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| Product | Description | |
|---|---|---|
| EGCG Octaacetate | EGCG Octaacetate (AcEGCG) is a proagent of Green tea epigallocatechin-3-gallate (EGCG). EGCG Octaacetate decreases the proinflammatory mediator levels by down-regulating of PI3K/Akt/NFκB phosphorylation and p65 acetylation. EGCG octaacetate is the potential antibacterial compound for gram-positive bacteria (GPB) and gram-negative bacteria (GNB). EGCG Octaacetate exhibits antioxidant, anti-angiogenesis, anti-inflammatory and antitumor activities[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AcEGCG; Peracetylated (-)-epigallocatechin-3-gallate. CAS No. 148707-39-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N6263. |  |
| EGDS | EGDS. Alternative Names: EGDS; Ethylene glycol distearate. Grades: 190.0~210.0(KOHmg/g). CAS No. 627-83-8. Molecular formula: C38H74O4. Mole weight: 594.99. |  |
| Ege I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (HindIII-digest) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 5-fold overdigestion with enzyme 70% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 200U; 1000U. GGC↑GCC CCG↓CGG. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer B, BSA. Storage: -20°C. Form: Liquid. Source: Enterobacter gergoviae. Pack: 10 mM Tris-HCl (pH 7.5); 250 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 50% glycerol. Cat No: ET-1103RE. |  |
| EGF816 | EGF816, also called as Nazartinib, a covalent mutant-selective EGFR inhibitor and potently inhibits the T790M resistance mutation while sparing wild-type EGFR. in vivo: demonstrated strong tumor regressions in several EGFR activating and resistant tumor m. Alternative Names: EGF816; EGF-816; EGF 816; NVS-816; NVS 816; NVS816; Nazartinib; N-[7-chloro-1-[(3R)-1-[(E)-4-(dimethylamino)but-2-enoyl]azepan-3-yl]benzimidazol-2-yl]-2-methylpyridine-4-carboxamideEGF816UNII-KE7K32EME8KE7K32EME8EGF-8161508250-71-2GTPL9204SCHEMBL16767232SCHEMBL16767240EGF 816compound 47 [PMID: 27433829]. CAS No. 1508250-71-2. Molecular formula: C26H31ClN6O2. Mole weight: 495.02. | |
| EGF-A Peptide | EGF-A Peptide. Alternative Names: Gly-Thr-Asn-Glu-Cys-Leu-Asp-Asn-Asn-Gly-Gly-Cys-Ser-His-Val-Cys-Asn-Asp-Leu-Lys-Ile-Gly-Tyr-Glu-Cys-Leu-Cys-Pro-Asp-Gly-Phe-Gln-Leu-Val-Ala-Gln-Arg-Arg-Cys-Glu-Asp-Ile-NH2 (Disulfide bond Cys5/Cys16, Cys12/Cys25, Cys27/Cys39). Molecular formula: C188H292N58O65S6. Mole weight: 4597.00. | |
| EGFP saRNA (5mCTP) | EGFP saRNA (5mCTP) is a self-amplifying RNA designed to express Enhanced Green Fluorescent Protein (EGFP), which emits bright green fluorescence with an excitation maximum at 488 nm and an emission maximum at 509 nm. This saRNA is modified with 5-methylcytidine triphosphate (5mCTP) to enhance stability and suppress RNA-mediated innate immune activation. It features a Cap1 structure and includes a poly(A) tail to further improve expression efficiency. EGFP saRNA is ideal for analyzing mRNA delivery and translation efficiency, as well as for optimizing delivery formulations in various applications. Uses: Reporter gene sarna. Alternative Names: EGFP saRNA (5-methylcytidine triphosphate). | |
| EGF-R (1138-1147) | A peptide fragment of EGF-R. Epidermal growth factor receptor (EGFR) is a prototypic cell-surface receptor belonging to the ErbB/HER onocogene family. Targeting of EGFR with specific blocking antibodies or inhibitors have been developing for treatment for EGFR-associated tumors. Alternative Names: Epidermal growth factor receptor (1138-1147). | |
| EGF Receptor (985-996) (human) | EGF Receptor (985-996) (human) exists on the cell surface and is activated by the binding of its specific ligands. EGFR belongs to the tyrosine kinase receptor (RTK) ErbB family. Alternative Names: L-Glutamine, L-α-aspartyl-L-valyl-L-valyl-L-α-aspartyl-L-alanyl-L-α-aspartyl-L-α-glutamyl-L-tyrosyl-L-leucyl-L-isoleucyl-L-prolyl-; L-Glutamine, N2-[1-[N-[N-[N-[N-[N-[N-[N-[N-(N-L-α-aspartyl-L-valyl)-L-valyl]-L-α-aspartyl]-L-alanyl]-L-α-aspartyl]-L-α-glutamyl]-L-tyrosyl]-L-leucyl]-L-isoleucyl]-L-prolyl]-; L-α-Aspartyl-L-valyl-L-valyl-L-α-aspartyl-L-alanyl-L-α-aspartyl-L-α-glutamyl-L-tyrosyl-L-leucyl-L-isoleucyl-L-prolyl-L-glutamine; H-Asp-Val-Val-Asp-Ala-Asp-Glu-Tyr-Leu-Ile-Pro-Gln-OH; Epidermal Growth Factor Receptor Peptide. Grades: ≥95%. CAS No. 96249-43-3. Molecular formula: C61H93N13O23. Mole weight: 1376.46. | |
| EGF Receptor Antibody [K22M8] | EGF Receptor,EGFR,Epidermal Growth Factor Receptor. Group: Antibodies. Alternative Names: EGF Receptor,EGFR,Epidermal Growth Factor Receptor. Pack Sizes: 20ul. Product ID: F0053. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. |  United States; Europe |
| EGF Receptor Substrate 2 Phospho-Tyr5 | EGF Receptor Substrate 2 Phospho-Tyr5 is a bioactive peptide derived from the autophosphorylation site (Tyr992) of the epidermal growth factor receptor (EGFR). Alternative Names: H-Asp-Ala-Asp-Glu-pTyr-Leu-Ile-Pro-Gln-Gln-Gly-OH. Grades: ≥95%. Molecular formula: C54H82N13O24. Mole weight: 1328.28. | |
| EGFR-IN-12 | EGFR-IN-12 is a 4,6-disubstituted pyrimidine and is a potent, ATP-competitive, irreversible and highly selective EGFR inhibitor with an IC50of 21 nM. EGFR-IN-12 also inhibits mutant EGFRL858R and EGFRL861Q with IC50s of 63 nM and 4 nM, respectively. EGFR-IN-12 displays strong selectivity for EGFR over HER4 (IC50 = 7640 nM) and a panel of 55 other kinases. EGFR-IN-12 induces cells apoptosis and has antitumor activity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 879127-07-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17499. | |
| EGFR-IN-5 | EGFR-IN-5 is a EGFR inhibitor with IC50s of 10.4, 1.1, 34, 7.2 nM for EGFR, EGFRL858R, EGFRL858R/T790M, and EGFRL858R/T790M/C797S, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 2225887-26-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111415. | |
| EGFR-IN-7 | EGFR-IN-7 Inhibitor. Uses: Scientific use. Product Category: T11161. CAS No. 2267329-76-8. |  |
| EGFR-IN-7 | EGFR-IN-7 is a potent, selective and orally active EGFR kinase inhibitor. EGFR-IN-7 has inhibitory effect for for EGFR (WT) and EGFR (mutant C797S/T790M/L858R) with IC50 values of 7.92 nM and 0.218 nM, respectively. EGFR-IN-7 can be used for the research of various cancers[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2267329-76-8. Pack Sizes: 5 mg; 10 mg; 50 mg. Product ID: HY-128862. | |
| EGFR-IN-70 | EGFR-IN-70 (compound 18j) is a potent EGFR inhibitor with IC50 values of 23.6 and 307.5 nM for EGFRLR/TM/CS and EGFRWT, respectively. EGFR-IN-70 has anti-proliferative activity and suppresses phosphorylation of the EGFR. EGFR-IN-70 can be used for cancer research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2926716-96-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150611. | |
| EGFR-IN-86 | EGFR-IN-86 (compound 4i) is an EGFR inhibitor (IC50: 1.5 nM) with high activity against glioblastoma. EGFR-IN-86 induces apoptosis and arrests the U87 cell cycle in the G2/M phase[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3055550-22-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-149530. | |
| EGFR-IN-95 | EGFR-IN-95 (compound 5j) is an 2,4-diaminonicotinamide derivative. EGFR-IN-95 has potent inhibitory activity against EGFR del19/T790M/C797S and L858R/T790M/C797S[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3027135-04-9. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-163094. | |
| EGFR-IN-99 | EGFR-IN-99 (compound 1a) is a potent EGFR and HER2 Exon 20 insertion mutant inhibitor. EGFR-IN-99 has excellent antiproliferative activity against DFCI127 cells, with an EC50 of 11.5 nM. EGFR-IN-99 can be used for the research of non-small cell lung cancer (NSCLC)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2068806-31-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-123766. | |
| EGFR kinase inhibitor 3 | EGFR kinase inhibitor 3 (compound 2) is a bivalent ATP-allosteric EGFR kinase inhibitor with IC50s of <10 nM, 1.5 nM, 0.059 nM, 0.064 nM for WT EGFR, EGFR-activating mutations L858R, L858R/T790M and L858R/T790M/C797S, respectively. EGFR kinase inhibitor 3 is a C-linked inhibitor[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2922402-03-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-162299. | |
| EGFRvIII peptide (PEPvIII) | EGFRvIII peptide (PEPvIII), a tumor-specific mutation and a target for anti-tumor immunotherapy, is widely expressed in glioblastoma multiforme (GBM) and other tumors, and its expression enhances tumorigenicity. Alternative Names: H-Leu-Glu-Glu-Lys-Lys-Gly-Asn-Tyr-Val-Val-Thr-Asp-His-Cys-OH; L-leucyl-L-alpha-glutamyl-L-alpha-glutamyl-L-lysyl-L-lysyl-glycyl-L-asparagyl-L-tyrosyl-L-valyl-L-valyl-L-threonyl-L-alpha-aspartyl-L-histidyl-L-cysteine. Grades: ≥95%. CAS No. 129112-17-0. Molecular formula: C70H111N19O24S. Mole weight: 1634.81. | |
| Eggcrate Charcoal Firm Foam | With its classic shape, our high-quality eggcrate charcoal firm foam offers extra cushioning and airflow while still being one of the most economical choices on the market today. It replicates the effects of standard charcoal firm sheet foam more economically, due to our cutting process and the shape adds extra benefits. |  |
| Eggcrate Charcoal Regular Foam | With its familiar, classic design, charcoal regular eggcrate foam replicates the effects of charcoal regular sheet foam more economically, due to our cutting process. Its non-soiling surface makes it appropriate for use in any area charcoal regular foam can be applied. | |
| Eggcrate-Charcoal Regular Foam Top/Lid | Eggcrate toppers and lids are a perfect complement to your custom packaging or casing when placed over your Pick and Pull Grid core design. | |
| Eggcrate Pink Anti-Static Foam Top/Lid | Eggcrate toppers and lids are a perfect complement to your custom packaging or casing when placed over your Pick and Pull Grid core design. | |
| Egg Laying Hormone, aplysia | Egg Laying Hormone, aplysia is a neuropeptide containing 36 amino acids synthesized by the neurons of the bag cell, which can stimulate oviposition and ovulation in Aplysia by electrical discharge triggering of neurons. Egg Laying Hormone, aplysia induces a voltage-dependent slow inward current carried by Na+ in an identified motoneuron. Alternative Names: Egg-laying hormone (Aplysia brasiliana bag cell); Ile-Ser-Ile-Asn-Gln-Asp-Leu-Lys-Ala-Ile-Thr-Asp-Met-Leu-Leu-Thr-Glu-Gln-Ile-Arg-Glu-Arg-Gln-Arg-Tyr-Leu-Ala-Asp-Leu-Arg-Gln-Arg-Leu-Leu-Glu-Lys-NH2; ELH, aplysia; L-Lysinamide, L-isoleucyl-L-seryl-L-isoleucyl-L-asparaginyl-L-glutaminyl-L-a-aspartyl-L-leucyl-L-lysyl-L-alanyl-L-isoleucyl-L-threonyl-L-a-aspartyl-L-methionyl-L-leucyl-L-leucyl-L-threonyl-L-a-glutamyl-L-glutaminyl-L-isoleucyl-L-arginyl-L-a-glutamyl-L-arginyl-L-glutaminyl-L-arginyl-L-tyrosyl-L-leucyl-L-alanyl-L-a-aspartyl-L-leucyl-L-arginyl-L-glutaminyl-L-arginyl-L-leucyl-L-leucyl-L-a-glutamyl-. Grades: ≥95%. CAS No. 117680-39-4. Molecular formula: C190H329N59O57S. Mole weight: 4384.20. | |
| Egg Liss Rhod PE | Egg Liss Rhod PE is a fluorescent labelling lipid. Alternative Names: L-α-Phosphatidylethanolamine-N-(lissamine rhodamine B sulfonyl) (Ammonium Salt) (Egg-Transphosphatidylated, Chicken). Grades: >99%. CAS No. 383906-59-0. Molecular formula: C66H107N4O14PS2. Mole weight: 1275.67. | |
| Egg oil | Egg oil is a natural oil, which consists primarily of cholesterol, lecithin and glycerides of the fatty acids. Egg oil exhibits activity in regulating the gut microbial dysbiosis, alleviating obesity, insulin resistance and inflammation[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 8001-17-0. Pack Sizes: 25 mg; 50 mg. Product ID: HY-N12670. | |
| Egg PC (60%) | Egg PC (60%). Group: Others. L-α-phosphatidylcholine (Egg, Chicken-60%) (Total Egg Phosphatide Extract); Egg PC (60%). Cat No: PHOZ-245. | |
| Egg PG | BOC Sciences provides high-quality Egg PG for your projects. Alternative Names: PGs (egg); L-α-phosphatidylglycerol (Egg, Chicken) (sodium salt). Grades: ≥98%. CAS No. 383907-64-0. Molecular formula: C40H76NaO10P. Mole weight: 771. | |
| Egg phosphatidylglycerol | Egg phosphatidylglycerol. Synonyms: EPG. CAS No. 383907-64-0. Product ID: PE-0569. Molecular formula: C40H76NaO10P. Mole weight: 782.284. Category: Emulsifier. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0569; Egg phosphatidylglycerol; Emulsifier; C40H76NaO10P; 383907-64-0. UNII: NA. Chemical Name: 1, 2-Diacyl-sn-Glycero-3-Phospho-[1-rac-glycerol]. Grade: Pharmceutical Excipients. Administration route: Intravenous injection. Dosage Form: Intravenous injection. Stability and Storage Conditions: Soluble in chloroform, slightly soluble in ethanol, insoluble in water. This product should be dark, sealed, frozen transportation and storage, avoid storage with strong oxidizing substances. Proper use and preservation of the condition of quality can be guaranteed for three years. Phospholipids can be hydrolyzed in strong acid and base environments, so contact with strong acid or base media should be avoided except for strong oxidizing substances. Commonly used amount and the maximum amount: The maximum dosage of intravenous injection is 0.36mg. |  |
| Egg Phospholipids | Egg Phospholipids. Synonyms: E322; egg lecithin; LSC 5050; LSC 6040; mixed soybean phosphatides; ovolecithin; Phosal 53 MCT; Phospholipon 100 H; ProKote LSC; soybean lecithin; soybean phospholipids; Sternpur; vegetable lecithin. CAS No. 93685-90-6. Product ID: PE-0429. Category: Dispersants; Emollient; emulsifying agent. Product Keywords: Pharmaceutical Excipients; Excipients for Liquid Dosage Form; Egg Phospholipids; Dispersion Excipients; Dispersants; Emollient; emulsifying agent; 93685-90-6; 93685-90-6. UNII: 1Z74184RGV. Chemical Name: Egg yolk lecithin. Grade: Pharmceutical Excipients. Administration route: Intravenous, oral. Dosage Form: Injection, Emulsion, Powder lyophilized, for soultion, Tablet. | |
| Egg SM | Sphingomyelins (SMs) are bioactive sphingolipids found in mammalian cell membranes. Sphingomyelin obtained from natural sources, such as eggs or bovine brain, contains fatty acids of various chain length. Alternative Names: Sphingomyelin (Egg, Chicken); 16:0 SM; Hexadecanoyl Sphingomyelin; N-hexadecanoyl-D-erythro-sphingosylphosphorylcholine. Grades: 98%. CAS No. 383907-87-7. Molecular formula: C39H79N2O6P. Mole weight: 703.03. | |
| Egg Trans PE | Phosphatidylethanolamine (PE) is a phospholipid in all living organism. The egg yolk contains high levels of unsaturated PE which accounts to 83.10%. Alternative Names: L-α-phosphatidylethanolamine, transphosphatidylated (Egg, Chicken). Grades: >99%. CAS No. 383907-63-9. Molecular formula: C39H76NO8P. Mole weight: 717.99. | |
| Egg yolk lecithin | Lecithins vary greatly in their physical form, from viscous semiliquids to powders, depending upon the free fatty acid content. They may also vary in color from brown to light yellow, depending upon whether they are bleached or unbleached or on the degree of purity. When they are exposed to air, rapid oxidation occurs, also resulting in a dark yellow or brown color. Lecithins have practically no odor. Those derived from vegetable sources have a bland or nutlike taste, similar to that of soybean oil. Synonyms: E322; egg lecithin; LSC 5050; LSC 6040; mixed soybean phosphatides; ovolecithin; Phosal 53 MCT; Phospholipon 100 H; ProKote LSC; soybean lecithin; soybean phospholipids; Sternpur; vegetable lecithin. CAS No. 93685-90-6. Product ID: PE-0112. Category: Emollient; Emulsifying Agents; Solubilizing Agents. Product Keywords: Humectants Excipients; Stabilizers; Emulsifier & Suspending Agents; ; PE-0112; Egg yolk lecithin; Emollient; Emulsifying Agents; Solubilizing Agents; ; 93685-90-6. UNII: 1Z74184RGV. Chemical Name: Egg Phospholipids. Grade: Pharmceutical Excipients. Administration route: Intravenous, oral. Dosage Form: Injection, Emulsion, Powder lyophilized, for soultion, Tablet. Stability and Storage Conditions: Lecithins decompose at extreme pH. They are also hygroscopic and subject to microbial degradation. When heated, lecithins oxidize, darken, and decompose. Temperatures of 160-180°C will cause degradatio | |
| Egg Yolk Lecithin | Egg Phosphatide Extract can be used to prevent and treat atherosclerosis. Alternative Names: Lipoid E 100; Lipoid E 75; Lipoid E 80; Lipoid E80S; Lipoid EPC; Nikkol Lecinol Y 10; Nikkol Lecinol Y 10E; Ovothin 120; Ovotin 160; PL 100; PL 100E; PL 100H; PL 100LE; PL 100M; PL 30S; PL 60; Phosphatides, egg yolk; Phospholipon E 80; QPFCPL 100P; Yokuretopauda LP; Yolk lecithin; Yolkin IP Lecithin; Phospholipids egg. CAS No. 93685-90-6. | |
| Egg yolk oil | Egg yolk oil. CAS No. 8001-17-0. | |
| Eghoxylated Bisphenol-A Diacrylate | Eghoxylated Bisphenol-A Diacrylate. | |
| Eglin c(42-45)-methyl ester. hcl | Eglin c(42-45)-methyl ester. hcl. Alternative Names: PRO-VAL-THR-LEU-OME;H-PRO-VAL-THR-LEU-OME HCL;EGLIN C (42-45)-METHYL ESTER;EGLIN C (42-45)-METHYL ESTER. HCL. CAS No. 133463-25-9. Product ID: ACM133463259. Molecular formula: C21H38N4O6.HCl. Mole weight: 442.55. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Eglin c(60-63)-methyl ester | Eglin c(60-63)-methyl ester. Alternative Names: THR-ASN-VAL-VAL-OME;EGLIN C (60-63)-METHYL ESTER;EGLIN C (60-63)-METHYL ESTER ACETATE SALT;H-THR-ASN-VAL-VAL-OME ACETATE SALT;H-THR-ASN-VAL-VAL-OME ACOH;eglin C fragment 60-63 methyl ester;H-Thr-Asn-Val-Val-OMe. CAS No. 131696-94-1. Purity: 96%. Product ID: ACM131696941. Molecular formula: C19H35N5O7. Mole weight: 505.56. IUPAC Name: methyl (2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]-4-oxobutanoyl]amino]-3-methylbutanoyl]amino]-3-methylbutanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| EGLU | EGLU ((2S)-α-Ethylglutamic acid; (2S)-α-EGLU) is a potent and competitive mGluR-2 receptor antagonist. EGLU interacts with (lS,3S)-ACPD-sensitive site with a Kd value of 66 μM. EGLU is an antidepressant agent[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (2S)-α-Ethylglutamic acid; (2S)-α-EGLU. CAS No. 170984-72-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-101332. | |
| Eglumegad | Eglumegad (LY354740) is a highly potent and selective group II (mGlu2/3) receptor agonist with IC50s of 5 nM and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LY354740; Eglumetad. CAS No. 176199-48-7. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg. Product ID: HY-18941. | |
| EGNHS | EGNHS is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EGS crosslinker. CAS No. 70539-42-3. Pack Sizes: 50 mg; 100 mg; 250 mg; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-130458. | |
| EGR-1-IN-1 | EGR-1-IN-1 is a EGR-1 inhibitor with an IC50 of 1.86 μM. EGR-1-IN-1 binds to the zinc finger DNA-binding domain of EGR-1 and promotes the dissociation of the EGR-1-DNA complex. EGR-1-IN-1 reduces the mRNA expression levels of EGR-1-regulated inflammatory genes induced by TNFα. EGR-1-IN-1 alleviates atopic dermatitis-like lesions in the ear skin of mice. EGR-1-IN-1 serves as a lead compound for the development of targeted compounds for inflammatory skin diseases. EGR-1-IN-1 can be used in studies related to atopic dermatitis[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3077196-25-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-163731. | |
| EGT1442 | EGT1442 is a potent and selective SGLT2 inhibitor with IC50 value of 5.6 μM /2 nM in SGLT1 /SGLT2 respectively. It significantly prolonged the median survival of SHRSP rats. It attenuates blood glucose and HbA(1c) levels and prolongs the survival of stroke-prone rats in db/db mice. It showed favorable properties both in vitro and in vivo and could be beneficial to the management of type 2 diabetic patients. It was developed by Theracos and in clinic phase 1 trials. Uses: Egt1442 showed favorable properties and could be beneficial to the management of type 2 diabetic patients. Alternative Names: THR1442; THR-1442; THR 1442; EGT1442; EGT-1442; EGT 1442; Bexagliflozin; (1S)-1,5-Anhydro-1-C-[4-chloro-3-[[4-[2-(cyclopropyloxy)ethoxy]phenyl]methyl]phenyl]-D-glucitol;Bexagliflozin;THR1442;EGT0001442;EGT-1442;THR-1442;EGT-0001442;(2S,4R,6R)-2-(4-chloro-3-(4-(2-cyclopropoxyethoxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol;(3R,4R,5S,6R)-2-(4-chloro-3-(4-(2-cyclopropoxyethoxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. Grades: >98%. CAS No. 1118567-05-7. Molecular formula: C24H29ClO7. Mole weight: 464.94. | |
| EGTA | EGTA is a cell-impermeant specific calcium ion chelator. EGTA has an apparent calcium dissociation constant (Kd) of 60.5 nM at physiological pH (7.4) and has very high specificity for Ca2+ over Mg2+ (Mg2+ Kd 1-10 mM). EGTA significantly inhibits the substrate adherence capacity of inflammatory macrophages[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 67-42-5. Pack Sizes: 500 mg; 1 g; 5 g; 10 g. Product ID: HY-D0861. | |
| EGTA | Chelating agent for the determination of calcium. Group: Biochemicals. Alternative Names: Ethyleneglycol-bis-(2 aminoethylether)-N,N.N,N-tetraacetic acid; Glycol ether diamine tetraacetic acid; Egtazic acid. Grades: Molecular Biology Grade. CAS No. 67-42-5. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C14H24N2O10, Molecular Weight: 380.35. US Biological Life Sciences. |  Worldwide |
| EGTA | 25g Pack Size. Group: Biochemicals, Ligands. Formula: C14H24N2O10. CAS No. 67-42-5. Prepack ID 29346817-25g. Molecular Weight 380.35. See USA prepack pricing. |  |
| EGTA acetoxymethyl ester | EGTA acetoxymethyl ester is a cell-permeant form of EGTA, a calcium chelator. This indicator has been used for detecting intracellular calcium. Alternative Names: EGTA/AM; EGTA AM; EGTA tetra(acetoxymethyl ester). Grades: 95%. CAS No. 99590-86-0. Molecular formula: C26H40N2O18. Mole weight: 668.6. | |
| EGTA-AM | EGTA-AM is a membrane permeable form of EGTA, can be passively loaded into cells to generate intracellular EGTA; EGTA-AM is also a Ca2+ chelator with slow chelating dynamics. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EGTA Acetoxymethyl ester. CAS No. 99590-86-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-D0973. | |
| EGTA tetrasodium | EGTA tetrasodium. Group: Biochemicals. Alternative Names: Ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid tetrasodium salt. Grades: Highly Purified. CAS No. 13368-13-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C14H20N2O10·4Na. US Biological Life Sciences. | Worldwide |
| EGTA tetrasodium | EGTA tetrasodium is a cell-impermeant specific calcium ion chelator. EGTA tetrasodium has an apparent calcium dissociation constant (Kd) of 60.5 nM at physiological pH (7.4) and has very high specificity for Ca2+ over Mg2+ (Mg2+ Kd 1-10 mM). EGTA tetrasodium significantly inhibits the substrate adherence capacity of inflammatory macrophages[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 13368-13-3. Pack Sizes: 10 mM * 1 mL in Water; 500 mg; 1 g. Product ID: HY-D0861A. | |
| EH-IDTBR | EH-IDTBR. Molecular formula: C72H88N6O2S8. Mole weight: 1326g/mol. IUPAC Name: (5Z)-3-ethyl-2-sulfanylidene-5-[[4-[9,9,18,18-tetrakis(2-ethylhexyl)-15-[7-[(Z)-(3-ethyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)methyl]-2,1,3-benzothiadiazol-4-yl]-5,14-dithiapentacyclo[10.6.0.03,10.04,8.013,17]octadeca-1(12),2,4(8),6,10,13(17),15-heptaen-6-yl]-2,1,3-benzothiadiazol-7-yl]methylidene]-1,3-thiazolidin-4-one. SMILES: CCCCC(CC)CC1(C2=CC3=C(C=C2C4=C1C=C(S4)C5=CC=C(C6=NSN=C56)C=C7C(=O)N(C(=S)S7)CC)C(C8=C3SC(=C8)C9=CC=C(C1=NSN=C91)C=C1C(=O)N(C(=S)S1)CC)(CC(CC)CCCC)CC(CC)CCCC)CC(CC)CCCC. InChI: InChI=1S/C72H88N6O2S8/c1-11-21-25-43(15-5)39-71(40-44(16-6)26-22-12-2)53-35-52-54(36-51(53)65-55(71)37-57(83-65)49-31-29-47(61-63(49)75-87-73-61)33-59-67(79)77(19-9)69(81)85-59)72(41-45(17-7)27-23-13-3,42-46(18-8)28-24-14-4)56-38-58(84-66(52)56)50-32-30-48(62-64(50)76-88-74-62)34-60-68(80)78(20-10)70(82)86-60/h29-38,43-46H,11-28,39-42H2,1-10H3/b59-33-,60-34-. | |
| EHMT2-IN-1 | EHMT2-IN-1 is a potent EHMT inhibitor, with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2. Used in the research of blood disorder or cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2230849-55-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111778. | |
| EHMT2-IN-2 | EHMT2-IN-2 is a potent EHMT inhibitor, with IC50s of all <100 nM for EHMT1 peptide, EHMT2 peptide and cellular EHMT2. Used in the research of blood disease or cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2230850-47-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-111904. | |
| EHNA hydrochloride | EHNA hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 81408-49-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| EHNA hydrochloride | EHNA hydrochloride is a potent and selective dual inhibitor of cyclic nucleotide phosphodiesterase 2 (PDE2)(IC50=4 μM) and adenosine deaminase (ADA). EHNA hydrochloride exerts a concentration inhibition of the cGMP-stimulated PDE II (cGs-PDE)(IC50:0.8 μM (human), 2 μM (porcine myocardium)), but has smaller inhibitory effect on the unstimulated PDE2 activity. EHNA hydrochloride play roles in mediating diverse pharmacological responses, including antiviral, antitumour and antiarrhythmic effects[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 58337-38-5. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103160A. | |
| EHNA Hydrochloride (NSC263164, EHNA HCl, Adenosine deaminase inhibitor, 9H-Purine-9-ethanol, monohydrochloride) | EHNA Hydrochloride (NSC263164, EHNA HCl, Adenosine deaminase inhibitor, 9H-Purine-9-ethanol, monohydrochloride). Group: Biochemicals. Alternative Names: (2S,3R)-3-(6-aminopurin-9-yl)nonan-2-ol;hydrochloride. Grades: Highly Purified. CAS No. 58337-38-5. Pack Sizes: 25mg. Molecular Formula: C14 H23 N5, Molecular Weight: 313.8. US Biological Life Sciences. | Worldwide |
| EHop-016 | EHop-016 is a potent and selective Rac GTPase Rac1 and Rac3 inhibitor. EHop-016 inhibits Rac1 activity with an IC50 of 1.1 μM in MDA-MB-435 cells. EHop-016 inhibits Vav2 interaction with Rac, Rac-activated PAK1, lamellipodia formation, and cell migration[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1380432-32-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12810. | |
| Ehp-inhibitor-1 | Ehp-inhibitor-1 is an Eph family tyrosine kinase inhibitor targeting Eph receptors. Study indicated that inhibition of Eph receptors results in an increase in glucose-stimulated insulin secretion from mouse and human pancreatic islets. Alternative Names: 6-(3-methoxyphenyl)-3-pyridin-3-ylpyrazolo[1,5-a]pyrimidin-7-amine. CAS No. 861249-59-4. Molecular formula: C18H15N5O. Mole weight: 317.352. | |
| Ehp-inhibitor-2 | Ehp-inhibitor-2 is an Eph family tyrosine kinase inhibitor targeting Eph receptors. Study indicated that inhibition of Eph receptors results in an increase in glucose-stimulated insulin secretion from mouse and human pancreatic islets. Alternative Names: 3-(7-amino-3-(pyridin-3-yl)pyrazolo[1,5-a]pyrimidin-6-yl)phenol. CAS No. 861249-77-6. Molecular formula: C17H13N5O. Mole weight: 303.325. | |
| EHT 1610 | EHT 1610 is a potent inhibitor of DYRK, with IC50s of 0.36 nM (DYRK1A), 0.59 nM (DYRK1B), respectively. EHT 1610 exhibits antileukemia effect, regulates cell cycle and induces cell apoptosis[1]-[4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1425945-60-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111380. | |
| EHT 1864 | EHT 1864 is an inhibitor of Rac family small GTPases. EHT 1864 directly binds and impairs the ability of this small GTPase to engage critical downstream effectors required for growth transformation. The Kd values are 40, 50, 60, and 230 nM for Rac1, Rac1b, Rac2 and Rac3, respectively. EHT 1864 also potently inhibits other Rac-dependent transformation processes, Tiam1- and Ras-mediated growth transformation. EHT 1864 prevents Aβ 40 and Aβ 42 production in vivo. EHT 1864 dependently suppresses the release of migrasomes from podocytes induced by LPS, PAN, or HG[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 754240-09-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16659. | |
| EHT 5372 | EHT 5372 is a highly potent and selective inhibitor of DYRK's family kinases with IC50s of 0.22, 0.28, 10.8, 93.2, 22.8, 88.8, 59.0, 7.44, and 221 nM for DYRK1A, DYRK1B, DYRK2, DYRK3, CLK1, CLK2, CLK4, GSK-3α, and GSK-3β, respectively[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1425945-63-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-111379. | |
| Ehtyl Alcohol 200 Proof | Ehtyl Alcohol 200 Proof Alternative Name: Ethanol- 200 proof//Denatured Alcohol. Grade: 100%/200 proof. CAS Number: 64-17-5. |  Los Angeles, CA 90023 |
| EI-1507-1 | EI-1507-1 is produced by the strain of Streptomyces sp. E-1507. It had weak antibacterial activity, and it inhibited ICE with an IC50 of 0.23 μmol/L. Molecular formula: C20H18O6. Mole weight: 354.35. | |
| EI-1507-2 | EI-1507-2 is produced by the strain of Streptomyces sp. E-1507. It had weak antibacterial activity, and it inhibited ICE with an IC50 of 0.42 μmol/L. Molecular formula: C20H20O6. Mole weight: 356.37. | |
| EI-1511-3 | It is produced by the strain of Streptomyces sp. E-1511. EI-1511-3 inhibited recombinant human ICE with an IC50 of 0.09 μmol/L. Alternative Names: (2E,4E)-N-[(1S,5S,6R)-5-hydroxy-5-{(1E,3E,5E)-7-[(2-hydroxy-5-oxocyclopent-1-en-1-yl)amino]-7-oxohepta-1,3,5-trien-1-yl}-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-7-methylocta-2,4-dienamide. Molecular formula: C27H30N2O7. Mole weight: 494.54. | |
| EI-1511-5 | It is produced by the strain of Streptomyces sp. E-1511. EI-1511-5 inhibited recombinant human ICE with an IC50 of 0.38 μmol/L. Alternative Names: (2E,4E,6E)-N-[(1S,5S,6R)-5-hydroxy-5-{(1E,3E,5E)-7-[(2-hydroxy-5-oxocyclopent-1-en-1-yl)amino]-7-oxohepta-1,3,5-trien-1-yl}-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-8-methyldeca-2,4,6-trienamide. Molecular formula: C29H32N2O7. Mole weight: 520.57. | |
| EI-1625-2 | It is produced by the strain of Streptomyces sp. E-1625. EI-1625-2 inhibited recombinant human ICE with an IC50 of 0.2 μmol/L. Alternative Names: (2E)-N-[(1S,5R,6R)-5-hydroxy-5-{(1E,3E,5E)-7-[(2-hydroxy-5-oxocyclopent-1-en-1-yl)amino]-7-oxohepta-1,3,5-trien-1-yl}-2-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-4-methyloct-2-enamide. Molecular formula: C27H32N2O7. Mole weight: 496.55. | |
| EI-1941-1 | It is originally isolated from Farrowia sp. E-1941. EI-1941-1 inhibited recombinant human ICE with an IC50 of 0.086 μmol/L. It also inhibits elastase and cathepsin. Alternative Names: 2,3-Dihydroxy-5-propyl-1a,5,6,7a-tetrahydro-2H-oxireno[g]isochromen-7(3H)-one. CAS No. 189828-31-7. Molecular formula: C12H16O5. Mole weight: 240.25. | |
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