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| Product | Description | |
|---|---|---|
| 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. Alternative Names: ENMD-2076; ENMD 2076; ENMD2076. CAS No. 934353-76-1. Molecular formula: C21H25N7. Mole weight: 375.47. |  |
| 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 |
| Enmein | Enmein is a natural diterpenoid compound found in several plants. Alternative Names: Isodonin. Grades: >98%. CAS No. 3776-39-4. Molecular formula: C20H26O6. Mole weight: 362.42. | |
| Enmein | Enmein is isolated from I. serra with immunosuppressive effect[1]. Uses: Scientific research. Category: Natural products. CAS No. 3776-39-4. Pack Sizes: 1 mg. Product ID: HY-N5028. |  |
| Enmetazobactam | Enmetazobactam (AAI101) is an extended-spectrum β-lactamase inhibitor, against many resistant Gram-negative pathogens[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AAI101. CAS No. 1001404-83-6. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-103095. | |
| Enniatin A | It is produced by the strain of Fusarium orthoceras var. enniatinum. It has insecticidal and antifungal activity. Alternative Names: 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. Alternative Names: 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 | 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 B | It is produced by the strain of Fusarium orthoceras var. enniatinum. It has insecticidal and antifungal activity. Uses: Anti-bacterial agents. Alternative Names: 3-N-Methylvaline Enniatin; Cyclo[(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl]; Cyclo(3-methyl-D-2-hydroxybutanoyl-N-methyl-L-valyl-3-methyl-D-2-hydroxybutanoyl-N-methyl-L-valyl-3-methyl-D-2-hydroxybutanoyl-N-methyl-L-valyl). Grades: >99% by HPLC. CAS No. 917-13-5. Molecular formula: C33H57N3O9. Mole weight: 639.82. | |
| Enniatin B1 | A family of depsipeptide ionophores, produced by several fusarium species. It has antibiotic properties. It is a cytotoxic and insecticidal agent. Alternative Names: 2-(N-Methyl-L-isoleucine)enniatin B; Cyclo[(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-isoleucyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl-(2R)-2-hydroxy-3-methylbutanoyl-N-methyl-L-valyl]; 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]. Grades: >99% by HPLC. CAS No. 19914-20-6. Molecular formula: C34H59N3O9. Mole weight: 653.85. | |
| Enniatin B1 | Enniatin B1 is a Fusarium mycotoxin. Enniatin B1 inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 73 μM in an enzyme assay using rat liver microsomes[1]. Enniatin B1 crosss the blood-brain barrier[2]. Enniatin B1 decreases the activation of ERK (p44/p42). Enniatin B1 inhibits moderately TNF-α-induced NF-κB activation[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 19914-20-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N3807. | |
| 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. Alternative Names: 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). Alternative Names: 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. Category: Signaling pathways. 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 |
| 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 (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. Category: Signaling pathways. 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. Alternative Names: 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. Category: Signaling pathways. Alternative Names: REGN421. CAS No. 1192578-27-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99925. | |
| 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 | 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 (NSC-629661) is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent (fluoroquinolones) structurally related to nalidixic acid. Category: Active pharmaceutical ingredients. CAS No. 74011-58-8. Product ID: API74011588. Molecular formula: C15H17FN4O3. Mole weight: 320.32. |  |
| 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. Alternative Names: 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 hydrate | Enoxacin hydrate (AT-2266 hydrate) is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent. Category: Active pharmaceutical ingredients. CAS No. 84294-96-2. Product ID: API84294962. Molecular formula: C15H17FN4O3·3/2H2O. Mole weight: 347.34. | |
| 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. Category: 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 | Enoxaparin sodium is an anticoagulant medication used for the prevention of blood clots such as deep vein thrombosis (DVT), and also for the treatment of blood vessel complications in patients with angina and heart attack. CAS No. 679809-58-6. | |
| 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 | 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 |
| 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. Group: Biochemicals. Grades: Purified. CAS No. 77671-31-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Enoximone | Enoximone is an inotropic vasodilating agent and a selective and orally active phosphodiesterase III (PDE3) inhibitor with an IC50 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 IC50 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. Category: Signaling pathways. CAS No. 77671-31-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-B1639. | |
| 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 | Enpatoran (M5049) is a potent, orally active and dual TLR7/8 inhibitor with IC50s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran is inactive against TLR3, TLR4 and TLR9. Enpatoran can block molecule synthetic ligands and natural endogenous RNA ligands. Enpatoran exhibits excellent pharmacokinetic properties in vivo. Enpatoran can be used for both innate and adaptive autoimmunity blocking research [1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: M5049. CAS No. 2101938-42-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-134581. | |
| Enpatoran | Enpatoran is a potent and orally active dual inhibitor of TLR7/8 with IC50s of 11.1 and 24.1 nM in HEK293 cells, respectively. It blocks molecule synthetic ligands and natural endogenous RNA ligands. It has good pharmacokinetic properties in vivo and can be used to study innate and adaptive autoimmune blocks. Alternative Names: 8-Quinolinecarbonitrile, 5-[(3R,5S)-3-amino-5-(trifluoromethyl)-1-piperidinyl]-; 5-[(3R,5S)-3-Amino-5-(trifluoromethyl)-1-piperidinyl]-8-quinolinecarbonitrile; 5-((3R,5S)-3-Amino-5-trifluoromethylpiperidin-1-yl)quinoline-8-carbonitrile; M 5049; M5049; M-5049. Grades: ≥95%. CAS No. 2101938-42-3. Molecular formula: C16H15F3N4. Mole weight: 320.31. | |
| Enpatoran hydrochloride | Enpatoran (M5049) hydrochloride is a potent, orally active and dual TLR7/8 inhibitor with IC50s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran hydrochloride is inactive against TLR3, TLR4 and TLR9. Enpatoran hydrochloride can block molecule synthetic ligands and natural endogenous RNA ligands. Enpatoran hydrochloride exhibits excellent pharmacokinetic properties in vivo. Enpatoran hydrochloride can be used for both innate and adaptive autoimmunity blocking research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: M5049 hydrochloride. CAS No. 2101945-93-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-134581A. | |
| Enpp-1-IN-1 | Enpp-1-IN-1 is an effective selective enpp-1 (nucleotide pyrophosphatase-phosphodiesterase 1) inhibitor[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2289728-58-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129490. | |
| Enpp-1-IN-14 | Enpp-1-IN-14 (Compound 015) is a potent Ectonucleotide Pyrophosphatase/Phosphodiesterase-1 (ENPP1) inhibitor with an IC50 value of 32.38 nM for recombinant human ENPP-1. Enpp-1-IN-14 has anti-tumor activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2687222-59-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147389. | |
| Enpp-1-IN-2 | Enpp-1-IN-2 (Compound C) is a potent ENPP1 (ectonucleotide pyrophosphatase/phosphodiesterase 1) inhibitor with IC50 values of 0.26, 0.48 and 2.0 μM evaluated by means of TG-mAMP, pNP-TMP, and ATP assays, respectively. TG (Tokyo Green)-mAMP: a newly synthesized sensitive ENPP1 fluorescence probe[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2378640-92-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139362. | |
| ENPP3 Inhibitor 1 | ENPP3 Inhibitor 1 is a selective inhibitor of ENPP3, with IC50s of 0.15 μM (ENPP3) and 41.4 μM (ENPP1) respectively. ENPP3 Inhibitor 1 shows anti-tumor activities against breast cancer and cervical cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2803505-90-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-169804. | |
| Enramycin | Enramycin. Alternative Names: Enramicina; Enramycinum; Enramycin[INN]; Enramycinum[INN-Latin]; Enramicina[INN-Spanish]; 12772-37-1. Grades: 95%. CAS No. 12772-37-1. Molecular formula: C107H140Cl2N26O32. Mole weight: 2373.3175. | |
| Enristomig | Enristomig (ES-101) is a multispecific antibody. Enristomig is both a PD-L1 antagonist and a conditional agonist of 4-1BB. Enristomig can be used for research on PD-L1 expressing tumors[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ES-101; INBRX-105. CAS No. 2539845-73-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P990738. | |
| Enrofloxacin | Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Uses: Scientific research. Category: Induced disease models products. Alternative Names: BAY Vp 2674; PD160788. CAS No. 93106-60-6. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 5 g; 10 g. Product ID: HY-B0502. | |
| 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 is a fluoroquinolone antibiotic that prevents DNA superhelix and DNA synthesis by inhibiting bacterial DNA gyrase (a type II topoisomerase). It can be used for bacterial diseases caused by sensitive bacteria in livestock and small animals. Alternative Names: Baytril; Enrofloxacine; CFPQ; Enrofloxacino; Bay Vp 2674. Grades: >98%. CAS No. 93106-60-6. Molecular formula: C19H22FN3O3. Mole weight: 359.39. | |
| 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-d5 is intended for use as an internal standard for the quantification of enrofloxacin by GC- or LC-MS. Category: Active pharmaceutical ingredients. CAS No. 1173021-92-5. Product ID: API1173021925. Molecular formula: C19H17D5FN3O3. Mole weight: 364.43. | |
| 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-[d5] | Enrofloxacin-[d5] is the labelled analogue of Enrofloxacin, which is a fluoroquinolone antibiotic. Enrofloxacin is used in the treatment of individual pets and domestic animals. Alternative Names: Enrofloxacin D5; 1-Cyclopropyl-7-[4-(ethyl-d5)-1-piperazinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid; CFPQ-d5; Baytril-d5. Grades: ≥99%; ≥99% atom D. CAS No. 1173021-92-5. Molecular formula: C19H17D5FN3O3. Mole weight: 364.43. | |
| Enrofloxacin EP Impurity E | Enrofloxacin EP Impurity E. Uses: For analytical and research use. 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. |  |
| Enrofloxacin EP Impurity F | Enrofloxacin EP Impurity F. Uses: For analytical and research use. Alternative Names: 1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoroquinolin-4(1H)-one. CAS No. 131775-99-0. Molecular formula: C18H22FN3O. Mole weight: 315.39. Catalog: APB131775990. | |
| Enrofloxacin hydrochloride | Enrofloxacin hydrochloride is a fluoroquinolone antibiotic commonly used in veterinary medicine. Alternative Names: Enrofloxacin HCl. CAS No. 112732-17-9. Molecular formula: C19H22FN3O3.HCl. Mole weight: 395.86. | |
| Enrofloxacin hydrochloride | Enrofloxacin hydrochloride. CAS No. 112732-17-9. Product ID: ACM112732179. Molecular formula: C19H22FN3O3?HCl. Mole weight: 395.86. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Enrofloxacin hydrochloride | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C19H22FN3O3 ¢HCl. CAS No. 112732-17-9. Prepack ID 89967261-1g. Molecular Weight 395.86. See USA prepack pricing. | |
| Enrofloxacin monohydrochloride | Enrofloxacin monohydrochloride (BAY Vp 2674 monohydrochloride) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis. Enrofloxacin monohydrochloride shows inhibitory activity against vaccinia virus (VV). Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY Vp 2674 monohydrochloride; PD160788 monohydrochloride. CAS No. 93106-59-3. Pack Sizes: 10 mM * 1 mL in Water; 500 mg; 5 g; 10 g. Product ID: HY-B0502A. | |
| Enrofloxacin monohydrochloride | Enrofloxacin monohydrochloride (BAY Vp 2674 monohydrochloride) is a potent antibiotic with a minimum inhibitory concentration (MIC 90) of 0.312 μg/mL against Mycoplasma bovis, and it also exhibits inhibitory activity against the vaccinia virus (VV). Category: Active pharmaceutical ingredients. CAS No. 93106-59-3. Product ID: API93106593. Molecular formula: C19H23ClFN3O3. Mole weight: 395.86. | |
| Ensartinib | Ensartinib (X-396) is a potent dual ALK/MET inhibitor with IC50 values of. Category: Active pharmaceutical ingredients. CAS No. 1370651-20-9. Product ID: API1370651209. Molecular formula: C26H27Cl2FN6O3. Mole weight: 561.44. | |
| Ensartinib | Ensartinib (X-396) is a BBB-permeable and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: X-396. CAS No. 1370651-20-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103714. | |
| Ensartinib dihydrochloride | Ensartinib dihydrochloride (X-396 dihydrochloride) is a BBB-permeable and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: X-396 dihydrochloride. CAS No. 2137030-98-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103714A. | |
| Ensartinib hydrochloride | Ensartinib hydrochloride (X-396 dihydrochloride) is a potent new-generation ALK inhibitor with high activity against CNS metastases and a broad range of known crizotinib-resistant ALK mutations. It potently inhibits both wild-type ALK and ALK variants (C1156Y, F1174, G1202R, L1196M, S1206R, and T1151 mutants) with in vitro IC50s of. Category: Active pharmaceutical ingredients. CAS No. 2137030-98-7. Product ID: API2137030987. Molecular formula: C26H29Cl4FN6O3. Mole weight: 634.36. | |
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