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| Product | Description | |
|---|---|---|
| Eletriptan | Eletriptan is Serotonin 1D receptor agonist originated by Pfizer. It is a second generation triptan drug. It is used as an abortive medication, blocking a migraine attack which is already in progress. Eletriptan was approved by the FDA for the acute treatment of migraine with or without aura in adults in 2002. Uses: Menstrual migraine; migraine. Synonyms: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole; (R)-5-[2-(Benzenesulfonyl)ethyl]-3-[(N-methylpyrrolidin-2-yl)methyl]-1H-indole; Eletriptan; UK 116044; UK-116,044; UK-116,044-04 [as hydrobromide]; UNII-22QOO9B8KI; Relpax free amine. Grade: 98%. CAS No. 143322-58-1. Molecular formula: C22H26N2O2S. Mole weight: 382.52. |  |
| Eletriptan-[d3] | Eletriptan-[d3], is the labelled analogue of Eletriptan, which is a serotonin 5-HTIB/ID receptor agonist. Eletriptan is a second generation triptan medication intended for treatment of migraine headaches. Synonyms: Eletriptan-d3; 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole-d3; 3-{[(2R)-1-(2H3)Methyl-2-pyrrolidinyl]methyl}-5-[2-(phenylsulfonyl)ethyl]-1H-indole. Grade: 95% by HPLC; 95% atom D. CAS No. 1287040-94-1. Molecular formula: C22H23D3N2O2S. Mole weight: 385.54. | |
| Eletriptan-d3 hydrobromide | Eletriptan-d3 is used as an internal standard for the quantification of eletriptan by GC- or LC-MS. Eletriptan is an agonist of the serotonin (5-HT) receptor types 5-HT1B and 5-HT1D. Synonyms: UK 116044-d3; 3-[[(2R)-1-methyl-d3-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole, monohydrobromide. Grade: ≥99% atom D. Molecular formula: C22H23D3N2O2S·HBr. Mole weight: 466.45. | |
| Eletriptan HBr | Eletriptan induces concentration-dependent contractions of meningeal artery, coronary artery, and saphenous vein. The potency of Eletriptan is higher in meningeal artery than in coronary artery (86-fold) or saphenous vein (66-fold). Synonyms: Eletriptan Hydrobromide; CHEBI:61176; M41W832TA3; UNII-M41W832TA3; eletriptan hydrobromide; Relpax; UK 166,044; UK 166044; UK-166,044; UK-166044. Grade: >98%. CAS No. 177834-92-3. Molecular formula: C22H26N2O2S.HBr. Mole weight: 463.43. | |
| Eletriptan hydrobromide | Eletriptan hydrobromide. Group: Biochemicals. Grades: Highly Purified. CAS No. 177834-92-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. |  Worldwide |
| Eletriptan hydrobromide | Eletriptan hydrobromide. CAS No. 17783-49-2. Purity: 96%. Product ID: ACM17783492. Molecular formula: C11H20O2. Mole weight: 462.42. IUPAC Name: undec-10-enoicacid. ECNumber: 203-965-8. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Eletriptan N-oxide | An impurity of Eletriptan. Synonyms: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole N Oxide. Grade: > 95%. CAS No. 1217641-89-8. Molecular formula: C22H26N2O3S. Mole weight: 398.53. | |
| Eletriptan N-Oxide | An impurity of Eletriptan. Group: Biochemicals. Alternative Names: 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole N Oxide. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Eleutherin | Eleutherin is a type of naphthoquinone derivative with the protective effect against the injury ofhuman umbilical vein endothelial cells (HUVECs), which can be isolated from the edible bulbs of Eleutherine americana (Hong-Cong)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: (+)-Eleutherin. CAS No. 478-36-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N8248. |  |
| Eleutherococcus Senticosus Liquid Extract | Eleutherococcus Senticosus Liquid Extract. |  CA, FL & NJ |
| Eleuthero Extract | Eleuthero Root Extract (also known as siberian ginseng root extract ) is prepared from the root of the plant Siberian Ginseng, it has been traditionally used to negate stress and fatigue. The active ingredients of eleuthero root extract, also known as acanthopanax senticosus extract is eleutherosides. Siberian ginseng root extract is used to increase stamina and to stimulate the immune system and used for conditions of the heart and blood vessels such as high blood pressure, low blood pressure, and atherosclerosis. Group: Others. Mole weight: 742.72. Eleuthero Extract; Eleutherococcus Sentisosus. Cat No: EXTC-042. |  |
| Eleutheroside A | Daucosterol can be used as an efficient and inexpensive neuroprotectant, to which the IGF1-like activity of Daucosterol contributes. Daucosterol could be potentially developed as a medicine for ischemic stroke treatment. Uses: Analgesic. Synonyms: Daucosterol; Sitogluside; Alexandrin; beta-Sitosterol glucoside; Daucosterin; Coriandrinol. Grade: >98%. CAS No. 474-58-8. Molecular formula: C35H60O6. Mole weight: 576.85. | |
| Eleutheroside A | Eleutheroside A. Group: Biochemicals. Alternative Names: Daucosterol; Alexandrin; Daucosterin; Sitogluside. Grades: Plant Grade. CAS No. 474-58-8. Pack Sizes: 20mg. Molecular Formula: C35H60O6, Molecular Weight: 576.847. US Biological Life Sciences. | Worldwide |
| Eleutheroside B | Eleutheroside B. Group: Biochemicals. Alternative Names: Syringin; Lilacin; Methoxyconiferin; Magnolenin A; Alyposide; Syringoside; Ligustrin; Ilexanthin A. Grades: Plant Grade. CAS No. 118-34-3. Pack Sizes: 20mg. Molecular Formula: C17H24O9, Molecular Weight: 372.367. US Biological Life Sciences. | Worldwide |
| Eleutheroside C | Eleutheroside C is isolated from the root barks of Eleutherococcus senticosus. Synonyms: ethyl alpha-d-galactopyranoside. Grade: > 95%. CAS No. 15486-24-5. Molecular formula: C8H16O6. Mole weight: 208.2. | |
| Eleutheroside D | Botanical Source: Group: Biochemicals. Grades: Plant Grade. CAS No. 79484-75-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Eleutheroside E | Eleutheroside E. Group: Biochemicals. Alternative Names: Acanthoside D; Syringaresinol-di-O-glucoside. Grades: Plant Grade. CAS No. 39432-56-9. Pack Sizes: 20mg. Molecular Formula: C34H46O18, Molecular Weight: 742.718. US Biological Life Sciences. | Worldwide |
| Eleutheroside E | Eleutheroside E is an important component of ginseng that can be taken orally. Eleutheroside E has anti-inflammatory and antioxidant properties, and it helps reduce apoptosis in heart cells caused by hypoxia-reoxygenation (H/R) damage. Eleutheroside E can improve type 2 diabetes, enhance cognitive function, and has neuroprotective effects[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 39432-56-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0272. | |
| Elevenostat | Elevenostat (JB3-22) is a selective HDAC11 inhibitor with an IC50 of 0.235 μM. Elevenostat can induce apoptosis of multiple myeloma cells and has anti-tumor effect. In addition, Elevenostat inhibits the maturation of mouse oocytes[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: JB3-22. CAS No. 1454902-97-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145757. | |
| Elexacaftor | Elexacaftor (VX-445)is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector. It promotes the processing and trafficking of CFTR, increases the amount of CFTR on the cell surface, and improves the processing and trafficking of Phe508del CFTR protein. Category: Active pharmaceutical ingredients. CAS No. 2216712-66-0. Product ID: API2216712660. Molecular formula: C26H34F3N7O4S. Mole weight: 597.65. |  |
| Elexacaftor | Elexacaftor (VX-445, Compound 1) is a modulator of cystic fibrosis transmembrane conductance regulator (CFTR). Elexacaftor (VX-445, Compound 1) facilitates the processing and trafficking of CFTR to increase the amount of CFTR at the cell surface[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: VX-445. CAS No. 2216712-66-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111772. | |
| Elexacaftor | Elexacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector used as a medication for cystic fibrosis treatment in combination with ivacaftor and tezacaftor. Synonyms: VX-445; VX445; (S)-N-((1,3-dimethyl-1H-pyrazol-4-yl)sulfonyl)-6-(3-(3,3,3-trifluoro-2,2-dimethylpropoxy)-1H-pyrazol-1-yl)-2-(2,2,4-trimethylpyrrolidin-1-yl)nicotinamide. Grade: 98%. CAS No. 2216712-66-0. Molecular formula: C26H34F3N7O4S. Mole weight: 597.65. | |
| Elezanumab | Elezanumab (ABT-555; AE12-1Y-QL) is a human monoclonal antibody that selectively targets repulsive guidance molecule A (RGMa). Elezanumab potently inhibited RGMa mediated BMP signalling via the SMAD1/5/8 pathway, with an IC50 around 97 pM. Elezanumab promotes neuroregeneration and neuroprotection in neuronal injury and demyelination models binds N-terminal RGMa, blocks BMP signaling and lacks RGMc cross-reactivity. elezanumab has neuroregenerative and neuroprotective activities without impact on iron metabolism[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ABT-555; AE12-1Y-QL; Anti-RGMA Reference Antibody (elezanumab). CAS No. 1791416-49-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99359. | |
| Elf18 | Elf18 is a peptide fragment of bacterial translation elongation factor Tu (EF-Tu). Elf18 can be recognized by plant pattern recognition receptors, thereby inducing an immune response. Elf18 can enhance plants' resistance to pathogens and can be used in research related to plant immune responses[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 849352-44-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P10396. | |
| Elgemtumab | Elgemtumab(LJM716) is a fully human IgG monoclonal antibody. Elgemtumab can specifically bind to HER3, block ligand-dependent and independent HER3 signal transduction and cell proliferation, and has good anti-tumor potential[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LJM716. CAS No. 1512559-37-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99936. | |
| EL-HPE High Performance Electrolyte | EL-HPE High Performance Electrolyte. Alternative Names: EL-HPE electrolyte,EL-HPE. |  |
| EL-HSE High Stability Electrolyte | EL-HSE High Stability Electrolyte. Alternative Names: EL-HSE electrolyte,EL-HSE. | |
| EL-HTE High Temperature Electrolyte | EL-HTE High Temperature Electrolyte. | |
| Eliapixant | Eliapixant is a P2X3 receptor antagonist, which is under a clinical trial for refractory chronic cough (RCC) treatment. Synonyms: BAY 1817080. CAS No. 1948229-21-7. Molecular formula: C22H21F3N4O3S. Mole weight: 478.49. | |
| Eliapixant | Eliapixant (BAY 1817080) is a potent and selective antagonist of P2X3 receptor, with an IC50 of 8 nM. Eliapixant can be used for the research of refractory chronic cough[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY 1817080. CAS No. 1948229-21-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109170. | |
| Eliglustat | Eliglustat is a glucosylceramide synthase inhibitor used for the long-term treatment of type 1 Gaucher disease. Category: Active pharmaceutical ingredients. Synonyms: Genz-99067. Genz 99067. GENZ-112638. CAS No. 491833-29-5. Product ID: API491833295. Molecular formula: C23H36N2O4. Mole weight: 404.5. SMILES: CCCCCCCC(=O)NC(CN1CCCC1)C(C2=CC3=C(C=C2)OCCO3)O. Appearance: Solid powder. | |
| Eliglustat | Eliglustat is a glucosylceramide synthase inhibitor indicated for the long-term treatment of type 1 Gaucher disease in patients who are CYP2D6 extensive metabolizers, intermediate metabolizers , or poor metabolizers in treatment-naive and treatment-experi. Uses: Inhibits glucosylceramide synthase(gcs). Synonyms: Genz-99067; Genz 99067; Genz99067; N-[(1R,2R)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]octanamide. Grade: ≥98%. CAS No. 491833-29-5. Molecular formula: C23H36N2O4. Mole weight: 404.55. | |
| Eliglustat | Eliglustat is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Genz 99067. CAS No. 491833-29-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14885. | |
| Eliglustat hemitartrate | Eliglustat hemitartrate is a specific inhibitor of glucosylceramide synthase. It is under development as an oral substrate reduction therapy for Gaucher disease type 1 (GD1). It was developed by Genzyme Corp and has been listed by the FDA August 2014. Synonyms: Genz-112638; Genz 112638; Genz112638; Eliglustat tartrate; Bis(N-((1R,2R)-2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2-hydroxy-1-(pyrrolidin-1- ylmethyl)ethyl)octanamide) (2R,3R)-2,3-dihydroxybutanedioate; Octanamide, N-((1R,2R)-2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-hydroxy-1-(1- pyrrolidinylmethyl)ethyl)-, (2R,3R)-2,3-dihydroxybutanedioate; N-[(1R,2R)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]octanamide (2R,3R)-2,3-dihydroxybutanedioic acid. Grade: >98%. CAS No. 928659-70-5. Molecular formula: C50H78N4O14. Mole weight: 959.17. | |
| Eliglustat hemitartrate | Eliglustat hemitartrate is an specific, potent and orally active glucocerebroside synthase inhibitor with an IC50 of 24 nM. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Genz-112638; Eliglustat tartrate. CAS No. 928659-70-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-14885A. | |
| Eliglustat Impurity 1 | Eliglustat Impurity 1. Uses: For analytical and research use. Alternative Names: (1R,2R)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-(((S)-2-hydroxy-1-phenylethyl)amino)-3-(pyrrolidin-1-yl)propan-1-ol. CAS No. 491833-27-3. Molecular formula: C23H30N2O4. Mole weight: 398.5. Catalog: APB491833273. |  |
| Eliglustat Impurity 2 | Eliglustat Impurity 2. Uses: For analytical and research use. Alternative Names: 1-((2R,3R)-3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-hydroxy-2-octanamidopropyl)pyrrolidine 1-oxide. CAS No. 2137145-62-9. Molecular formula: C23H36N2O5. Mole weight: 420.54. Catalog: APB2137145629. | |
| Eliglustat Impurity 3 | Eliglustat Impurity 3. Uses: For analytical and research use. Alternative Names: (2S,3R)-3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-hydroxy-2-(((S)-2-hydroxy-1-phenylethyl)amino)-1-(pyrrolidin-1-yl)propan-1-one. CAS No. 491833-26-2. Molecular formula: C23H28N2O5. Mole weight: 412.48. Catalog: APB491833262. | |
| Eliglustat Impurity 4 | Eliglustat Impurity 4. Uses: For analytical and research use. Alternative Names: (1R,2R)-2-amino-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyrrolidin-1-yl)propan-1-ol. Molecular formula: C15H22N2O3. Mole weight: 278.35. Catalog: APB05846. | |
| Eliglustat Impurity 5 | Eliglustat Impurity 5. Uses: For analytical and research use. Alternative Names: N-((1S,2S)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-hydroxy-3-(pyrrolidin-1-yl)propan-2-yl)octanamide. CAS No. 1092472-70-2. Molecular formula: C23H36N2O4. Mole weight: 404.54. Catalog: APB1092472702. | |
| Eliglustat Impurity 6 | Eliglustat Impurity 6. Uses: For analytical and research use. Alternative Names: N-((1S,2R)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-hydroxy-3-(pyrrolidin-1-yl)propan-2-yl)octanamide. CAS No. 1092472-66-6. Molecular formula: C23H36N2O4. Mole weight: 404.54. Catalog: APB1092472666. | |
| Elimusertib | Elimusertib (BAY-1895344) is a potent, orally active and selective ATR inhibitor with an IC50 of 7 nM. Elimusertib has anti-tumor activity[1][2]. Elimusertib can be used for the research of solid tumors and lymphomas[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BAY 1895344. CAS No. 1876467-74-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101566. | |
| Elinafide | Elinafide, an isoquinoline derivative, has been found to be a Type II DNA topoisomerase inhibitor that was once developed in anticancer studies. Synonyms: Elinafide; UNII-HL580335SI; Elinafide [INN]; 2-[2-[3-[2-(1,3-dioxobenzo[de]isoquinolin-2-yl)ethylamino]propylamino]ethyl]benzo[de]isoquinoline-1,3-dione; LU-79553. Grade: 98%. CAS No. 162706-37-8. Molecular formula: C31H28N4O4. Mole weight: 520.59. | |
| Elinogrel | Elinogrel. Group: Biochemicals. Grades: Purified. CAS No. 936500-94-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Elinogrel | Elinogrel is a P2Y12 antagonist displaying antiplatelet activity. Synonyms: 5-Chloro-N-[[[4-[6-Fluoro-1,4-dihydro-7-(methylamino)-2,4-dioxo-3(2H)-quinazolinyl]phenyl]amino]carbonyl]-2-thiophenesulfonamide. Grade: ≥98% by HPLC. CAS No. 936500-94-6. Molecular formula: C20H15ClFN5O5S2. Mole weight: 523.95. | |
| Elintaal | Elintaal (Acetaldehyde Ethyl Linalyl Acetal). CAS No. 40910-49-4. VIGON Item # 503213. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Elinzanetant | Elinzanetant is a neurokinin receptors antagonist that may help reduce the frequency and severity of hot flushes during menopause. Elinzanetant reduces Estradiol and Progesterone in Healthy Women. Synonyms: BAY 3427080; BAY-3427080; BAY3427080; NT 814; NT-814; NT814; GSK1144814A; GSK-1144814A; GSK 1144814A. Grade: 98%. CAS No. 929046-33-3. Molecular formula: C33H35F7N4O3. Mole weight: 668.66. | |
| Elinzanetant | Elinzanetant is an orally active and selective NK-1 and NK-3 receptor antagonist. Elinzanetant alleviates menopause-associated vasomotor symptoms, including hot flashes and night sweats. Elinzanetant reduces estradiol and progesterone levels. Elinzanetant can be used for the research of moderate to severe vasomotor and sleep disorders associated with menopause[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NT-814; BAY3427080. CAS No. 929046-33-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109171. | |
| Elipovimab | Elipovimab is a potent broadly neutralizing HIV-1 antibody for the targeted elimination of HIV-infected cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2101210-43-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99937. | |
| Eliprodil | Eliprodil. Group: Biochemicals. Grades: Purified. CAS No. 119431-25-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Eliprodil | Eliprodil, a NR2B-NMDA receptor antagonist, was found to have neuroprotective activity in study of ischemia. Uses: Eliprodil is a nr2b-nmda receptor antagonist that was found to have neuroprotective activity in study of ischemia. Synonyms: -(4-Chlorophenyl)-4-[(4-fluorophenyl)methyl]-1-piperidineethanol, SL-82,0715; SL82,0715; SL 82,0715; SL-820715; SL820715; SL 820715; Eliprodil. Grade: 95%. CAS No. 119431-25-3. Molecular formula: C20H23ClFNO. Mole weight: 347.85. | |
| Elironrasib | Elironrasib is an orally active and covalent inhibitor of KRASG12C(ON). Elironrasib forms a tri-complex within tumor cells between KRASG12C(ON) and cyclophilin A (CypA). Thus, Elironrasib prevents KRASG12C(ON) from signaling via steric blockade of RAS effector binding. Elironrasib inhibits ERK signaling and induced apoptosis in KRASG12C-mutant H358 cells. Elironrasib also inhibits the proliferation of KRASG12C mutant cells with a median IC50 of 0.11 nM[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RMC-6291. CAS No. 2641998-63-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153346. | |
| elisabethatriene synthase | Requires Mg2+ or less efficiently Mn2+. The enzyme is also able to use farnesyl diphosphate and geranyl diphosphate. Group: Enzymes. Synonyms: elisabethatriene cyclase. Enzyme Commission Number: EC 4.2.3.41. CAS No. 334022-59-2. 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-5200; elisabethatriene synthase; EC 4.2.3.41; 334022-59-2; elisabethatriene cyclase. Cat No: EXWM-5200. | |
| Elisartan | Elisartan, also known as HN-65021, is an orally active non-peptide prodrug of angiotensin II AT1 receptor antagonist HN-12206, and shows anti-hypertension activities. Uses: Angiotensin ii type 1 receptor blockers. Synonyms: 1H-Imidazole-5-carboxylic acid, 2-butyl-4-chloro-1-((2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl)methyl)-, 1-((ethoxycarbonyl)oxy)ethyl ester; HN 65021; HN-65021. CAS No. 149968-26-3. Molecular formula: C27H29ClN6O5. Mole weight: 553.01. | |
| Elisidepsin | Elisidepsin is a marine-derived, synthetic cyclic depsipeptide with potential antineoplastic activity. Elisidepsin is a derivative of a natural marine compound that belongs to a family of dehydro aminobutyric acid-containing peptides (kahalalides) isolated from the herbivorous marine mollusk Elysia rufescens. Although the primary mechanism of action has yet to be elucidated, this agent exhibits anti-proliferative activity in a wide variety of cancer cell types, including breast, colon, pancreas, lung, and prostate; it appears to induce oncolytic rather than apoptotic cell death. Synonyms: PM-02734; N-[(4S)-4-methylhexanoyl]-D-valyl-L-threonyl-L-valyl-D-valyl-D-prolyl-L-ornithyl-N-{(3S,6Z,9S,12R,15R,18R,19R)-9-benzyl-15-[(2S)-butan-2-yl]-6-ethylidene-3,12-diisopropyl-19-methyl-2,5,8,11,14,17-hexaoxo-1-oxa-4,7,10,13,16-pentaazacyclononadecan-18-yl}-D-alloisoleucinamide. CAS No. 681272-30-0. Molecular formula: C75H124N14O16. Mole weight: 1477.90. | |
| Elismetrep | Elismetrep (MT-8554) is a TRPM8 antagonist. Elismetrep reduces the frequency of vasomotor symptoms. Elismetrep can be used for study of pain[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MT-8554. CAS No. 1400699-64-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109087. | |
| Elisrasib | Elisrasib (D3S-001) is an orally active and selective inhibitor for KRAS. Elisrasib inhibits the proliferation of KRASG12C mutant H358 and MIA-PA-CA-2. D3S-001 also inhibits the phosphorylation of cellular ERK1/2. Elisrasib exhibits good metabolic stability in hepatocytes, liver microsomes, plasma and whole blood in various species. D3S-001 exhibits good pharmacokinetic characteristics and antitumor efficacy in mice[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: D3S-001. CAS No. 2914919-85-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-160023. | |
| Elizabethin | It is produced by the strain of Streptomyces elizabethii. It has antifungal activity. CAS No. 78361-81-6. Molecular formula: C35H58O12. Mole weight: 670.83. | |
| Ellagic acid | 25g Pack Size. Group: Aroma Chemicals, Biochemicals, Flavours and Fragrance Materials. Formula: C14H6O8. CAS No. 476-66-4. Prepack ID 23304412-25g. Molecular Weight 302.19. See USA prepack pricing. |  |
| Ellagic acid | Ellagic acid. Synonyms: 4,4',5,5',6,6'-Hexahydroxydiphenic acid 2,6,2',6'-dilactone, Alizarin Yellow, Benzoaric acid, Elagostasine, Eleagic acid, Gallogen, Lagistase. CAS No. 476-66-4. Product ID: CDC10-0049. Molecular formula: C14H6O8 xH2O. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Ellagic acid; CDC10-0049; 476-66-4; C14H6O8 xH2O; 4,4',5,5',6,6'-Hexahydroxydiphenic acid 2,6,2',6'-dilactone, Alizarin Yellow, Benzoaric acid, Elagostasine, Eleagic acid, Gallogen, Lagistase; 207-508-3; MFCD00006914; 476-66-4. Purity: ≥95% (HPLC). Color: Tan to gray. EC Number: 207-508-3. Physical State: Powder. Solubility: 1 M NaOH: 10 mg/mL. Quality Level: 200. Storage: 2-8°C. Boiling Point: 363.24°C (rough estimate). Melting Point: ≥350 °C. Density: 1.667 g/mL. |  |
| Ellagic acid | Ellagic acid appears as cream-colored needles (from pyridine) or yellow powder. Odorless. (NTP, 1992);Solid. Alternative Names: Eleagicacid. CAS No. 476-66-4. Molecular formula: C14H6O8. Mole weight: 302.19. Purity: 98%. IUPAC Name: 6,7,13,14-Tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione. SMILES: C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O. InChI: InChI=1S/C14H6O8/c15-5-1-3-7-8-4(14(20)22-11(7)9(5)17)2-6(16)10(18)12(8)21-13(3)19/h1-2,15-18H. | |
| Ellagic acid | Ellagic acid is a natural phenol antioxidant found in numerous fruits and vegetables. The antiproliferative and antioxidant properties of ellagic acid have prompted research into its potential health benefits. It has been fraudulently marketed as having the ability to prevent and treat a number of human maladies, including cancer, but such claims have not been proven. Ellagic acid can be used in cosmetics material. Uses: Anti-proliferative; anti-oxidant. Synonyms: Elagostasine, Gallogen; Alizarine Yellow; Benzoaric acid; CCRIS 774; CCRIS774; CCRIS-774; HSDB 7574; HSDB7574; HSDB-7574; Lagistase. Grade: >98%. CAS No. 476-66-4. Molecular formula: C14H6O8. Mole weight: 302.19. | |
| Ellagic acid | Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive inhibitor of CK2 and SHP2, with an IC50 of 40 nM and a Ki of 20 nM. Uses: Scientific research. Category: Signaling pathways. CAS No. 476-66-4. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0183. | |
| Ellagic Acid | Ellagic Acid is a phenol antioxidant found naturally in various fruits and vegetables. Ellagic Acid was shown to exhibit high levels of antiproliferative and antioxidant properties in studies, which suggests its potential health benefits following ellagic acid consumption. Group: Biochemicals. Alternative Names: Alizarin yellow; Alizarine Yellow; Benzoaric acid; C.I. 55005; C.I. 75270; Elagostasine; Eleagic acid; G 91006; Gallogen; Gallogen (astringent); LDN 0097519; Lagistase. Grades: Highly Purified. CAS No. 476-66-4. Pack Sizes: 25g. Molecular Formula: C??H?O?, Molecular Weight: 302.19. US Biological Life Sciences. | Worldwide |
| Ellagic Acid | Ellagic Acid. CAS No. 476-66-4. Purity: 40%. Product ID: CI-NAT-476664. Molecular formula: C14H6O8. Mole weight: 302.28 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ellagic acid 7-O-beta-D-xylopyranoside-2,3,8-trimethyl ether | Ellagic acid 7-O-beta-D-xylopyranoside-2,3,8-trimethyl ether. CAS No. 136133-08-9. Product ID: ACM136133089. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ellagic acid, 96% | Ellagic acid appears as cream-colored needles (from pyridine) or yellow powder. Odorless. (NTP, 1992);Solid. CAS No. 476-66-4. Molecular formula: C14H6O8. Mole weight: 302.19g/mol. IUPAC Name: 6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione. SMILES: C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O. InChI: InChI=1S/C14H6O8/c15-5-1-3-7-8-4(14(20)22-11(7)9(5)17)2-6(16)10(18)12(8)21-13(3)19/h1-2,15-18H. | |
| Ellagic acid dihydrate | Ellagic acid dihydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 133039-73-3. Pack Sizes: 100mg, 250mg. Molecular Formula: C14H6O8.2H2O, Molecular Weight: 338.223. US Biological Life Sciences. | Worldwide |
| ELLIPTICINE | Ellipticine is a DNA intercalating agent and a DNA topoisomerase II inhibitor. Ellipticine is also a natural product, isolated in 1959 from the Australian evergreen tree of the Apocynaceae family. Ellipticine was found to be an extremely promising anticancer drug. The planar polycyclic structure was found to interact with DNA through intercalation, exhibiting a high DNA binding affinity (10(6) M(-1)). The presence of protonatable ring nitrogens distinguished ellipticine from other simple intercalators. Both monocationic and uncharged species were found to be present under physiological conditions. The positive charge stabilized the binding of ellipticine to nucleic acids, while the more lipophilic uncharged compound was shown to readily penetrate membrane barriers. The structural nature of these compounds offers a plausible basis for the implication of multiple modes of action, including DNA binding, interactions with membrane barriers, oxidative bioactivation and modification of enzyme function; most notably that of topoisomerase II and telomerase. (Curr Med Chem Anticancer Agents. 2004 Mar;4(2):149-72). Synonyms: BRN 0221300; CCG-36483; CCRIS 2003; DB-052047; elliptecine; ellipticine; Elliptisine; K00071; LP00531; LS-133282; NSC 71795; NSC71795; NSC-71795; TCMDC-125546; VZ29809. Grade: 0.98. CAS No. 519-23-3. Molecular formula: C17H14N2. Mole weight: 246.31. | |
| Ellipticine hydrochloride | Ellipticine is a DNA intercalating agent and a DNA topoisomerase II inhibitor. Ellipticine is a natural product isolated from the Australian evergreen tree of the Apocynaceae family. Synonyms: NSC 71795 hydrochloride; Ellipticine HCl; PZE. CAS No. 5081-48-1. Molecular formula: C17H15ClN2. Mole weight: 282.77. | |
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