Quinolines and derivatives
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Filtered Search Results
Ambeed 1 1 Biphenyl 4ylboronic acid
[1,1'-Biphenyl]-4-ylboronic acid, 5122-94-1, 98%
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Ambeed 1Methylpyrrolidine
1-Methylpyrrolidine, 120-94-5, 95%
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Ambeed 5Amino2methoxypyrimidine
5-Amino-2-methoxypyrimidine, 56621-89-7, 98%
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Selleck Chemical LLC SH-4-54
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SH-4-54 is a potent STAT inhibitor with KD of 300 nM and 464 nM for STAT3 and STAT5 respectively
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Ambeed 2 4DibromoN 4bromophenyl N 2 4
2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline, 73087-81-7, 95%
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Ambeed R 2Amino3 4fluorophenyl propa
(R)-2-Amino-3-(4-fluorophenyl)propanoic acid, 18125-46-7, 98%
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Ambeed 2 4DibromoN 4bromophenyl N 2 4
2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline, 73087-81-7, 95%
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Ambeed 1 Benzyloxy 4iodo1Hpyrazole
1-(Benzyloxy)-4-iodo-1H-pyrazole, 229171-07-7, 95%
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TARGETMOL CHEMICALS INC Pinocembrin 7-O-3 -O-galloyl-4
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Also available in 1 mg, 10 mg and bulk. Please contact Fisher for quotes. Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-beta-D-glucoside can moderately inhibit alpha-amylase activity, with an IC50 value of 0.03 µmol/ml. Purity 98.73%
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Ambeed 3 2Hydroxyethoxy propanoic aci
3-(2-Hydroxyethoxy)propanoic acid, 89211-34-7, 95%
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Ambeed 1R 2S 1Amino2 3dihydro1Hinden
(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol, 136030-00-7, 98%
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Ambeed 3Chloro4methoxybenzaldehyde
3-Chloro-4-methoxybenzaldehyde, 4903-09-7, 98%
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Ambeed 4 Benzyloxy phenyl boronic ac
(4-(Benzyloxy)phenyl)boronic acid, 146631-00-7, 98%
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![Medchemexpress LLC 6-[2-[4-[(4-fluorophenyl)phenylmethylene]-1-piperidinyl]ethyl]-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one | 93076-89-2 | MFCD00055114 | 99.8% | 459.58 g·mol⁻¹ | C27H26FN3OS | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000241481.png-250.jpg)
Medchemexpress LLC 6-[2-[4-[(4-fluorophenyl)phenylmethylene]-1-piperidinyl]ethyl]-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one | 93076-89-2 | MFCD00055114 | 99.8% | 459.58 g·mol⁻¹ | C27H26FN3OS | 100 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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R 59-022 is a small-molecule diacylglycerol kinase (DGK) inhibitor used in biochemical and cell-based studies to probe DAG/PKC signaling and lipid metabolism. It also functions as a 5-HT receptor antagonist and activates protein kinase C, potentiating thrombin-induced diacylglycerol production in platelets.
- Inhibits diacylglycerol kinase activity (IC50 ~2.8 μM).
- Acts as a 5-HT receptor antagonist and activates protein kinase C.
- Modulates diacylglycerol and phosphatidic acid metabolism in cells.
- High purity suitable for biochemical assays and cell studies.
- Offered in solid and solution formats for flexible experimental use.
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![Apexbio Technology LLC prostate apoptosis response protein PAR-4 (2-7) [Homo sapiens] 1mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000096894.png-250.jpg)
Apexbio Technology LLC prostate apoptosis response protein PAR-4 (2-7) [Homo sapiens] 1mg
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Prostate apoptosis response protein PAR-4 2-7 is a short peptide targeting transcriptional regulation pathways It is designed to modulate transcription factor activity thereby influencing apoptosis mechanisms particularly in prostate cells PAR-4 2-7 exerts its biological activity primarily through interaction with transcription factors via a leucine zipper zinc finger domain facilitating apoptosis in transformed or malignant cells while sparing normal cells Based on these properties PAR-4 2-7 holds research potential in studies investigating tumor suppression mechanisms and transcription-mediated apoptosis regulation in oncology and therapeutic research
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