAS No. 644961-61-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C15H30BrN3O2. US Biological Life Sciences. |  Worldwide |
| Enmetazobactam | Enmetazobactam (AAI101) is an extended-spectrum β-lactamase inhibitor, against many resistant Gram-negative pathogens [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AAI101. CAS No. 1001404-83-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103095. | |
| Enniatin a | Enniatin a. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ENNIATIN A (LATERITIN I); ENNIATIN A; Enniatin-A. Product Category: Heterocyclic Organic Compound. CAS No. 2503-13-1. Molecular formula: C36H63N3O9. Mole weight: 681.9. Purity: >99%. IUPACName: (3S,9S,12R,15S,18R)-9,15-bis[(2S)-butan-2-yl]-3-[(2R)-butan-2-yl]-4,10,16-trimethyl-6,12,18-tri(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone. Canonical SMILES: CCC(C)C1C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N1C)C(C)C)C(C)CC)C)C(C)C)C(C)CC)C)C(C)C. Product ID: ACM2503131. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Enniatin A | It is produced by the strain of Fusarium orthoceras var. enniatinum. It has insecticidal and antifungal activity. Synonyms: Cyclo((2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl); N-Methylcyclo(L-Ile-D-Hmb-N-methyl-L-Ile-D-Hmb-N-methyl-L-Ile-D-Hmb-); Lateritin I. Grades: >99% by HPLC. CAS No. 2503-13-1. Molecular formula: C36H63N3O9. Mole weight: 681.90. | |
| Enniatin A1 | A family of depsipeptide ionophores, produced by several fusarium species. It has antibiotic properties. Enniatin A1 is one of four major analogues in the enniatin complex. Enniatin A1 has been found to induce apoptosis in cancer cells, decrease the activation of the cell proliferation kinase, ERK (p44/p42) and inhibit TNF-α-induced NF-κB activation. Synonyms: 2-(N-Methyl-L-valine)enniatin A; Cyclo(D-α-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-α-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-α-hydroxyisovaleryl-N-methyl-L-valyl); cyclo[N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-D-valyl]; Cyclo((2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl). Grades: >99% by HPLC. CAS No. 4530-21-6. Molecular formula: C35H61N3O9. Mole weight: 667.87. | |
| Enniatin A1 (2-(N-Methyl-L-valine) Enniatin A) | Enniatins are a family of depsipeptides produced several Fusarium species. The enniatins have been shown to act as ionophores. More recently their effects on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin A1 is one of four major analogues of the enniatin complex and has previously not been available for investigation. Group: Biochemicals. Alternative Names: 2-(N-Methyl-L-valine) Enniatin A. Grades: Highly Purified. CAS No. 4530-21-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Enniatin A (Lateritin I) | Enniatins are a family of depsipeptides produced several Fusarium species. The enniatins have been shown to act as ionophores. More recently their effects on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin A is one of four major analogs of the enniatin complex and has previously not been available for investigation. Cyclohexadepsipeptide mycotoxin. One of four major analogs in the enniatin complex. Commonly found food contaminant in cereals and their products. Ionophore antibiotic. Incorporation into the cell membrane forms dimeric structures that transport monovalent ions across the membrane (especia...:Fusarium sp. MST-FP1765. Group: Biochemicals. Alternative Names: Lateritin I; Cyclo[(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl]; N-(D-2-Hydroxy-3-methylbutyryl)-N-methyl-Isoleucine Trimol. Cyclic Ester; 1,7,13-Trioxa-4,10,16-triazacyclooctadecane Cyclic Peptide Deriv.;Cyclo(D-α-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-α-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-α-hydroxyisovaleryl-N-methyl-L-isoleucyl). Grades: Highly Purified. CAS No. 2503-13-1. Pack Sizes: 500ug. Molecular Formula: C??H??N?O?, Molecular Weight: 681.9. US Biological Life Sciences. | Worldwide |
| Enniatin B | Enniatin B is a Fusarium mycotoxin. Enniatin B inhibits acyl-CoA: cholesterol acyltransferase ( ACAT ) activity with an IC 50 of 113 μM in an enzyme assay using rat liver microsomes [1]. Enniatins B decreases the activation of ERK (p44/p42) [2]. Uses: Scientific research. Group: Natural products. CAS No. 917-13-5. Pack Sizes: 1 mg. Product ID: HY-N3806. | |
| Enniatin B | Enniatins are a complex of family produced several Fusarium species. The enniatins have been shown to act as ionophores. More recently their effects on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin B is the most studied of four major analogues of the enniatin complex. Group: Biochemicals. Grades: Highly Purified. CAS No. 917-13-5. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Enniatin B1 (2-(N-Methyl-L-isoleucine) Enniatin B) | Enniatins are a family of depsipeptides produced several Fusarium species. The enniatins have been shown to act as ionophores. More recently their effects on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin B1 is one of four major analogues of the enniatin complex and has not previously been available for investigation. Group: Biochemicals. Alternative Names: 2-(N-Methyl-L-isoleucine) Enniatin B. Grades: Highly Purified. CAS No. 19914-20-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Enniatin complex | Enniatins are a complex of depsipeptides produced by several Fusarium species. Typically, the complex contains 4 major components: A, A1, B and B1 together with minor amounts of enniatin C, D, E and F. The enniatins have been shown to act as ionophores. Recently, their effects on acyl-CoA cholesterol transferase, as nematocides and the selectivity of their antitumor action have received more focus. Group: Biochemicals. Grades: Highly Purified. CAS No. 11113-62-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Enniatin complex | A complex of depsipeptides produced by several fusarium species. the complex contains 4 major components: A, A1, B and B1 together with minor amounts of enniatins C, D, E and F. Synonyms: cyclo[N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-isoleucyl-N-oxa-D-valyl] compound with cyclo[N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-L-valyl] compound with cyclo[N-methyl-L-isoleucyl-N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-D-valyl] compound with cyclo[N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-D-valyl-N-methyl-L-valyl-N-oxa-D-valyl-N-methyl-L-valyl]. Grades: >95% by HPLC. CAS No. 11113-62-5. Molecular formula: C36H63N3O9. C35H61N3O9. C34H59N3O9. C33H57N3O9. Mole weight: 2643.46. | |
| Enniatin F | It is produced by the strain of Fusarium orthoceras var. enniatinum. It has insecticidal and antifungal activity, and it also can inhibit Acylcoa, cholesterol acyltransferase (ACAT). Synonyms: Enniatin A, 2-(N-methyl-L-leucine)-; Cyclo(hiv-Me-leu-hiv-Me-ile-hiv-Me-ile). CAS No. 144446-20-8. Molecular formula: C36H63N3O9. Mole weight: 681.90. | |
| Enoblituzumab | Enoblituzumab (MGA271) is a humanized IgG1κ monoclonal antibody recognizing human B7-H3 protein, a member of the B7 family of immune regulators [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MGA271. CAS No. 1353485-38-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9966. | |
| Enocitabine | Enocitabine. Group: Biochemicals. Grades: Highly Purified. CAS No. 55726-47-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C31H55N3O6. US Biological Life Sciences. | Worldwide |
| Enocitabine (N- (1-B-D-Arabinofuranosyl-1, 2-dihydro-2-oxo-4-pyrimidinyl) docosanamide, Behenoylcytosine Arabinoside, BH-AC, NSC-239336, Sunrabin) | An antineoplastic. A derivative of Cytarabine. Group: Biochemicals. Alternative Names: N- (1-B-D-Arabinofuranosyl-1, 2-dihydro-2-oxo-4-pyrimidinyl) docosanamide, Behenoylcytosine Arabinoside, BH-AC, NSC-239336, Sunrabin. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Enocyanin | Enocyanin. Synonyms: GRAPE SKIN EXTRACT 30% POLYPHENOLS;Anthocyanins, grape; BLUEBERRYANTHOCYANINS; GRAPEJUICECOLOUR; HIBISCUSSABDARIFFAL.ANTHOCYANINS; GRAPESKINCOLOUR; PURPLECORNCOLOUR; TAMARINDCOLOUR. CAS No. 11029-12-2. Pack Sizes: 1 kg. Product ID: CDF4-0026. Molecular formula: C15H11O+. Category: Color Fixative. Product Keywords: Food Ingredients; Color Fixative; Enocyanin; CDF4-0026; 11029-12-2; C15H11O+; 11029-12-2. Purity: 0.99. Color: Very Dark Purple to Black. Physical State: Solid. Solubility: DMF (Slightly), DMSO (Slightly), Methanol (Slightly). Storage: -20°C. |  |
| Enokizumab | Enokizumab is a monoclonal antibody targeting interleukin-9. Synonyms: MEDI-528; MEDI 528; MEDI528. CAS No. 909875-08-7. | |
| Enokizumab | Enokizumab (MEDI-528) is a monoclonal antibody targeting to interleukin (IL)-9. IL-9 regulates the development of airway inflammation, mucus production, airway hyperresponsiveness, and airway fibrosis largely by increasing mast cell numbers and activity in the airways [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MEDI-528. CAS No. 909875-08-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99193. | |
| Enopeptin A | It is produced by the strain of Streptomyces griseus. It has activity against gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), and it also has antibacterial activity of phage. Synonyms: N-[[(2E,4E,6E,8E,10E)-12-(2-Hydroxy-5-oxo-1-cyclopentenylamino)-1,12-dioxo-2,4,6,8,10-dodecapentenyl]-L-Phe-]cyclo[L-Ser*-L-Pro-N-methyl-L-Ala-L-Ala-4β-methyl-L-Pro-]; [trans-(all-E)]-1-[N-[N-[1-[N-[N-[12-[(2-Hydroxy-5-oxo-1-cyclopenten-1-yl)amino]-1,12-dioxo-2,4,6,8,10-dodecapentaenyl]-L-phenylalanyl]-L-seryl]-L-prolyl]-N-methyl-L-alanyl]-L-alanyl]-4-methyl-L-proline ξ-lactone; Enopeptin II; NSC657143. Grades: >95% by HPLC. CAS No. 139601-96-0. Molecular formula: C47H57N7O11. Mole weight: 896.00. | |
| Enoticumab | Enoticumab (REGN421, SAR153192) is an IgG1κ antibody targeting human Dll4. DLL4 is a ligand of the Notch signaling pathway and regulates fatty acid uptake through non-transcriptional regulation of macropinocytosis-dependent long-chain fatty acid uptake. Specific in vivo activity of Enoticumab in an ovarian xenograft model. EGN421 (2.5 mg/kg once weekly) resulted in 86% and 83% tumor growth inhibition in mouse subcutaneous TOV-112D or intraperitoneal A2780 human tumor xenograft models, respectively [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: REGN421. CAS No. 1192578-27-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99925. | |
| Enoxacin | A fluororquinolone antibacterial used to treat urinary tract infections and gonorrhea. Group: Biochemicals. Alternative Names: 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid; Enofloxacin; Enofloxacine; Enoksetin; Flumark; NSC 629661; PD 107779; Penetrex. Grades: Highly Purified. CAS No. 74011-58-8. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Enoxacin | Enoxacin is an oral broad-spectrum fluoroquinolone antibacterial agent used in the treatment of urinary tract infections and gonorrhea. Insomnia is a common adverse effect. Uses: Anti-bacterial agents. Synonyms: R41468; R41468; R-41468; PD 107779; PD-107779; PD107779; Penetrex; Enoxacine; Comprecin. Grades: >98%. CAS No. 74011-58-8. Molecular formula: C15H17FN4O3. Mole weight: 320.32. | |
| Enoxacin | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C15H17FN4O3. CAS No. 74011-58-8. Prepack ID 71188914-1g. Molecular Weight 320.32. See USA prepack pricing. |  |
| Enoxacin hydrate | Enoxacin hydrate (Enoxacin sesquihydrate), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC 50 =126 μg/ml) and topoisomerase IV (IC 50 =26.5 μg/ml). Enoxacin hydrate is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin hydrate has potent activities against gram-positive and -negative bacteria. Enoxacin hydrate is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Enoxacin sesquihydrate; AT-2266 hydrate; CI-919 hydrate. CAS No. 84294-96-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0268A. | |
| Enoxacin hydrate | Enoxacin hydrate is a synthetic antibiotic belonging to quinolone carboxylic acid compound. It is bactericidal and has a postantibiotischen effect. It is a broad-spectrum antibacterial agent and inhibited 90% Escherichia coli, Klebsiella sp., Aeromonas sp., Enterobacter spp., Serratia spp., Proteus mirabilis, and Morganella morganii at less than or equal to 0.8 micrograms/ml. Uses: Enoxacin hydrate is bactericidal and has a postantibiotischen effect. it is a broad-spectrum antibacterial agent. Synonyms: Enoxacin sesquihydrate;AT-2266 hydrate;CI-919 hydrate; AT 2266 hydrate;CI 919 hydrate; AT2266 hydrate;CI919 hydrate; 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid hydrate. Grades: >98%. CAS No. 84294-96-2. Molecular formula: C30H40F2N8O9. Mole weight: 694.694. | |
| Enoxacin Sesquihydrate | Enoxacin Sesquihydrate. Group: Biochemicals. Alternative Names: 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic Acid Sesquihydrate. Grades: Highly Purified. CAS No. 84294-96-2. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Enoxaparin | Enoxaparin (PK 10169), a low-molecular-weight heparin (LMWH) derivative. Enoxaparin exerts anticoagulant activity through antithrombin III, an endogenous inhibitor of factor Xa and thrombin IIa. Enoxaparin protect the rat hippocampus against TBI (traumatic brain injury) via antioxidant and anti-inflammatory properties. Enoxaparin can be used for the research of deep vein thrombosis (DVT), pulmonary embolism, TBI and COVID-19 [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PK 10169; Enoxaparin sodium. CAS No. 679809-58-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109509. | |
| Enoxaparin sodium | Cas No. 679809-58-6. | |
| Enoxaparin Sodium | Enoxaparin Sodium. Group: Biochemicals. Alternative Names: Heparin sodium salt. Grades: Purified. CAS No. 679809-58-6. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: (C25H40N2O36S5)n Polymer, Molecular Weight (ave): 3500-5500. US Biological Life Sciences. | Worldwide |
| Enoxaparin Sodium | Enoxaparin sodium consists of a complex set of oligosaccharides that have not yet been fully characterized. Most of the components have a 4-chenuronic acid structure at the non-reducing end of their chains. About 20% of the materials containing Chemicalbook have 1, 6-dehydrated derivatives at the reduced end of the chain, ranging between 15% and 25%. The weight average molecular weight of sodium Enox-aparin is 4500Da and ranges from 3800 to 5000Da. Synonyms: ENOXAPARIN SODIUM, EP STANDARD;Lovenox;Lovenox (preservative free); Unii-8nz41mik1o; Clexane; Enoxil; Klexane; Enoxaparin SodiuM EP. CAS No. 679809-58-6. Product ID: PAP-0073. Molecular formula: C57H82N4Na4O53S3. Category: Cardiovascular. Product Keywords: Cardiovascular Series; Enoxaparin Sodium; PAP-0073; Cardiovascular; C57H82N4Na4O53S3; 679809-58-6. Appearance: White to Off-White. Standard: CP/EP/USP. Chemical Name: ENOXAPARIN SODIUM, EP STANDARD;Lovenox;Lovenox (preservative free); Unii-8nz41mik1o; Clexane; Enoxil; Klexane; Enoxaparin SodiuM EP. Grade: Pharmaceutical Grade. Solubility: Water (Slightly). Storage: Room Temperature, Under inert atmosphere. Product Description: Enoxaparin sodium consists of a complex set of oligosaccharides that have not yet been fully characterized. Most of the components have a 4-chenuronic acid structure at the non-reducing end of their chains. About 20% of the materials containing Chemicalbook have 1, 6-dehydrated derivatives at t | |
| Enoxaparin Sodium EP | low-molecular-mass heparin. Grades: EP. CAS No. 679809-58-6. Product ID: 4-00670. Mole weight: Mw 3800-5000. Purity: > 90 - 125 IU of anti-factor Xa activity/mg, ratio of anti-factor Xa activity to anti-factor IIa activity 3.3 - 5.3. Properties: degree of sulphation is about 2 per disaccharide unit. Source : obtained by nitrous acid depolymerisation of heparin from pork intestinal mucosa, followed by fractionation to eliminate selectively most of the chains with a molecular mass below 2000. | |
| Enoxastrobin | Enoxastrobin is a fungicide. Group: Biochemicals. Grades: Highly Purified. CAS No. 238410-11-2. Pack Sizes: 10mg, 25mg. Molecular Formula: C22H22ClNO4, Molecular Weight: 399.87. US Biological Life Sciences. | Worldwide |
| Enoximone | Enoximone is a selective phosphodiesterase III (PDE3) inhibitor. It can be used for the treatment of heart failure. Uses: Heart failure. Synonyms: Enoximone; Perfan; Fenoximone; MDL-17043; Enoximonum [Latin]; MDL 19438; MDL-17,043; MDL-17043; MDL-19,438; MDL17,043; MDL17043; MDL19,438; Myogen Brand of Enoximone; Perfan; 1,3-Dihydro-4-methyl-5-[4-(methylthio)benzoyl]-2H-imidazol-2-one; Fenoximone; MDL 17043; Perfan; Perfane; RMI 17043. Grades: 98%. CAS No. 77671-31-9. Molecular formula: C12H12N2O2S. Mole weight: 248.3. | |
| Enoximone | Enoximone is an inotropic vasodilating agent and a selective and orally active phosphodiesterase III (PDE3) inhibitor with an IC 50 of 5.9 μM. Enoximone induces vasodilatation and increases intracellular levels of cAMP by inhibiting cGMP-inhibited PDE. Enoximone also exhibits PDE4 inhibitory effect with an IC 50 of 21.1 μM for myocardial PDE4A. Enoximone has the potential for congestive heart failure research and has bronchodilatory, antiasthma and anti-inflammatory effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77671-31-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1639. | |
| Enoximone | Enoximone. Group: Biochemicals. Grades: Purified. CAS No. 77671-31-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| enoyl-[acyl-carrier-protein] reductase (NADH) | The enzyme catalyses an essential step in fatty acid biosynthesis, the reduction of the 2,3-double bond in enoyl-acyl-[acyl-carrier-protein] derivatives of the elongating fatty acid moiety. The enzyme from the bacterium Escherichia coli accepts substrates with carbon chain length from 4 to 18. The enzyme from the bacterium Mycobacterium tuberculosis prefers substrates with carbon chain length from 12 to 24 carbons. Group: Enzymes. Synonyms: enoyl-[acyl carrier protein] reductase; enoyl-ACP reductase; NADH-enoyl acyl carrier protein reductase; NADH-specific enoyl-ACP reductase; acyl-[acyl-carrier-protein]:NAD+ oxidoreductase; fabI (gene name); inhA (gene name). Enzyme Commission Number: EC 1.3.1.9. CAS No. 37251-08-4. 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-1359; enoyl-[acyl-carrier-protein] reductase (NADH); EC 1.3.1.9; 37251-08-4; enoyl-[acyl carrier protein] reductase; enoyl-ACP reductase; NADH-enoyl acyl carrier protein reductase; NADH-specific enoyl-ACP reductase; acyl-[acyl-carrier-protein]:NAD+ oxidoreductase; fabI (gene name); inhA (gene name). Cat No: EXWM-1359. |  |
| enoyl-[acyl-carrier-protein] reductase (NADPH) | The enzyme completes each cycle of fatty acid elongation by catalysing the stereospecific reduction of the double bond at position 2 of a growing fatty acid chain, while linked to the acyl-carrier protein, in an NADPH-dependent manner. This entry stands for enzymes whose stereo-specificity with respect to NADP+ is not known. [cf. EC 1.3.1.39 enoyl-[acyl-carrier-protein] reductase (NADPH, Re-specific), EC 1.3.1.10, enoyl-[acyl-carrier-protein] reductase (NADPH, Si-specific) and EC 1.3.1.9, enoyl-[acyl-carrier-protein] reductase (NADH)]. Group: Enzymes. Synonyms: acyl-ACP dehydrogenase (ambiguous); enoyl-[acyl carrier protein] (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADPH 2-enoyl Co A reductase; enoyl-ACP reductase (ambiguous); fabL (gene name). Enzyme Commission Number: EC 1.3.1.104. 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-1276; enoyl-[acyl-carrier-protein] reductase (NADPH); EC 1.3.1.104; acyl-ACP dehydrogenase (ambiguous); enoyl-[acyl carrier protein] (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADPH 2-enoyl Co A reductase; enoyl-ACP reductase (ambiguous); fabL (gene name). Cat No: EXWM-1276. | |
| enoyl-[acyl-carrier-protein] reductase (NADPH, Re-specific) | This enzyme completes each cycle of fatty acid elongation by catalysing the stereospecific reduction of the double bond at position 2 of a growing fatty acid chain, while linked to an acyl-carrier protein. It is one of the activities of EC 2.3.1.85, animal fatty-acid synthase. The mammalian enzyme is Re-specific with respect to NADP+. cf. EC 1.3.1.10, enoyl-[acyl-carrier-protein] reductase (NADPH, Si-specific) and EC 1.3.1.104, enoyl-[acyl-carrier-protein] reductase (NADPH). Group: Enzymes. Synonyms: acyl-ACP dehydrogenase; enoyl-[acyl carrier protein] (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADPH 2-enoyl Co A reductase. Enzyme Commission Number: EC 1.3.1.39. 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-1311; enoyl-[acyl-carrier-protein] reductase (NADPH, Re-specific); EC 1.3.1.39; acyl-ACP dehydrogenase; enoyl-[acyl carrier protein] (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADPH 2-enoyl Co A reductase; enoyl-ACp reductase; enoyl-[acyl-carrier-protein] reductase (NADPH2, A-specific); acyl-[acyl-carrier-protein]:NADP+ oxidoreductase (A-specific); enoyl-[acyl-carrier-protein] reductase (NADPH, A-specific); acyl-[acyl-carrier protein]:NADP+ oxidoreductase (A-specific). Cat No: EXWM-1311. | |
| enoyl-[acyl-carrier-protein] reductase (NADPH, Si-specific) | One of the activities of EC 2.3.1.86, fatty-acyl-CoA synthase, an enzyme found in yeasts (Ascomycota and the Basidiomycota). Catalyses the reduction of enoyl-acyl-[acyl-carrier protein] derivatives of carbon chain length from 4 to 16. The yeast enzyme is Si-specific with respect to NADP+. cf. EC 1.3.1.39, enoyl-[acyl-carrier-protein] reductase (NADPH, Re-specific) and EC 1.3.1.104, enoyl-[acyl-carrier-protein] reductase (NADPH), which describes enzymes whose stereo-specificity towards NADPH is not known. See also EC 1.3.1.9, enoyl-[acyl-carrier-protein] reductase (NADH). Group: Enzymes. Synonyms: acy. Enzyme Commission Number: EC 1.3.1.10. CAS No. 37251-09-5. 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-1271; enoyl-[acyl-carrier-protein] reductase (NADPH, Si-specific); EC 1.3.1.10; 37251-09-5; acyl-ACP dehydrogenase (ambiguous); enoyl-[acyl carrier protein] (reduced nicotinamide adenine dinucleotide phosphate) reductase; NADPH 2-enoyl Co A reductase; enoyl acyl-carrier-protein reductase (ambiguous); enoyl-ACP reductase (ambiguous); acyl-[acyl-carrier-protein]:NADP+ oxidoreductase (B-specific); acyl-[acyl-carrier protein]:NADP+ oxidoreductase (B-specific); enoyl-[acyl-carrier-protein] reductase (NADPH, B-specific). Cat No: EXWM-1271. | |
| enoyl-CoA hydratase | Acts in the reverse direction. With cis-compounds, yields (3R)-3-hydroxyacyl-CoA. cf. EC 4.2.1.74 long-chain-enoyl-CoA hydratase. Group: Enzymes. Synonyms: enoyl hydrase; unsaturated acyl-CoA hydratase; β-hydroxyacyl-CoA dehydrase; β-hydroxyacid dehydrase; acyl coenzyme A hydrase; crotonase; crotonyl hydrase; 2-octenoyl coenzyme A hydrase; enoyl coenzyme A hydratase; 2-enoyl-CoA hydratase; short-chain enoyl-CoA hydratase; ECH; trans-2-enoyl-CoA hydratase; enoyl coenzyme A hydrase (D); enoyl coenzyme A hydrase (L); short chain enoyl coenzyme A hydratase; D-3-hydroxyacyl-CoA dehydratase; enol-CoA hydratase. Enzyme Commission Number: EC 4.2.1.17. CAS No. 9027-13-8. 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-5010; enoyl-CoA hydratase; EC 4.2.1.17; 9027-13-8; enoyl hydrase; unsaturated acyl-CoA hydratase; β-hydroxyacyl-CoA dehydrase; β-hydroxyacid dehydrase; acyl coenzyme A hydrase; crotonase; crotonyl hydrase; 2-octenoyl coenzyme A hydrase; enoyl coenzyme A hydratase; 2-enoyl-CoA hydratase; short-chain enoyl-CoA hydratase; ECH; trans-2-enoyl-CoA hydratase; enoyl coenzyme A hydrase (D); enoyl coenzyme A hydrase (L); short chain enoyl coenzyme A hydratase; D-3-hydroxyacyl-CoA dehydratase; enol-CoA hydratase. Cat No: EXWM-5010. | |
| enoyl-CoA hydratase 2 | This enzyme catalyses a hydration step in peroxisomal β-oxidation. The human multifunctional enzyme type 2 (MFE-2) is a 79000 Da enzyme composed of three functional units: (3R)-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase 2 and sterol carrier protein 2-like units. The enzymes from Aeromonas caviae and Arabidopsis thaliana are monofunctional enzymes. 2-Enoyl-CoA hydratase 3 from Candida tropicalis is a part from multifunctional enzyme type 2. Group: Enzymes. Synonyms: 2-enoyl-CoA hydratase 2; AtECH2; ECH2; MaoC; MFE-2; PhaJAc; D-3-hydroxyacyl-CoA hydro-lyase; D-specific 2-trans-enoyl-CoA hydratase. Enzyme Commission Number: EC 4.2.1.119. 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-4959; enoyl-CoA hydratase 2; EC 4.2.1.119; 2-enoyl-CoA hydratase 2; AtECH2; ECH2; MaoC; MFE-2; PhaJAc; D-3-hydroxyacyl-CoA hydro-lyase; D-specific 2-trans-enoyl-CoA hydratase. Cat No: EXWM-4959. | |
| Enpatoran free base | Enpatoran, also known as M5049, is a novel selective Toll-Like Receptor 7/8 Inhibitor for Treatment of Autoimmunity. M5049 was found to be potent in vivo as TLR7/8 inhibition efficaciously treated disease in several murine lupus models and, interestingly, was efficacious in a disease context in which TLR7/8 activity has not previously been considered a primary disease driver. Furthermore, M5049 had greater potency in disease models than expected based on its in vitro potency and pharmacokinetic/pharmacodynamic properties. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Enpatoran; M 5049; M5049; M-5049. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 2101938-42-3. Molecular formula: C16H15F3N4. Mole weight: 320.32. Purity: >98%. IUPACName: 5-((3R,5S)-3-amino-5-(trifluoromethyl)piperidin-1-yl)quinoline-8-carbonitrile. Canonical SMILES: N[C@]1([H])C[C@]([H])(C(F)(F)F)CN(C2=CC=C(C#N)C3=C2C=CC=N3)C1. Product ID: ACM2101938423. Alfa Chemistry ISO 9001:2015 Certified. | |
| Enprofylline | Enprofylline acts as a selective and competitive A2B receptor antagonist with the K i of 7 μM. Enprofylline also acts as a phosphodiesterase inhibitor. Enprofylline can be used for the research of asthma, chronic obstructive pulmonary disease [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 41078-02-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-14117. | |
| Enprofylline | Enprofylline, a xanthine derivative, is a a competitive nonselective phosphodiesterase inhibitor with relatively little activity as a nonselective adenosine receptor antagonist used in the treatment of asthma, which acts as a bronchodilator. Uses: Nonselective adenosine receptor antagonist. Synonyms: 3-Propylxanthine; 3-propyl-7H-purine-2,6-dione. Grades: ≥98%. CAS No. 41078-02-8. Molecular formula: C8H10N4O2. Mole weight: 194.19. | |
| Enrasentan | Enrasentan, an indene derivative, has been found to be an endothelin receptor antagonist that was once studied in reperfusion injury and heart failure therapy. Synonyms: Enrasentan; SB-217242; UNII-QG16H8A6ZH; SB 217242; SB217242; CHEMBL431651; (1S,2R,3S)-1-(1,3-benzodioxol-5-yl)-3-[2-(2-hydroxyethoxy)-4-methoxyphenyl]-5-propoxy-2,3-dihydro-1H-indene-2-carboxylic acid. Grades: 98%. CAS No. 167256-08-8. Molecular formula: C29H30O8. Mole weight: 506.55. | |
| Enrofloxacin | Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL forMycoplasma bovis. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-quinoline-3-carboxylic acid; Baytri; Enrofloxacin; ROFLOXACIN BASE; Enrofoxacin; Enrolfoxacin; bayvp2674; 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-3-quinolinecarboxylic acid; 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethylpiperazino)-quinoline-3-carboxylic acid; 1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid; 1-cyclopropyl-7-(4-ethyl-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid; Enorfloxacin; cfpq. Product Category: Inhibitors. Appearance: Pale Yellow Crystals. CAS No. 93106-60-6. Molecular formula: C19H22FN3O3. Mole weight: 359.39. Purity: 95%+. IUPACName: 1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxoquinoline-3-carboxylicacid. Canonical SMILES: CCN1CCN(CC1)C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4CC4)F. Density: 1.385g/cm³. ECNumber: 618-911-2. Product ID: ACM93106606. Alfa Chemistry ISO 9001:2015 Certified. | |
| Enrofloxacin | Fluorinated quinolone antibacterial. Group: Biochemicals. Alternative Names: 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid; CFPQ; Bay vp 2674. Grades: Highly Purified. CAS No. 93106-60-6. Pack Sizes: 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Enrofloxacin | Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC 90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Group: Natural products. Alternative Names: BAY Vp 2674; PD160788. CAS No. 93106-60-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0502. | |
| Enrofloxacin | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C19H22FN3O3. CAS No. 93106-60-6. Prepack ID 57134695-5g. Molecular Weight 359.39. See USA prepack pricing. | |
| Enrofloxacin Base | Enrofloxacin Base. Categories: enrofloxacin; 93106-60-6. |  CA, FL & NJ |
| Enrofloxacin-d5 | Enrofloxacin-d 5 is the deuterium labeled Enrofloxacin. Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: BAY Vp 2674-d5; PD160788-d5. CAS No. 1173021-92-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0502S. | |
| Enrofloxacin-d5 | Labeled fluorinated quinolone antibacterial. Group: Biochemicals. Alternative Names: 1-Cyclopropyl-7-[4-(ethyl-d5)-1-piperazinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid; CFPQ-d5; Bay Vp 2674-d5; Baytril-d5. Grades: Highly Purified. CAS No. 1173021-92-5. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Enrofloxacin EP Impurity E | Enrofloxacin EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 6-chloro-1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. CAS No. 1369495-59-9. Molecular Formula: C19H22ClN3O3. Mole Weight: 375.85. Catalog: APB1369495599. |  |
Our database is helping our users find suppliers everyday.
