Azoles
Medchemexpress LLC HY-17039 10mg Medchemexpress, Alcaftadine CAS:147084-10-4 Purity:>98%
Medchemexpress, HY-17039 10mg Alcaftadine CAS:147084-10-4 Alcaftadine (R89674) is a histamine H1 receptor antagonist, which is used to prevent eye irritation brought on by allergic conjunctivitis. Alcaftadine is a broad-spectrum antihistamine displaying a high affinity for histamine H1 and H2 receptors and a lower affinity for H4 receptors. Alcaftadine also exhibits modulatory action on immune cell recruitment and mast cell stabilizing effects. 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.
eMolecules 14357-08-5 | Medchem Express | N6-Ethyladenosine | 10mg | 451965711 | HY-111809 | 295.299 | C12H17N5O4
Ambeed | 6-Chloro-1H-indole-3-carbonitrile | 250mg | 598444251 | A737290 | 194490-17-0 | MFCD07776605 | 176.600 | C9H5ClN2
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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
Selleck Chemical LLC BIA 10-2474
BIA 10-2474 is a novel fatty acid amide hydrolase (FAAH) inhibitor with a potent inhibitory effect upon FAAH and prolonged action in vivo
Selleck Chemical LLC NG 52
NG-52 is a tri-substituted purine that binds to the ATP-binding site of yeast cyclin-dependent kinases inhibiting Cdc28p and Pho85p with IC50s of 7 and 2 M respectively
Medchemexpress LLC 1H-Imidazole, 1-dodecyl- | 4303-67-7 | 99.78% | 236.40 | 1 ML
1H-Imidazole, 1-dodecyl- | 4303-67-7 | 99.78% | 236.40 | 1 ML
Sigma Aldrich Fine Chemicals Biosciences Olmesartan medoxomil British Pharmacopoeia (BP) Reference Standard | 144689-63-4 | MFCD00944911 |
Olmesartan medoxomil British Pharmacopoeia (BP) Reference Standard | Mol Wt: 558.59 | 144689-63-4 | MFCD00944911 |
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
eMolecules 65039-05-6 | 1-Butyl-3-methylimidazolium iodide | MFCD08276307 | 25g
Ambeed | 1-Butyl-3-methylimidazolium iodide | 25g | 552640159 | A199824 | 65039-05-6 | MFCD08276307 | 266.126 | C8H15IN2
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Medchemexpress LLC 4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)phenyl)picolinamide | 1262041-49-5 | Not listed | 99.6% | 411.46 | C23H21N7O | 25 MG
GS-444217 is a selective, orally available ATP-competitive inhibitor of apoptosis signal-regulating kinase 1 (ASK1). It exhibits potent in vitro inhibition (IC50 2.87 nM) and has reported in vivo activity in rodent kidney (in vivo EC50 ≈ 1.6 μM; activity observed at 30 mg/kg). The compound is supplied as a research-grade powder.
- Selective ATP-competitive ASK1 inhibitor.
- Potent in vitro activity: IC50 2.87 nM.
- Demonstrated in vivo activity in rodent kidney (in vivo EC50 ≈ 1.6 μM).
- Supplied as a powder for research use.
- Molecular formula C23H21N7O; molecular weight 411.46.
- CAS number 1262041-49-5.
Medchemexpress LLC Rad16-I hydrochloride | 2100275-49-6 | 98.9% | 10 MG
RAD16-I hydrochloride is a soft nanofibrous self-assembling peptide. It provides a suitable microenvironment for the proliferation and differentiation of human mesenchymal stem cells (hMSC) into chondrocytes. It is also an ionic complementary peptide that has been used as a model to investigate the potential amyloid-like staining properties of Self-Assembling Peptide Nanofibers (SAPNFs).
- Provides a suitable microenvironment for human mesenchymal stem cells' (hMSC) proliferation and differentiation into chondrocytes.
- Used to check potential amyloid-like staining properties of SAPNFs.
Medchemexpress LLC HY-17505 1g , Candesartan (Cilexetil) TCV-116 CAS:145040-37-5 Purity:98%
Medchemexpress, HY-17505 1g Candesartan (Cilexetil) TCV-116 CAS:145040-37-5 Formula:C33H34N6O6 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.
Medchemexpress LLC Ym-244769 (hydrochloride) | 837424-39-2 | MFCD31561984 | 99.0% | 479.93 g/mol | C26H23ClFN3O3 | 50 MG
YM-244769 hydrochloride is a potent, selective inhibitor of the Na+/Ca2+ exchanger (NCX) supplied as a high-purity research chemical for pharmacological and physiological studies. The product is provided as a hydrochloride salt in powder form and is used in cardiovascular and neurological research to probe NCX-mediated transport and signaling.
- Potent, selective inhibition of Na+/Ca2+ exchanger for NCX studies.
- High purity suitable for in vitro and in vivo research.
- Provided as a stable hydrochloride salt for reproducible dosing.
- Supplied as a powder for flexible formulation and storage.
- Documented certificate of analysis and safety data sheet available for quality assurance.
Medchemexpress LLC Upacicalcet sodium | 2052969-18-1 | 99.9% | 373.75 | 1 ML
Upacicalcet sodium is a non-peptide calcimimetic agent that functions as a calcium-sensing receptor (CaSR) agonist. It is used in secondary hyperparathyroidism (SHPT) research due to its ability to decrease serum intact parathyroid hormone (iPTH) and calcium (Ca2+) levels, which helps reduce hypocalcemia and gastrointestinal complications. This compound also improves vascular calcification and bone disorders in models of adenine-induced SHPT and inhibits cortical pore formation and bone fibrosis in rats with chronic kidney disease (CKD).
- Functions as a CaSR agonist (EC50 = 10.8 nM)
- Increases intracellular Ca2+ and IP-1 in human CaSR-expressing cells
- Reduces serum iPTH, Ca2+, and Pi levels in rats
- Inhibits parathyroid hyperplasia in CKD rat models
- Inhibits ectopic calcification and cortical hole formation in CKD rat models
eMolecules 25743-12-8 | NH-bis(PEG2-OH) | Broadpharm | MFCD29764330 | 281.349 | C12H27NO6 | 98.000 | OCCOCCOCCNCCOCCOCCO | 1g | 303671216
NH-bis(PEG2-OH) | Broadpharm | 25743-12-8 | MFCD29764330 | 281.349 | C12H27NO6 | 98.000 | OCCOCCOCCNCCOCCOCCO | 1g | 303671216