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| Product | Description | |
|---|---|---|
| Endoproteinase GluC from Staphylococcus aureus, Recombinant | Protease S. aureus V8 (Endoproteinase-Glu-C) specifically cleaves peptide bonds on the COOH-terminal side of either aspartic or glutamic acids. In the presence of ammonium, the enzyme specificity is limited to glutamic sites. It has a molecular weight of 27 kDa daltons and optimum pH's of 4.0 and 7.8 with hemoglobin as the substrate. Protease S. aureus V8 is inhibited by diisopropylfluorophosphate and monovalent anions such as F-, Cl-, CH3COO-and NO3. Enzyme activity is determined by the casein digestion assay described by Drapeau. Endoproteinase gluc (staphylococcus aureus protease v8) is a serine proteinase which selectively cleaves peptide bonds c-terminal to...tide identification. Group: Enzymes. Synonyms: EC 3.4.21.19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. CAS No. 66676-43-5. V8 Protease. Mole weight: 29849 daltons. Activity: 38.3 μmol/min/mg. Storage: at -20°C. Form: Supplied freeze-dried from a Tris-HCl and sodium chloride buffer. Source: Bacillus subtilis. Species: Staphylococcus aureus. EC 3.4.21.19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. Cat No: NATE-1270. |  |
| Endoproteinase Lys-C | Endoproteinase Lys-C is a protease that cleaves proteins on the C-terminal side of lysine residues and is commonly used for protein sequencing [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 72561-05-8. Pack Sizes: 50 mg; 100 mg; 250 mg; 1 mg; 5 mg; 10 mg. Product ID: HY-P3208. |  |
| Endo S2, Streptococcus pyogenes | Endo-β-N-acetylglucosaminidase (Endo S2) is a key enzyme involved in the processing of free oligosaccharides in the cytosol. Endo-β-N-acetylglucosaminidase catalyzes hydrolysis of N-linked oligosaccharides [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 37278-88-9. Pack Sizes: 2 KU. Product ID: HY-E70069. | |
| Endosidin 2 | Endosidin 2 (ES2) is a cell-permeable benzylidene-benzohydrazide that binds to EXO70 subunit of the exocyst complex which results in inhibition of exocytosis and endosomal recycling in both plant and human cells and enhancement of plant vacuolar trafficking. Synonyms: ES2; 3-fluoro-benzoic acid, (2E)-2-[(4-hydroxy-3-iodo-5-methoxyphenyl)methylene]hydrazide; (E)-3-Fluoro-N'-(4-hydroxy-3-iodo-5-methoxybenzylidene)benzohydrazide. Grades: ≥98%. CAS No. 1839524-44-5. Molecular formula: C15H12FIN2O3. Mole weight: 414.2. |  |
| Endosulfan-II-D4 | Endosulfan-II-D4. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BETA-ENDOSULFAN D4;ENDOSULFAN-II-D4;endosulfan (beta isomer)d4. Product Category: Heterocyclic Organic Compound. CAS No. 203716-99-8. Molecular formula: C9H2Cl6D4O3S. Mole weight: 410.95. Purity: 97 atom % D. Product ID: ACM203716998. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Endosulfan Sulfate | Endosulfan Sulfate. Group: Biochemicals. Alternative Names: 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,3-Dioxide; 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dimethanol Cyclic Sulfate; 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dimethanol Cyclic Sulfate; 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,3-dioxide; 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,6-dioxide; Benzoepin Sulfate; Endosulfan III; Endosulfan Cyclic Sulfate; Endosulfan Sulfate; Endosulfate; Thiodan Sulfate. Grades: Highly Purified. CAS No. 1031-07-8. Pack Sizes: 100mg. Molecular Formula: C9H6Cl6O4S, Molecular Weight: 422.92. US Biological Life Sciences. |  Worldwide |
| Endosulfan Sulfate-d4 | Endosulfan Sulfate-d4. Group: Biochemicals. Alternative Names: 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,3-Dioxide-d4; 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dimethanol Cyclic Sulfate-d4; 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dimethanol Cyclic Sulfate-d4; 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,3-dioxide-d4; 6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3,6-dioxide-d4; Benzoepin Sulfate-d4; Endosulfan III-d4; Endosulfan Cyclic Sulfate-d4; Endosulfan Sulfate-d4; Endosulfate-d4; Thiodan Sulfate-d4. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C9H2D4Cl6O4S, Molecular Weight: 426.95. US Biological Life Sciences. | Worldwide |
| Endothall | Endothall (Endothal) is a protein phosphatase 2A ( PP2A ) inhibitor with IC 50 s of 90 nM and 5 μM for PP2A and PP1, respectively. Endothall can be used as an herbicide. Endothall also is useful in cancer chemotherapy [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Endothal. CAS No. 145-73-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-113976A. | |
| Endothall thioanhydride | Endothall thioanhydride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3a-alpha,4-beta,7-beta,7a-alpha)-hexahydro-4,7-epoxybenzo(c)thiophene-1,3-d;4,7-epoxybenzo(c)thiophene-1,3-dione,hexahydro-,(3a-alpha,4-beta,7-beta,7a-al;ENDOTHALL THIOANHYDRIDE. Product Category: Heterocyclic Organic Compound. CAS No. 109282-38-4. Molecular formula: C8H8O3S. Mole weight: 184.21. Product ID: ACM109282384. Alfa Chemistry ISO 9001:2015 Certified. | |
| Endothelial Progenitor Cells, Human Adult Normal, Cryopreserved, CD133+ (hEPC) | The endothelial progenitor cell (EPC) is a primitive cell type in the endothelial lineage. They are bone marrow originated cells with properties similar to those of embryonic angioblasts. These progenitor cells migrate into the blood stream and are capable of differentiating into a variety of mature vascular endothelial cell types. Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 500K Cells. US Biological Life Sciences. | Worldwide |
| Endothelial Progenitor Outgrowth Cells, Human Adult Normal, Cryopreserved (EPOC) | The endothelial progenitor cell (EPC) is a primitive cell type in the endothelial lineage. They are bone marrow originated cells with properties similar to those of embryonic angioblasts. These progenitor cells migrate into the blood stream and are capable of differentiating into a variety of mature vascular endothelial cell types. EPC play an important role in both angiogenesis and vasculogenesis. Recent evidence suggests the involvement of EPC in tumor growth and metastasis. Change in EPC number has been associated with lymphoma, multiple myeloma, Lewis lung tumor, and hepatocellular carcinoma (HCC). Alteration in EPC number and function has also been observed in pathogenesis of a variety of diseases including coronary artery disease (CAD), ischemia, pulmonary hypertension, cerebral vascular disease, acute myocardial infarction, diabetes mellitus, arthritis, and wound healing. In addition, EPC have impact on aging and smoking-related diseases, suggesting potential uses of EPC in thes Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 500K Cells. US Biological Life Sciences. | Worldwide |
| Endothelial Progenitor Outgrowth Cells, Human Adult Normal, Proliferating EPOC in T25 (EPOC) | The endothelial progenitor cell (EPC) is a primitive cell type in the endothelial lineage. They are bone marrow originated cells with properties similar to those of embryonic angioblasts. These progenitor cells migrate into the blood stream and are capable of differentiating into a variety of mature vascular endothelial cell types. Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 1M Cells. US Biological Life Sciences. | Worldwide |
| Endothelial Progenitor Outgrowth Cells, Mouse Adult Normal, Cryopreserved (EPOC, mEPOC) | Endothelial Progenitor Outgrowth Cells, Mouse Adult Normal, Cryopreserved (EPOC, mEPOC). Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 500K Cells. US Biological Life Sciences. | Worldwide |
| Endothelin-1 (human, porcine) trifluoroacetate salt | Endothelin-1 is a peptide vasoconstrictor that in humans is encoded by the EDN1 gene and produced by vascular endothelial cells. It is an agonist of endothelin (ET) receptors ETA and ETB (IC50s = 0.15 and 0.12 nM, respectively). Synonyms: ET-1. Grades: ≥95%. Molecular formula: C109H159N25O32S5·xCF3COOH. Mole weight: 2491.91. | |
| Endothelin 1 (swine, human) | Endothelin 1 (swine, human) is a synthetic peptide with the sequence of human and swine Endothelin 1, which is a potent endogenous vasoconstrictor. Endothelin 1 acts through two types of receptors ET A and ET B [1]. Uses: Scientific research. Group: Peptides. CAS No. 117399-94-7. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-P0202. | |
| Endothelin 1 (swine, human) | Endothelin 1 (swine, human), a vasoconstrictor increased in plasma and explants of patients with uterine leiomyomas, is a synthetic peptide with the sequence of human and swine Endothelin 1 and acts through two types of receptors ETA and ETB. Synonyms: Endothelin 1 swine, human; Endothelin 1; L-cysteinyl-L-seryl-L-cysteinyl-L-seryl-L-seryl-L-leucyl-L-methionyl-L-alpha-aspartyl-L-lysyl-L-alpha-glutamyl-L-cysteinyl-L-valyl-L-tyrosyl-L-phenylalanyl-L-cysteinyl-L-histidyl-L-leucyl-L-alpha-aspartyl-L-isoleucyl-L-isoleucyl-L-tryptophan (1->15),(3->11)-bis(disulfide); H-Cys(1)-Ser-Cys(2)-Ser-Ser-Leu-Met-Asp-Lys-Glu-Cys(2)-Val-Tyr-Phe-Cys(1)-His-Leu-Asp-Ile-Ile-Trp-OH. Grades: 95%. CAS No. 117399-94-7. Molecular formula: C109H159N25O32S5. Mole weight: 2491.9. | |
| Endothelin 1 (swine, human) (TFA) | Endothelin 1 (swine, human) (TFA) is a synthetic peptide with the sequence of human and swine Endothelin 1, which is a potent endogenous vasoconstrictor. Endothelin 1 acts through two types of receptors ET A and ET B [1]. Uses: Scientific research. Group: Peptides. CAS No. 394693-38-0. Pack Sizes: 500 μg; 5 mg; 10 mg. Product ID: HY-P0202A. | |
| Endothelin-2, human | Endothelin 2 is a ligand for the endothelin (ET) receptors and a potent vasoconstrictor mainly found in the kidney and intestine. Uses: Vasoconstrictor. Synonyms: Endothelin-2 (human, canine); Human endothelin-2; ET-2 (human); H-Cys(1)-Ser-Cys(2)-Ser-Ser-Trp-Leu-Asp-Lys-Glu-Cys(2)-Val-Tyr-Phe-Cys(1)-His-Leu-Asp-Ile-Ile-Trp-OH; L-cysteinyl-L-seryl-L-cysteinyl-L-seryl-L-seryl-L-tryptophyl-L-leucyl-L-alpha-aspartyl-L-lysyl-L-alpha-glutamyl-L-cysteinyl-L-valyl-L-tyrosyl-L-phenylalanyl-L-cysteinyl-L-histidyl-L-leucyl-L-alpha-aspartyl-L-isoleucyl-L-isoleucyl-L-tryptophan (1->15),(3->11)-bis(disulfide). Grades: ≥95%. CAS No. 123562-20-9. Molecular formula: C115H160N26O32S4. Mole weight: 2546.92. | |
| Endothelin-2 (human) trifluoroacetate salt | Endothelin-2 is a secretory peptide vasoconstrictor and ligand for the endothelin (ET) receptors ETA and ETB (Kbs= 32.8 and 1.33 nM, respectively). It displays similar selectivity for ETA and ETB endothelin receptors. Synonyms: ET-2. Grades: ≥95%. Molecular formula: C115H160N26O32S4·xCF3COOH. Mole weight: 2546.92. | |
| Endothelin-3, human, mouse, rabbit, rat | Endothelin 3 is a ligand of the endothelin (ET) receptors and a potent vasoconstrictor. Endothelin 3 increases blood pressure in spontaneously hypertensive and normotensive rats, and promotes migration and adhesion of enteric neural crest cells (ENCCs) to the embryonic gut in mice via interaction with ETB. Uses: Vasoconstrictor. Synonyms: Endothelin 3 (Rat,Human); ET-3 (Rat,Human); H-Cys(1)-Thr-Cys(2)-Phe-Thr-Tyr-Lys-Asp-Lys-Glu-Cys(2)-Val-Tyr-Tyr-Cys(1)-His-Leu-Asp-Ile-Ile-Trp-OH; L-cysteinyl-L-threonyl-L-cysteinyl-L-phenylalanyl-L-threonyl-L-tyrosyl-L-lysyl-L-alpha-aspartyl-L-lysyl-L-alpha-glutamyl-L-cysteinyl-L-valyl-L-tyrosyl-L-tyrosyl-L-cysteinyl-L-histidyl-L-leucyl-L-alpha-aspartyl-L-isoleucyl-L-isoleucyl-L-tryptophan (1->15),(3->11)-bis(disulfide). Grades: ≥97% by HPLC. CAS No. 117399-93-6. Molecular formula: C121H168N26O33S4. Mole weight: 2643.04. | |
| Endothelin-3, human, mouse, rabbit, rat TFA | Endothelin-3 is a peptide vasoconstricter and a ligand of the endothelin (ET) receptors ETA and ETB (Kbs = 1.05 and 1.49, respectively). It binds to G-protein-linked transmembrane receptors, ET-RA and ET-RB. Synonyms: Endothelin 3 (Rat,Human) (TFA); ET-3 (Rat,Human) (TFA); H-Cys(1)-Thr-Cys(2)-Phe-Thr-Tyr-Lys-Asp-Lys-Glu-Cys(2)-Val-Tyr-Tyr-Cys(1)-His-Leu-Asp-Ile-Ile-Trp-OH.TFA; L-cysteinyl-L-threonyl-L-cysteinyl-L-phenylalanyl-L-threonyl-L-tyrosyl-L-lysyl-L-alpha-aspartyl-L-lysyl-L-alpha-glutamyl-L-cysteinyl-L-valyl-L-tyrosyl-L-tyrosyl-L-cysteinyl-L-histidyl-L-leucyl-L-alpha-aspartyl-L-isoleucyl-L-isoleucyl-L-tryptophan (1->15),(3->11)-bis(disulfide) trifluoroacetic acid; Endothelin-3 (human, rat) trifluoroacetate salt. Grades: ≥95%. Molecular formula: C121H168N26O33S4.C2HF3O2. Mole weight: 2757.07. | |
| endothelin-converting enzyme 1 | A phosphoramidon-sensitive metalloendopeptidase in peptidase family M13 (neprilysin family). An integral membrane protein predominantly of endothelial cells, which generates the potent vasoconstrictor endothelin 1 from its inactive precursor. Group: Enzymes. Synonyms: endothelin-converting enzyme; ECE-1. Enzyme Commission Number: EC 3.4.24.71. CAS No. 138238-81-0. 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-4355; endothelin-converting enzyme 1; EC 3.4.24.71; 138238-81-0; endothelin-converting enzyme; ECE-1. Cat No: EXWM-4355. | |
| endothiapepsin | From the ascomycete Endothia parasitica. In peptidase family A1 (pepsin A family). Group: Enzymes. Synonyms: Endothia aspartic proteinase; Endothia acid proteinase; Endothia parasitica acid proteinase; Endothia parasitica aspartic proteinase. Enzyme Commission Number: EC 3.4.23.22. CAS No. 37205-60-0. 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-4260; endothiapepsin; EC 3.4.23.22; 37205-60-0; Endothia aspartic proteinase; Endothia acid proteinase; Endothia parasitica acid proteinase; Endothia parasitica aspartic proteinase. Cat No: EXWM-4260. | |
| Endotoxin Free Gold Nanoparticles | Endotoxin Free Gold Nanoparticles. Uses: Conjugate development (see our gold nanoparticle conjugation kits), immunostaining, lateral flow assays, biological sensor development (e.g. lspr-based assays), electron microscopy, dark field microscopy, surface enhanced raman spectroscopy (sers), etc. Group: other s. >99% reactant free. |  |
| Endotoxin Free Gold Nanourchins | Cytodiagnostics gold nanourchins are unique spherical gold nanoparticles with spiky protrusions, which result in absorption of light in the far-red. They are made using a unique proprietary protocol resulting in pure, reactant-free particles with excellent size distribution. Group: other s. | |
| Endotoxin free Transglutaminase 2 from Human tissue, Recombinant | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with a phosphate group as acceptor. Applications: Transglutaminase 2 catalyzes acyl transfer reactions from glutamine residues in proteins or peptides to primary amines, e. g. the formation of ε-(γ-glutamyl) lysine bonds between proteins by transferring the acyl group of a peptide-bound glutamine residue to the primary amino group of a peptide-bound lysine residue. transglutaminase 2 may also be used for immunoprecipitation. this product is suitable for cell culture use. Group: Enzymes. Synonyms: transglutaminase; ...rand et al., Anal. Biochem. 44 (221-231). Appearance: Liquid. Storage: Store working aliquots at ≤ - 20°C. Avoid repeated freezing and thawing. Form: The transglutaminase is supplied in 10 mM Tris-HCl pH 7.2, 150 mM NaCl, 0.5 mM EDTA, 0.5 mM DTT, 10% Glycerol. Source: Insect cells. Species: Human. transglutaminase; EC 2.3.2.13; 80146-85-6; transglutaminase; Factor XIIIa; fibrinoligase; fibrin stabilizing factor; glutaminylpeptide γ-glutamyltransferase; polyamine transglutaminase; tissue transglutaminase; R-glutaminyl-peptide:amine γ-glutamyl transferase; protein-glutamine γ-glutamyltransferase; TG1. Pack: 250 μg; 1mg. Cat No: NATE-1729. | |
| Endotoxin inhibitor | Endotoxin inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LYS-THR-LYS-CYS-LYS-PHE-LEU-LYS-LYS-CYS;ENDOTOXIN INHIBITOR;H-LYS-THR-LYS-CYS-LYS-PHE-LEU-LYS-LYS-CYS-OH;K-T-K-C-K-F-L-K-K-C;H-Lys-Thr-Lys-Cys-Lys-Phe-Leu-Lys-Lys-Cys-OH (Disulfide bond). Product Category: Heterocyclic Organic Compound. CAS No. 147396-10-9. Molecular formula: C55H97N15O12S2. Mole weight: 1224.58. Product ID: ACM147396109. Alfa Chemistry ISO 9001:2015 Certified. | |
| Endotrophin (mouse) | Endotrophin, a carboxy-terminal cleavage product of the collagen 6α-3 chain produced and released by adipocytes, is greatly upregulated in malignant tumors of the breast, liver colon and pancreas. Endotrophin provides a link between obesity and aggressive tumor growth and may serve as a sensitive diagnostic marker and effective therapeutic target for designing better treatments for cancer and improving obesity-induced insulin resistance. Synonyms: H-Thr-Glu-Pro-Leu-Phe-Leu-Thr-Lys-Thr-Asp-Ile-Cys-Lys-Leu-Ser-Arg-Asp-Ala-Gly-Thr-Cys-Val-Asp-Phe-Lys-Leu-Leu-Trp-His-Tyr-Asp-Leu-Glu-Ser-Lys-Ser-Cys-Lys-Arg-Phe-Trp-Tyr-Gly-Gly-Cys-Gly-Gly-Asn-Glu-Asn-Arg-Phe-His-Ser-Gln-Glu-Glu-Cys-Glu-Lys-Met-Cys-Ser-Pro-Glu-Leu-Thr-Val-OH (Disulfide bridge: Cys12-Cys62, Cys21-Cys45, Cys37-Cys58, air oxidized). Grades: ≥95%. CAS No. 1678414-54-4. Molecular formula: C345H520N92O106S7. Mole weight: 7876.94. | |
| Endoxifen | Endoxifen is a key active metabolite of tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity. Endoxifen has the potential for breast cancer study [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 110025-28-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18719E. | |
| Endoxifen | Endoxifen. Group: Biochemicals. Grades: Purified. CAS No. 112093-28-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Endoxifen E-isomer hydrochloride | The hydrochloride salt form of E-isomer of Endoxifen which is a significant metamolite of Tamoxifen, could be a regulator of estrogen receptor and could be effective in the treatment of estrogen-dependent breast cancer. Uses: The hydrochloride salt form of e-isomer of endoxifen which could be a regulator of estrogen receptor and could be effective in the treatment of estrogen-dependent breast cancer. Synonyms: E-Endoxifen hydrochloride. Grades: 98%. CAS No. 1197194-61-8. Molecular formula: C25H28ClNO2. Mole weight: 409.95. | |
| Endoxifen E-isomer hydrochloride | Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride), an E-isomer of Endoxifen, is an impurity in Endoxifen Z-isomer agent substance. Endoxifen E-isomer hydrochloride exhibits antiestrogenic effects [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E-Endoxifen hydrochloride. CAS No. 1197194-61-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-18719C. | |
| Endoxifen HCl | Endoxifen HCl, the active metabolite of Tamoxifen, ia a potent and selective estrogen receptor antagonist. Phase 2. Endoxifen shows anti-estrogenic effects, and decreases the E2-induced PR expression in MCF-7 cells. In vivo, Endoxifen (8 mg/kg, ) inhibits growth of MCF-7 human mammary tumor xenografts in mice. Synonyms: Z-Endoxifen HCl; Z Endoxifen HCl; ZEndoxifen HCl; Z Endoxifen Hydrochloride; ZEndoxifen Hydrochloride. Grades: 98%. CAS No. 1032008-74-4. Molecular formula: C25H28ClNO2. Mole weight: 409.95. | |
| Endoxifen hydrochloride | Endoxifen hydrochloride is a key active metabolite of Tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity. Endoxifen hydrochloride has the potential for breast cancer study [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1197194-41-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18719B. | |
| Endoxifen hydrochloride | Endoxifen hydrochloride is a metabolite of Tamoxifen and a selective estrogen receptor modulator (SERM) that inhibits the growth of estrogen-stimulated BT474 cells (IC50 = 54 nM). Endoxifen is used for the treatment of estrogen receptor (ER) positive breast cancer. Uses: Anticancer drug. Synonyms: 4-[1-[4-[2-(methylamino)ethoxy]phenyl]-2-phenyl-1-buten-1-yl]-Phenol hydrochloride (1:1). Grades: 99%. CAS No. 1197194-41-4. Molecular formula: C25H28ClNO2. Mole weight: 409.95. | |
| Endrin Ketone | Endrin Ketone. Uses: For analytical and research use. Group: Impurity standards. CAS No. 53494-70-5. Molecular Formula: C12H9Cl5O. Mole Weight: 346.45. Catalog: APB53494705. |  |
| enduracididine β-hydroxylase | Fe2+-dependent enzyme. The enzyme is involved in biosynthesis of the nonproteinogenic amino acid β-hydroxyenduracididine, a component of the mannopeptimycins (cyclic glycopeptide antibiotic), produced by Streptomyces hygroscopicus NRRL 30439. Group: Enzymes. Synonyms: MppO; L-enduracididine,2-oxoglutarate:O2 oxidoreductase (3-hydroxylating). Enzyme Commission Number: EC 1.14.11.40. 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-0659; enduracididine β-hydroxylase; EC 1.14.11.40; MppO; L-enduracididine,2-oxoglutarate:O2 oxidoreductase (3-hydroxylating). Cat No: EXWM-0659. | |
| Enduracidin | It is produced by the strain of Streptomyces fungicidicus. Enramycin is a polypeptide antibiotic, and it has anti-gram-positive bacteria and mycobacterium activity. Enramycin is composed of two different compounds: Enramycin A and enramycin B. Synonyms: Enramycin; Enramycin Premix; Enramicina; Enramycinum; Enradin. Grades: >95%. CAS No. 11115-82-5. Molecular formula: C107H138Cl2N26O31 (Enramycin A); C108H140Cl2N26O31 (Enramycin B). Mole weight: 2550.21 (Enramycin A); 2564.24 (Enramycin B). | |
| Enduracidin A | It is produced by the strain of Streptomyces fungicidicus. It has anti-gram-positive bacteria and mycobacterium activity. Synonyms: 1-Oxa-4, 7, 10, 13, 16, 19, 22, 25, 28, 31, 34, 37, 40, 43, 46-pentadecaazacyclononatetracontane, enduracidin A derivative; [1(Z,E),10(R),15(R)]-N-(10-Methyl-1-oxo-2,4-undecadienyl)-L-α-aspartyl-L-threonyl-D-2-(4-hydroxyphenyl)glycyl-D-ornithyl-D-allothreonyl-L-2-(4-hydroxyphenyl)glycyl-D-2-(4-hydroxyphenyl)glycyl-L-allothreonyl-N5-(aminocarbonyl)-L-ornithyl-3-(2-amino-4,5-dihydro-1H-imidazol-4-yl)-D-alanyl-L-2-(4-hydroxyphenyl)glycyl-D-seryl-L-2-(3,5-dichloro-4-hydroxyphenyl)glycylglycyl-3-(2-amino-4,5-dihydro-1H-imidazol-4-yl)-L-alanyl-D-alanyl-L-2-(4-hydroxyphenyl)glycine 1-lactone; Enramycin A. Grades: >95%. CAS No. 34438-27-2. Molecular formula: C107H138Cl2N26O31. Mole weight: 2355.30. | |
| Enduracidin A hydrochloride | It is produced by the strain of Streptomyces fungicidicus. It has anti-gram-positive bacteria and mycobacterium activity. Synonyms: Enduracidin A HCl; Enramycin A hydrochloride. CAS No. 33368-20-6. Molecular formula: C107H138Cl2N26O31.HCl. Mole weight: 2391.76. | |
| Enduracidin B | It is produced by the strain of Streptomyces fungicidicus. It has anti-gram-positive bacteria and mycobacterium activity. Synonyms: Enramycin B. Grades: >95%. CAS No. 34304-21-7. Molecular formula: C108H140Cl2N26O31. Mole weight: 2369.32. | |
| Enduracidin B hydrochloride | It is produced by the strain of Streptomyces fungicidicus. It has anti-gram-positive bacteria and mycobacterium activity. Synonyms: Enduracidin B HCl; Enramycin B hydrochloride. CAS No. 34765-98-5. Molecular formula: C108H140Cl2N26O31.HCl. Mole weight: 2405.78. | |
| Enduracidin hydrochloride (Enramycin) | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C107H138Cl2N26O31. CAS No. 11115-82-5. Prepack ID 53593712-1g. Molecular Weight 2355.3. See USA prepack pricing. |  |
| Endusamycin | Endusamycin is produced by the strain of Streptomyces endus subsp. aureus. It has activity against gram-positive bacteria, some anaerobic bacteria, Eimeria tenella, E.acervulina. The feed with mycorycin of 10-40 μg/g was effective for coccidioides infection. Synonyms: Dianemycin, 19-de((tetrahydro-5-methoxy-6-methyl-2H-pyran-2-yl)oxy)-15-((tetrahydro-5-methoxy-6-methyl-2H-pyran-2-yl)oxy)-, (15(2S,5S,6R))-. CAS No. 100242-41-9. Molecular formula: C47H78O14. Mole weight: 867.11. | |
| Enecadin | Enecadin is a neuroprotective agent extracted from patent US 8623823 B2. Uses: Scientific research. Group: Signaling pathways. CAS No. 259525-01-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100119. | |
| Ene Reductases | asymmetric double bond reduction. Group: Enzymes. Synonyms: Ene Reductases; ERED. Form: 1. Enzyme Powder: 29 items*50mg / item, or other quantity2. Screening Kit: 29 items*1mg / item. Ene Reductases; ERED; Screening Kit; library of enzyme; enzyme library. Cat No: ENLC-006. | |
| Enflicoxib | Enflicoxib (E 6087) is a nonsteroidal anti-inflammatory compound that selectively inhibits cyclooxygenase-2 ( COX-2 ). Enflicoxib does not inhibit cyclooxygenase-1 (COX-1). E-6087 shows anti-inflammatory, analgesic and antipyretic activities in animal models [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: E 6087. CAS No. 251442-94-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19384. | |
| Enflurane | Enflurane, a volatile anaesthetic, is a potent inhibitor of high conductance Ca 2+ -activated K+ channels of Chara australis. Enflurane is an internal standard in monitoring halogenated volatile anaesthetics by headspace gas chromatography-mass spectrometry [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 13838-16-9. Pack Sizes: 100 mg. Product ID: HY-A0135. | |
| Enflurane | Enflurane. Group: Biochemicals. Alternative Names: 2-Chloro-1,1,2-trifluoroethyl difluoromethyl ether; 4-Chloro-1H,4H-perfluoro(2-oxabutane). Grades: Highly Purified. CAS No. 13838-16-9. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C3H2ClF5O. US Biological Life Sciences. | Worldwide |
| Enfortumab | Enfortumab is a monoclonal antibody targeting Nectin-4. Enfortumab has been used for the treatment of urothelial cancer. CAS No. 1448664-46-7. | |
| Enfortumab | Enfortumab is a humanized derived anti- Nectin-4 antibody that can be conjugated with the highly efficient microtubule disruptor MMAE (HY-15162) to generate the antibody drug conjugate (ADC) Enfortumab vedotin (HY-P99016A). Enfortumab can be used for the study of locally advanced and metastatic urothelial carcinoma [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1448664-46-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99016. | |
| Enfortumab vedotin-ejfv | Enfortumab vedotin-ejfv is an anti- Nectin-4 antibody-drug conjugate. Enfortumab vedotin-ejfv is a fully humanized IgG1 antibody conjugated to the microtubule disrupting agent MMAE (HY-15162) via a protease-cleavable maleimidocaproylvaline-citrulline linker (SGD-1006). Nectin-4 is an adhesion protein involved in cellular processes and tumorigenesis, and Enfortumab vedotin-ejfv is indicated for the inhibition of locally advanced or metastatic urothelial carcinoma [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1346452-25-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99016A. | |
| Enfortumab vedotin-ejfv (solution) | Enfortumab vedotin-ejfv (solution) is an anti- Nectin-4 antibody-drug conjugate. Enfortumab vedotin-ejfv is a fully humanized IgG1 antibody conjugated to the microtubule disrupting agent MMAE (HY-15162) via a protease-cleavable maleimidocaproylvaline-citrulline linker (SGD-1006). Nectin-4 is an adhesion protein involved in cellular processes and tumorigenesis, and Enfortumab vedotin-ejfv is indicated for the inhibition of locally advanced or metastatic urothelial carcinoma [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1346452-25-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99016B. | |
| Enfumafungin | Enfumafungin is a triterpene glycoside and hemiacetal isolated from a fermentation of Hormonema sp. Enfumafungin is an antifungal agent that acts on fungal cell walls as an inhibitor of (1,3)-beta-D-glucan synthase. It is specific for yeast and fungi (excluding Cryptococcus) and does not inhibit the growth of Bacillus subtilis. Synonyms: 4H-1,4a-Propano-2H-phenanthro[1,2-c]pyran-7-carboxylic acid, 14-(acetyloxy)-8-[(1R)-1,2-dimethylpropyl]-15-(β-D-glucopyranosyloxy)-1,6,6a,7,8,9,10,10a,10b,11,12,12a-dodecahydro-4-hydroxy-1,6a,8,10a-tetramethyl-, (1S, 4aR, 6aS, 7R, 8R, 10aR, 10bR, 12aS, 14R, 15R)-. Grades: ≥98%. CAS No. 260979-95-1. Molecular formula: C38H60O12. Mole weight: 708.88. | |
| Enfumafungin | Enfumafungin. Uses: For analytical and research use. Group: Impurity standards. CAS No. 260979-95-1. Molecular Formula: C38H60O12. Mole Weight: 708.89. Catalog: APB260979951. | |
| Enfuvirtide | Enfuvirtide (T20;DP178) is an anti- HIV-1 fusion inhibitor peptide. Uses: Scientific research. Group: Peptides. Alternative Names: T20; DP178. CAS No. 159519-65-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0052. | |
| Enfuvirtide | Enfuvirtide is a biomimetic peptide of HIV-1 fusion inhibitor with CD4+ cells and it is used to patients with multi-drug resistant HIV. Enfuvirtide binds to gp41 preventing the creation of an entry pore for the HIV-1 virus. Synonyms: N-Acetyl-L-tyrosyl-L-threonyl-L-seryl-L-leucyl-L-isoleucyl-L-histidyl-L-seryl-L-leucyl-L-isoleucyl-L-α-glutamyl-L-α-glutamyl-L-seryl-L-glutaminyl-L-asparaginyl-L-glutaminyl-L-glutaminyl-L-α-glutamyl-L-lysyl-L-asparaginyl-L-α-glutamyl-L-glutaminyl-L-α-glutamyl-L-leucyl-L-leucyl-L-α-glutamyl-L-leucyl-L-α-aspartyl-L-lysyl-L-tryptophyl-L-alanyl-L-seryl-L-leucyl-L-tryptophyl-L-asparaginyl-L-tryptophyl-L-phenylalaninamide; DP 178; ENF; Fuzeon; GP 41-127-162AA; Pentafuside; T 20; T 20 (peptide); Ac-Tyr-Thr-Ser-Leu-Ile-His-Ser-Leu-Ile-Glu-Glu-Ser-Gln-Asn-Gln-Gln-Glu-Lys-Asn-Glu-Gln-Glu-Leu-Leu-Glu-Leu-Asp-Lys-Trp-Ala-Ser-Leu-Trp-Asn-Trp-Phe-NH2. Grades: ≥98%. CAS No. 159519-65-0. Molecular formula: C204H301N51O64. Mole weight: 4491.88. | |
| Enfuvirtide | Enfuvirtide (T20;DP178) is an anti-HIV-1 fusion inhibitor peptide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Enfuvirtide; T-2;Enfuvirtide Acetate (T-20);ENFUVIRTIDE(T-20) 98+%;Enfurvitide(T-20);Pentafuside;Ac-Tyr-Thr-Ser-Leu-Ile-His-Ser-Leu-Ile-Glu-Glu-Ser-Gln-Asn-Gln-Gln-Glu-Lys-Asn-Glu-Gln-Glu-Leu-Leu-Glu-Leu-Asp-Lys-Trp-Ala-Ser-Leu-Trp-Asn-Trp-Phe-NH{2};Enf. Product Category: Inhibitors. CAS No. 159519-65-0. Molecular formula: C204H301N51O64. Mole weight: 4491.9. Purity: >95%. Density: 1.59g/cm³. Product ID: ACM159519650. Alfa Chemistry ISO 9001:2015 Certified. | |
| Enfuvirtide acetate | Enfuvirtide (T20; DP178) acetate is an anti-HIV-1 fusion inhibitor peptide. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 914454-00-5. Molecular formula: C206H305N51O66. Mole weight: 4552.62. Purity: 0.96. IUPACName: 2-(3,5-dimethylpyrazol-1-yl)-3-(4-methylpiperazin-1-yl)quinoxaline. Canonical SMILES: CC1=CC(=NN1C2=NC3=CC=CC=C3N=C2N4CCN(CC4)C)C. Product ID: ACM914454005. Alfa Chemistry ISO 9001:2015 Certified. | |
| Enfuvirtide acetate | Enfuvirtide (T20; DP178) acetate is an anti- HIV-1 fusion inhibitor peptide. Uses: Scientific research. Group: Peptides. Alternative Names: T20 acetate; DP178 acetate. CAS No. 914454-00-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0052A. | |
| Engeletin | Engeletin. Group: Biochemicals. Grades: Highly Purified. CAS No. 572-31-6. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. US Biological Life Sciences. | Worldwide |
| Engineering Plastic | Engineering Plastic. Group: Polymers. | |
| Engineering plastics | Engineering plastics. Group: Polymers. | |
| Englitazone sodium | Englitazone sodium is a novel blocker of NSCa and KATP channels. It is an antidiabetic agent. Uses: Englitazone sodium is an antidiabetic agent. Synonyms: CP-72467-2;CP72467-2;(-)-5-(((2R)-2-Benzyl-6-chromanyl)methyl)-2,4-thiazolidinedione, sodium salt;Sodium;5-[[(2R)-2-benzyl-3,4-dihydro-2H-chromen-6-yl]methyl]-1,3-thiazolidin-3-ide-2,4-dione;2,4-Thiazolidinedione,5-[[3,4-dihydro-2-(phenylmethyl)-2H-1-benzopyran-6-yl]methyl]-, sodium salt. Grades: >98%. CAS No. 109229-57-4. Molecular formula: C20H18NNaO3S. Mole weight: 375.42. | |
| Enhancer of rudimentary homolog | ERH is a small, highly conserved protein that has been found in Sus scrofa. It has antibacterial activity. Synonyms: ERH. | |
| Enibarcimab | Enibarcimab is a humanised murine monoclonal immunoglobulin G1 ( IgG1 ) antibody, could be used for acute heart failure, COVID-19 infections and septic shock research [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2305638-98-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99177. | |
| Enibarcimab | Enibarcimab is a humanized monoclonal antibody that has been investigated as a medication for the treatment of acute heart failure and COVID-19. Synonyms: HAM 8101; HAM-8101; HAM8101. CAS No. 2305638-98-4. | |
| Eniluracil | Eniluracil, also known as GW776 and GW776C85, is an orally active and irreversible inhibitor of dihydropyrimidine dehydrogenase. Eniluracil inhibits dihydropyrimidine dehydrogenase, the rate-limiting enzyme that catabolizes and inactivates 5-fluorouracil (5-FU) in the liver. Co-administration of ethynyluracil permits the oral administration of 5-FU. Uses: Enzyme inhibitors. Synonyms: 5-ethynyluracil; 5-ethynylpyrimidine-2,4(1H,3H)-dione; 5-Ethynyl-2-hydroxypyrimidin-4(1H)-one; GW776; GW-776; GW 776. CAS No. 59989-18-3. Molecular formula: C6H4N2O2. Mole weight: 136.11. | |
| Eniluracil | Eniluracil (5-Ethynyluracil) is an orally active dihydropyrimidine dehydrogenase ( DPD ) inhibitor. Eniluracil irreversibly inhibits DPD , increases the oral bioavailability of 5-fluorouracil to 100%, and facilitates the uniform absorption and toxicity of 5-fluorouracil. Eniluracil can be used in cancer research of combination with fluoropyrimidines (including 5-fluorouracil) [1] [2]. Eniluracil is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Ethynyluracil; GW776C85. CAS No. 59989-18-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10533. | |
| Eniluracil | Potent inactivator of Dihydropyrimidine dehydrogenase (DPD). Group: Biochemicals. Alternative Names: 5-Ethynyl-2,4(1H,3H)-pyrimidinedione; 5-Ethynyluracil; NSC 687296. Grades: Highly Purified. CAS No. 59989-18-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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