Aminophenols
eMolecules 548-37-8 | Medchem Express | Verbenalin | 5mg | 523883500 | HY-N2014 | MFCD00017414 | 388.369 | C17H24O10
Medchem Express | Verbenalin | 5mg | 523883500 | HY-N2014 | 548-37-8 | MFCD00017414 | 388.369 | C17H24O10
Cayman Chemical N-formyl-2-AmInophenol 500mg
A bacterial secondary metabolite with antioxidant activity; scavenges DPPH radicals in a cell-free assay (IC50 = 3.23 UG/ml); has been used in the synthesis of compounds with antibacterial and antifungal activities
eMolecules 2-(4-Tolyl)-4-(4-hydroxyphenyl)thiazole | 1500577-50-3 | MFCD27919676 | 1g
Oakwood Chemical | 2-(4-Tolyl)-4-(4-hydroxyphenyl)thiazole | 1g | 537706252 | 098246 | | 1500577-50-3 | MFCD27919676 | 267.350 | C16H13NOS
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eMolecules Building Block Tool
Ambeed 2Methoxy6 trifluoromethoxy ph
(2-Methoxy-6-(trifluoromethoxy)phenyl)boronic acid, 309977-92-2, 95%
Selleck Chemical LLC 3-Hydroxybenzoic acid
3-Hydroxybenzoic acid (m-Hydroxybenzoic acid 3-Carboxyphenol m-Salicylic acid) is used as an intermediate in the synthesis of plasticisers resins pharmaceuticals etc
TARGETMOL CHEMICALS INC TC-S 7005 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. TC-S 7005 is an effective inhibitor of Polo-like kinases (IC50s 214 nM 4 nM and 24 nM for Plk1 Plk2 and Plk3). purity: 99%
TARGETMOL CHEMICALS INC ABT530 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. ABT530 (Pibrentasvir) is an HCV NS5A inhibitor with EC50s ranging from 1.4-5.0 pM against HCV replicons containing NS5A from genotypes 1-6. purity: 99%
TARGETMOL CHEMICALS INC SMARCA-BD LIGAND 1 FOR P 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. SMARCA-BD ligand 1 for Protac is a compound capable of binding to SMARCA2 the BAF ATPase subunit based on the Protac technology for degrading SMARCA2purity: 100%
eMolecules 303986-05-2 | 3-Chloro-N-(3-hydroxyphenyl)-2,2-dimethylpropanamide | Oakwood Chemical | MFCD00793397 | 227.690 | C11H14ClNO2 | 99.000 | CC(C)(CCl)C(=O)Nc1cccc(O)c1 | 100mg | 537712736
3-Chloro-N-(3-hydroxyphenyl)-2,2-dimethylpropanamide | Oakwood Chemical | 303986-05-2 | MFCD00793397 | 227.690 | C11H14ClNO2 | 99.000 | CC(C)(CCl)C(=O)Nc1cccc(O)c1 | 100mg | 537712736
Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 100 MG
UNC9994 hydrochloride is a functionally selective, β-arrestin-biased dopamine D2 receptor (D2R) agonist that selectively activates β-arrestin recruitment and signaling. It shows a binding affinity with a Ki of 79 nM for D2R. UNC9994 hydrochloride is also an antagonist of Gi-regulated cAMP production and a partial agonist for D2R/β-arrestin-2 interactions. It demonstrates antipsychotic-like activity. It is for research use only.
- Functions as a β-arrestin-biased dopamine D2 receptor agonist.
- Selectively activates β-arrestin recruitment and signaling.
- Exhibits a binding affinity (Ki) of 79 nM for D2R.
- Acts as an antagonist of Gi-regulated cAMP production.
- Serves as a partial agonist for D2R/β-arrestin-2 interactions.
- Demonstrates antipsychotic-like activity.
Medchemexpress LLC SKI V | 10 MG
SKI V is a noncompetitive and potent non-lipid sphingosine kinase (SPHK; SK) inhibitor with an IC50 of 2 μM for GST-hSK. It potently inhibits PI3K with an IC50 of 6 μM for hPI3k. SKI V decreases the formation of the mitogenic second messenger sphingosine-1-phosphate (S1P), induces apoptosis, and exhibits antitumor activity.
- Noncompetitive and potent non-lipid sphingosine kinase (SPHK; SK) inhibitor.
- Inhibits PI3K.
- Decreases formation of sphingosine-1-phosphate (S1P).
- Induces apoptosis.
- Possesses antitumor activity.
Biotang Inc Fenretinide, > 99%, 50MG, 4-HPR;MK-4016;McN-R-1967;RII retinamide;Ro 22-4667. M.W. 391.55, C26H33NO2, 65646-68-6.
Fenretinide, > 99%, 50MG, 4-HPR;MK-4016;McN-R-1967;RII retinamide;Ro 22-4667. M.W. 391.55, C26H33NO2, 65646-68-6.
=O | 1g | 482599101](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502441437.PNG-250.jpg)
eMolecules 119-34-6 | 4-AMINO-2-NITROPHENOL | AstaTech | MFCD00007876 | 154.125 | C6H6N2O3 | 95.000 | Nc1ccc(O)c(c1)[N+]([O-])=O | 1g | 482599101
4-AMINO-2-NITROPHENOL | AstaTech | 119-34-6 | MFCD00007876 | 154.125 | C6H6N2O3 | 95.000 | Nc1ccc(O)c(c1)[N+]([O-])=O | 1g | 482599101
Medchemexpress LLC MK-3207 hydrochloride | 957116-20-0 | MFCD16038934 | 98.1% | 594.05 g/mol | C31H30ClF2N5O3 | 1 ML
MK-3207 Hydrochloride is a potent, orally bioavailable CGRP receptor antagonist used in research on CGRP-mediated signaling and migraine-related pathways. It exhibits sub-nanomolar potency and high selectivity versus related receptors, and is provided in solution and solid forms for laboratory use.
- Potent CGRP receptor antagonist with IC50 0.12 nM and Ki 0.024 nM.
- Highly selective versus AM1, AM2, CTR, and AMY3 receptors.
- Available as a 10 mM solution (1 mL) and as solid quantities for preparation.
- Purity approximately 98.1% by analytical methods.
- Molecular formula C31H30ClF2N5O3; molecular weight 594.05 g/mol.
- Provided with structural identifiers to support research (SMILES, PubChem CID).