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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Candesartan cilexetil United States Pharmacopeia (USP) Reference Standard | 145040-37-5 | MFCD00871371 | 100MG
Candesartan cilexetil United States Pharmacopeia (USP) Reference Standard | Mol Wt: 610.66 | 145040-37-5 | MFCD00871371 | 100MG
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eMolecules Azilsartan | 147403-03-0 | MFCD20278186 | 1g
Combi-Blocks | Azilsartan | 1g | 401038096 | QA-3478 | 98.000 | 147403-03-0 | MFCD20278186 | 456.458 | C25H20N4O5
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Medchemexpress LLC YM-244769 hydrochloride | 837424-39-2 | 99.0% | 479.93 g·mol⁻1 | C26H23ClFN3O3 | 5 MG
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YM-244769 hydrochloride is a potent, selective, and orally active Na+/Ca2+ exchanger (NCX) inhibitor used in preclinical research. It preferentially inhibits NCX3 with low-nanomolar activity and has demonstrated neuroprotective effects in cell models and effects on urine volume and electrolyte excretion in animal studies.
- Potent, selective inhibition of Na+/Ca2+ exchanger (NCX3) with low-nanomolar potency.
- Orally active pharmacology suitable for in vivo preclinical studies.
- Demonstrated neuroprotective activity in hypoxia/reoxygenation cell models.
- Shown to increase urine volume and electrolyte excretion in animal studies.
- Provided as a high-purity solid with recommended cold storage for stability.
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Medchemexpress LLC DiABZI-C2-NH2 | 2137975-93-8 | 96.14% | 721.81 | 100 MG
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diABZI-C2-NH2 is an active analogue containing a primary amine functionality and acts as a STING agonist. It has shown strong anti-tumor activity in immunocompetent mice with syngeneic colon tumors, leading to complete and lasting regression of tumors. This compound can be covalently immobilized on sepharose beads for affinity-capture of potential target proteins from THP1 cell lysate.
- Functions as a STING agonist
- Exhibits strong anti-tumor activity in immunocompetent mice
- Leads to complete and lasting regression of tumors
- Can be covalently immobilized on sepharose beads
- Useful for affinity-capture of potential target proteins from THP1 cell lysate
- Enhanced binding to STING and cellular function
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Medchemexpress LLC YM-244769 dihydrochloride | 1780390-65-9 | 516.39 | 50 MG
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YM-244769 dihydrochloride 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). This compound efficiently protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage and increases urine volume and urinary excretion of electrolytes in mice.
- Potent and selective Na+/Ca2+ exchanger (NCX) inhibitor
- Preferentially inhibits NCX3 with an IC50 of 18 nM
- Suppresses unidirectional outward NCX current (Ca2+ entry mode)
- Protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage
- Increases urine volume and urinary excretion of electrolytes in mice
- Also inhibits NCX1 (IC50: 68 nM) and NCX2 (IC50: 96 nM)
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eMolecules 146894-16-8 | Guanosine 5'-phosphate disodium salt hydrate | MFCD00151238 | 25g
Medchem Express | BCH | 50mg | 559839399 | HY-108540 | 20448-79-7 | 155.197 | C8H13NO2
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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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![eMolecules 303048-33-1 | 1-Methyl-3-[2,3,4-trihydroxy-1-(2-phenylhydrazin-1-ylidene)butyl]-1,2-dihydroquinoxalin-2-one | Oakwood Chemicals368.393 | C19H20N4O4 | 90.000 | Cn1c2ccccc2nc(\C(=N/Nc2ccccc2)C(O)C(O)CO)c1=O | 1mg | 532150617](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502143475.JPG-250.jpg)
eMolecules 303048-33-1 | 1-Methyl-3-[2,3,4-trihydroxy-1-(2-phenylhydrazin-1-ylidene)butyl]-1,2-dihydroquinoxalin-2-one | Oakwood Chemicals368.393 | C19H20N4O4 | 90.000 | Cn1c2ccccc2nc(\C(=N/Nc2ccccc2)C(O)C(O)CO)c1=O | 1mg | 532150617
1-Methyl-3-[2,3,4-trihydroxy-1-(2-phenylhydrazin-1-ylidene)butyl]-1,2-dihydroquinoxalin-2-one | Oakwood Chemicals | 303048-33-1368.393 | C19H20N4O4 | 90.000 | Cn1c2ccccc2nc(\C(=N/Nc2ccccc2)C(O)C(O)CO)c1=O | 1mg | 532150617
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Medchemexpress LLC HY-112843 10mg Medchemexpress, CNT2 inhibitor-1 CAS:880155-70-4 Purity:>98%
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Medchemexpress, HY-112843 10mg CNT2 inhibitor-1 CAS:880155-70-4 CNT2 inhibitor-1 is a potent concentrative nucleoside transporter 2 Inhibitor (CNT2), with an IC50 of 640 nM for hCNT2. Purity:>98% 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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c1ccc(Cl)cc1 | 1g | 112525513](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502171248.JPG-250.jpg)
eMolecules 1213362-28-7 | (R)-3-(4-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | MFCD07784070 | 185.650 | C9H12ClNO | 97.000 | N[C@H](CCO)c1ccc(Cl)cc1 | 1g | 112525513
(R)-3-(4-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | 1213362-28-7 | MFCD07784070 | 185.650 | C9H12ClNO | 97.000 | N[C@H](CCO)c1ccc(Cl)cc1 | 1g | 112525513
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Medchemexpress LLC Losartan carboxylic acid | 124750-92-1 | MFCD00871928 | 99.5% | 436.89 | C22H21ClN6O2 | 5 MG
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Losartan carboxylic acid (E-3174) is the active carboxylic acid metabolite of losartan and a non-peptide angiotensin II type 1 (AT1) receptor antagonist. Supplied as a solid, high-purity reference standard, it is intended for research use in pharmacology, metabolite identification, and analytical method development.
- High-purity solid reference suitable for analytical assays and QC.
- Active AT1 receptor antagonist metabolite used in pharmacology studies.
- Useful for metabolite identification and compound characterization.
- Available in small milligram pack sizes for research applications.
- Molecular formula C22H21ClN6O2 and molecular weight 436.89 g/mol.
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Medchemexpress LLC Tenofovir amibufenamide | 1571076-26-0 | 99.7% | C22H31N6O5P | 10MG
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Tenofovir amibufenamide is an orally active tenofovir prodrug used in antiviral research to inhibit hepatitis B virus (HBV). It is applied in preclinical studies of chronic hepatitis B to evaluate tenofovir-based antiviral activity and pharmacology.
- Orally active tenofovir prodrug suitable for in vivo and in vitro studies.
- Demonstrated inhibition of hepatitis B virus replication.
- Used in chronic hepatitis B research applications.
- High purity (99.7%).
- Molecular formula C22H31N6O5P, molecular weight 490.49 g/mol.
- Available in small research-scale quantities for preclinical use.
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![eMolecules 51036-79-4 | 2-(2-IMIDAZOLYL)ETHANOL | AstaTech | MFCD06655989 | 112.132 | C5H8N2O | 97.000 | OCCc1ncc[nH]1 | 1g | 248473110](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502170804.JPG-250.jpg)
eMolecules 51036-79-4 | 2-(2-IMIDAZOLYL)ETHANOL | AstaTech | MFCD06655989 | 112.132 | C5H8N2O | 97.000 | OCCc1ncc[nH]1 | 1g | 248473110
2-(2-IMIDAZOLYL)ETHANOL | AstaTech | 51036-79-4 | MFCD06655989 | 112.132 | C5H8N2O | 97.000 | OCCc1ncc[nH]1 | 1g | 248473110
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![eMolecules 79917-90-1 | 1-Butyl-3-methylimidazolium chloride | Chem-Impex | MFCD03095425 | 174.670 | C8H15ClN2 | 99.000 | [Cl-].CCCCn1cc[n+](C)c1 | 25g | 386904207](https://assets.fishersci.com/TFS-Assets/CCG/product-images/501717616.jpg-250.jpg)
eMolecules 79917-90-1 | 1-Butyl-3-methylimidazolium chloride | Chem-Impex | MFCD03095425 | 174.670 | C8H15ClN2 | 99.000 | [Cl-].CCCCn1cc[n+](C)c1 | 25g | 386904207
1-Butyl-3-methylimidazolium chloride | Chem-Impex | 79917-90-1 | MFCD03095425 | 174.670 | C8H15ClN2 | 99.000 | [Cl-].CCCCn1cc[n+](C)c1 | 25g | 386904207
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NP(=O)(CO[C@H](C)Cn1cnc2c(N)ncnc12)Oc1ccccc1 | 5g | 388699863](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502180258.JPG-250.jpg)
eMolecules 379270-37-8 | TENOFOVIR ALAFENAMIDE | AstaTech476.474 | C21H29N6O5P | 95.000 | CC(C)OC(=O)[C@H](C)NP(=O)(CO[C@H](C)Cn1cnc2c(N)ncnc12)Oc1ccccc1 | 5g | 388699863
TENOFOVIR ALAFENAMIDE | AstaTech | 379270-37-8476.474 | C21H29N6O5P | 95.000 | CC(C)OC(=O)[C@H](C)NP(=O)(CO[C@H](C)Cn1cnc2c(N)ncnc12)Oc1ccccc1 | 5g | 388699863
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