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Filtered Search Results
Aobchem AOBCHEM
5000921100 ALLYL 2 6-DIFLUOROPHENYL SULFA
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Aobchem 2-(3 4-Difluorophenyl)pyridine | ≥95% | CAS 387831-85-8 | C11H7F2N | 250mg
2-(3 4-Difluorophenyl)pyridine | ≥95% | CAS 387831-85-8 | C11H7F2N | 250mg
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Aobchem (2-Bromo-4 5-difluorophenyl)(methyl)sulfane | ≥97% | CAS 1432609-87-4 | C7H5BrF2S | 1g
(2-Bromo-4 5-difluorophenyl)(methyl)sulfane | ≥97% | CAS 1432609-87-4 | C7H5BrF2S | 1g
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Aobchem (2-Bromo-4 5-difluorophenyl)(methyl)sulfane | ≥97% | CAS 1432609-87-4 | C7H5BrF2S | 500mg
(2-Bromo-4 5-difluorophenyl)(methyl)sulfane | ≥97% | CAS 1432609-87-4 | C7H5BrF2S | 500mg
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Ambeed AMBEED
5000888184 13-BISS-4-S-SEC-BUTYL-45 250MG
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Aobchem AOBCHEM
5000911378 5-FLUORO-2-METHOXY-4- METHYLTH
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![eMolecules 2415163-55-0 | [2-(tert-Butoxycarbonylamino)-7-fluoro-1,3-benzothiazol-4-yl]boronic acid | Combi-Blocks, Inc.312.120 | C12H14BFN2O4S | 98.000 | CC(C)(C)OC(=O)Nc1nc2c(ccc(F)c2s1)B(O)O | 1g | 686216158](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000164726.jpg-250.jpg)
eMolecules 2415163-55-0 | [2-(tert-Butoxycarbonylamino)-7-fluoro-1,3-benzothiazol-4-yl]boronic acid | Combi-Blocks, Inc.312.120 | C12H14BFN2O4S | 98.000 | CC(C)(C)OC(=O)Nc1nc2c(ccc(F)c2s1)B(O)O | 1g | 686216158
[2-(tert-Butoxycarbonylamino)-7-fluoro-1,3-benzothiazol-4-yl]boronic acid | Combi-Blocks, Inc. | 2415163-55-0312.120 | C12H14BFN2O4S | 98.000 | CC(C)(C)OC(=O)Nc1nc2c(ccc(F)c2s1)B(O)O | 1g | 686216158
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Medchemexpress LLC a-Methyltyrosine methyl ester (hydrochloride) | 7361-31-1 | 98.91% | 245.71 | 25 MG
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α-Methyltyrosine methyl ester hydrochloride is an orally active and competitive tyrosine hydroxylase inhibitor. It inhibits the conversion of tyrosine to dopamine and can be used as a tool for sympathetic nervous system research. In rats, it has been observed to cause kidney damage and urethral calculi.
- Orally active.
- Competitive tyrosine hydroxylase inhibitor.
- Inhibits the conversion of tyrosine to dopamine.
- Can be used as a tool for sympathetic nervous system research.
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Apexbio Technology LLC TH-302 918633-87-1 50mg
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TH-302 (CAS 918633-87-1) is a hypoxia-activated prodrug comprising a 2-nitroimidazole moiety linked to a brominated isophosphoramide mustard Under severe hypoxic conditions (approximately 0 1% O ) TH-302 undergoes bioreductive activation releasing the cytotoxic alkylating agent Br-IPM selectively within hypoxic tumor microenvironments In vitro studies demonstrate markedly increased cytotoxicity against tumor cell lines under hypoxia with IC50 values ranging from 0 1 to 0 8 M for H460 Caki-1 SK-MEL-5 DU145 and HCT116 cells while IC50 values exceed 40 M in normoxic conditions In H460 xenograft mouse models TH-302 induces dose-dependent tumor growth inhibition without hematological toxicity and increases H2AX-positive cells indicating DNA damage TH-302 is utilized to investigate tumor hypoxia-targeting therapies and mechanisms of selective cytotoxicity
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Medchemexpress LLC (4-(Thiazol-2-ylcarbamoyl)piperidine-1-carbonyl)-L-leucine | 1814897-92-1 | 99.6% | 368.45 | 5 MG
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This chemical compound, (4-(Thiazol-2-ylcarbamoyl)piperidine-1-carbonyl)-L-leucine, is designed for laboratory use and the manufacture of substances. It is stable under recommended storage conditions and offers high purity.
- High purity of 99.64%
- Suitable for laboratory applications
- Stable under recommended storage conditions
- Not classified as a hazardous substance or mixture
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![Medchemexpress LLC 4-[2-(2-fluorophenyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl]pyridine | 1784751-19-4 | MFCD29924749 | 99.9% | 333.33 g/mol | C20H13F2N3 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215151.png-250.jpg)
Medchemexpress LLC 4-[2-(2-fluorophenyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl]pyridine | 1784751-19-4 | MFCD29924749 | 99.9% | 333.33 g/mol | C20H13F2N3 | 50 MG
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TA-02 is a small-molecule p38 MAPK inhibitor used in biochemical and cell-based research. As an analog of SB 203580, it exhibits potent activity (IC50 ≈ 20 nM) and preferential inhibition of TGFBR-2. The compound is supplied as a high-purity solid suitable for laboratory studies involving kinase signaling modulation.
- Potent p38 MAPK inhibition (IC50 ≈ 20 nM).
- Preferential inhibition of TGFBR-2.
- High purity solid suitable for research applications.
- Compact pack sizes available for small-scale studies.
- Molecular weight ~333.33 g/mol; formula C20H13F2N3.
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![Medchemexpress LLC 4-(2-(4-(benzyloxy)phenyl)acetamido)-1-(3'-chloro-[1,1'-biphenyl]-4-carbonyl)piperidine-4-COOH | 100.0% | 583.07 g/mol | C34H31ClN2O5 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000287705.png-250.jpg)
Medchemexpress LLC 4-(2-(4-(benzyloxy)phenyl)acetamido)-1-(3'-chloro-[1,1'-biphenyl]-4-carbonyl)piperidine-4-COOH | 100.0% | 583.07 g/mol | C34H31ClN2O5 | 10 MG
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YL-365 is a small-molecule GPR34 agonist used in preclinical research on pain and cancer. It has molecular formula C34H31ClN2O5, a molecular weight of 583.07 g/mol, and an analytical purity of 99.96%. The compound is supplied as a solid in milligram quantities and should be stored at 4°C protected from light; in solvent, store at -80°C for up to 6 months or -20°C for up to 1 month.
- Acts as a GPR34 agonist to probe lysophosphatidylserine receptor signaling.
- Suitable for pain and cancer preclinical studies.
- High analytical purity for consistent experimental outcomes.
- Available in small milligram quantities for dosing flexibility.
- Stable when stored under recommended conditions and protected from light.
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Medchemexpress LLC Met kinase-IN-2 | 2101241-90-9 | 98.4% | 50 MG
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MET kinase-IN-2 is a potent, selective, and orally bioavailable MET kinase inhibitor with an IC50 of 7.4 nM. It exhibits antitumor activity.
- Potent and selective MET kinase inhibitor
- Orally bioavailable
- Exhibits antitumor activity
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eMolecules 38862-24-7 | 2,5-Dioxopyrrolidin-1-yl acrylate | Ambeed | MFCD00078261 | 169.136 | C7H7NO4 | 97.000 | C=CC(=O)ON1C(=O)CCC1=O | 25g | 552526338
2,5-Dioxopyrrolidin-1-yl acrylate | Ambeed | 38862-24-7 | MFCD00078261 | 169.136 | C7H7NO4 | 97.000 | C=CC(=O)ON1C(=O)CCC1=O | 25g | 552526338
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eMolecules 224311-51-7 | JOHNPHOS | AstaTech | MFCD01862440 | 298.410 | C20H27P | 98.000 | CC(C)(C)P(c1ccccc1-c1ccccc1)C(C)(C)C | 5g | 392629757
JOHNPHOS | AstaTech | 224311-51-7 | MFCD01862440 | 298.410 | C20H27P | 98.000 | CC(C)(C)P(c1ccccc1-c1ccccc1)C(C)(C)C | 5g | 392629757
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