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| Product | Description | |
|---|---|---|
| Endothelin 3, Human and Rat - CAS 117399-93-6 | Attenuates thrombin-evoked aggregation of human platelets. Group: Fluorescence/luminescence spectroscopy. |  |
| 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 3 human, rat | ?97% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| 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. Group: Biochemicals. Grades: Purified. CAS No. 112093-28-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| 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 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 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 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 Aldehyde | 99%, vial of 1 g, analytical standard. Group: Certified reference materials (crms). | |
| Endrin-ketone solution | 100 ng/?L in acetonitrile, analytical standard. Group: Pesticides & metabolites standards. | |
| 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 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 | Enfortumab is a monoclonal antibody targeting Nectin-4. Enfortumab has been used for the treatment of urothelial cancer. CAS No. 1448664-46-7. | |
| 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. | |
| 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 | 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 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. | |
| 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 salt | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Engasertib | Engasertib is an orally active highly specific AKT inhibitor with IC50 values of 0.13 μM, 0.09 μM and 2.75 μM for AKT1, AKT2 and AKT3, respectively. Engasertib inhibits AKT phosphorylation and modulates downstream signalling in vitro. Engasertib can inhibit cancer cell proliferation and tumor growth[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALM301. CAS No. 1313439-71-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-151504. | |
| 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. | |
| Englerin A | Englerin A is a potent and selective activator of TRPC4 and TRPC5 channels, with EC50s of 11.2 and 7.6 nM, respectively. Englerin A can induce renal carcinoma cells death by elevated Ca2+ influx and Ca2+ cell overload[1][2][3]. Uses: Scientific research. Group: Natural products. CAS No. 1094250-15-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-133168. | |
| 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. | |
| Enhanced Green Fluorescent Protein (EGFP) (200-208) | Enhanced Green Fluorescent Protein (EGFP) (200-208) is a marker gene product derived from the jellyfish Aequorea Victoria. Enhanced Green Fluorescent Protein (EGFP) (200-208) is a common reporter protein and is easy to detect[1]. Uses: Scientific research. Group: Peptides. CAS No. 323198-39-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2528. | |
| 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 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. | |
| 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. | |
| 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 |
| 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 | 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. | |
| 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. | |
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