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Filtered Search Results
Medchemexpress LLC Sec61-IN-1 (compound A317) | 2484865-42-9 | 99.7% | 430.53 g/mol | C23H22N6OS | 5 MG
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Sec61-IN-1 (compound A317) is a small-molecule inhibitor of the Sec61 translocon used as a research tool to study protein translocation and Sec61-mediated pathways. Manufacturer documentation reports molecular formula C23H22N6OS, molecular weight 430.53 g/mol, and purity of 99.7%. The compound has been reported to target glioma cells and to enhance T cell cytotoxic effects in experimental studies.
- High purity (99.7%) suitable for research use.
- Selective inhibition of Sec61-mediated protein translocation.
- Reported activity against glioma cells and enhancement of T cell cytotoxicity.
- Supplied as a five mg vial for small-scale in vitro or in vivo preparation.
- Includes supporting documentation: data sheet, certificate of analysis, and safety data sheet.
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Medchemexpress LLC HY-17512A 5g , Losartan (potassium) DuP-753 potassium CAS:124750-99-8 Purity:98%
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Medchemexpress, HY-17512A 5g Losartan (potassium) DuP-753 potassium CAS:124750-99-8 Formula:C22H22ClKN6O IC50: 20 nM (angiotensin II) Purity:98% Losartan (potassium) is an angiotensin II receptor antagonist, competing with the binding of angiotensin II to AT1 receptors with IC 50 of 20 nM. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1803274-65-8 | Medchem Express | BAY-1436032 | 5mg | 446254848 | HY-100020 | 489.539 | C26H30F3N3O3
Medchem Express | P053 | 5mg | 713705994 | HY-126015 | 2748196-63-4 | 354.270 | C18H21Cl2NO2
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Medchemexpress LLC YM-244769 | 838819-70-8 | 99.2% | 443.47 | 50 MG
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YM-244769 is a potent, selective, and orally active Na+/Ca2+ exchanger (NCX) inhibitor. It preferentially inhibits NCX3 and suppresses the unidirectional outward NCX current (Ca2+ entry mode) with IC50s of 18 nM and 50 nM, respectively. It efficiently protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage and can increase urine volume and urinary excretion of electrolytes in mice.
- Potent, selective, and orally active Na+/Ca2+ exchanger (NCX) inhibitor.
- Preferentially inhibits NCX3 (IC50 = 18 nM).
- Suppresses unidirectional outward NCX current (Ca2+ entry mode) with an IC50 of 50 nM.
- Efficiently protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage.
- Increases urine volume and urinary excretion of electrolytes in mice.
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Sigma Aldrich Fine Chemicals Biosciences Candesartan cilexetil Related Compound D United States Pharmacopeia (USP) Reference Standard | 1185256-03-4 | 10MG
Candesartan cilexetil Related Compound D United States Pharmacopeia (USP) Reference Standard | Mol Wt: 610.66 | 1185256-03-4 | 10MG
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eMolecules 34308-25-3 | 1-Methyladenosine hydroiodide | Combi-Blocks | MFCD00058140 | 409.184 | C11H16IN5O4 | 95.000 | I.Cn1cnc2n(cnc2c1=N)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 1g | 303331780
1-Methyladenosine hydroiodide | Combi-Blocks | 34308-25-3 | MFCD00058140 | 409.184 | C11H16IN5O4 | 95.000 | I.Cn1cnc2n(cnc2c1=N)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O | 1g | 303331780
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eMolecules 104227-86-3 | ChemScene | Famciclovir USP impurity A | 100mg | 642097326 | CS-0181544 | MFCD00870146 | 237.263 | C10H15N5O2
Medchem Express | Gepotidacin | 1mg | 446267800 | HY-16742 | 1075236-89-3 | MFCD27987926 | 448.527 | C24H28N6O3
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eMolecules 479065-00-4 | (S)-3-(P-METHYLPHENYL)-BETA-ALANINE | AstaTech | MFCD03840388 | 179.219 | C10H13NO2 | 97.000 | Cc1ccc(cc1)[C@@H](N)CC(O)=O | 5g | 112528010
(S)-3-(P-METHYLPHENYL)-BETA-ALANINE | AstaTech | 479065-00-4 | MFCD03840388 | 179.219 | C10H13NO2 | 97.000 | Cc1ccc(cc1)[C@@H](N)CC(O)=O | 5g | 112528010
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eMolecules 2140-71-8 | 2'-O-Methylguanosine | Broadpharm297.271 | C11H15N5O5 | 0.000 | CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c1[nH]c(N)nc2=O | 1g | 761707715
2'-O-Methylguanosine | Broadpharm | 2140-71-8297.271 | C11H15N5O5 | 0.000 | CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c1[nH]c(N)nc2=O | 1g | 761707715
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Medchemexpress LLC Calmidazolium chloride | 57265-65-3 | MFCD00077679 | 99.9% | 687.70 | C31H23Cl7N2O
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Calmidazolium chloride is a calmodulin antagonist supplied as a research reagent for in vitro biochemical studies. It is used to inhibit calmodulin-dependent enzymes and calcium-transport processes; reported identifiers include CAS 57265-65-3, molecular formula C31H23Cl7N2O, and molecular weight 687.70.
- Calmodulin antagonist with high affinity binding to CaM (reported Kd ≈ 3 nM).
- Inhibits CaM-dependent phosphodiesterase and CaM-induced activation of Ca2+ transport (reported IC50s ≈ 0.15 and 0.35 μM).
- High reported purity in manufacturer COA (example batch: LCMS 99.94%).
- Supplied as a solid research chemical with storage recommendations to keep sealed and away from moisture.
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Aobchem AOBCHEM
5001032523 METHYL 2-ETHOXYPYRIDINE-3-CARB
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Ambeed AMBEED
5000949289 2-BORONOTHIOPHENE-3-CARB 100MG
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Sigma Aldrich Fine Chemicals Biosciences Olmesartan medoxomil European Pharmacopoeia (EP) Reference Standard | 144689-63-4 | MFCD00944911 |
Olmesartan medoxomil European Pharmacopoeia (EP) Reference Standard | Mol Wt: 558.59 | 144689-63-4 | MFCD00944911 |
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eMolecules 7720-39-0 | 2-Aminoimidazole | Accela ChemBio | MFCD00792530 | 83.094 | C3H5N3 | 95.000 | Nc1ncc[nH]1 | 10g | 811174510
2-Aminoimidazole | Accela ChemBio | 7720-39-0 | MFCD00792530 | 83.094 | C3H5N3 | 95.000 | Nc1ncc[nH]1 | 10g | 811174510
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eMolecules 1187931-38-9 | (4-Amino-butyl)-methyl-carbamic acid tert-butyl ester oxalate | J & W PharmLab, LLC | MFCD11858337 | 292.332 | C12H24N2O6 | 96.000 | OC(=O)C(O)=O.CN(CCCCN)C(=O)OC(C)(C)C | 5g | 250001627
(4-Amino-butyl)-methyl-carbamic acid tert-butyl ester oxalate | J & W PharmLab, LLC | 1187931-38-9 | MFCD11858337 | 292.332 | C12H24N2O6 | 96.000 | OC(=O)C(O)=O.CN(CCCCN)C(=O)OC(C)(C)C | 5g | 250001627
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