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Filtered Search Results
eMolecules 2242464-44-2 | Medchem Express | BAY 2416964 | 5mg | 527574132 | HY-135829 | 387.82 | C18H18ClN5O3
ChemScene | (S)-1-(4-(tert-Butyl)phenyl)ethan-1-amine | 100mg | 569143593 | CS-0000313 | 511256-37-4 | MFCD06762044 | 177.291 | C12H19N
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Medchemexpress LLC PND-1186 hydrochloride | 1356154-94-3 | 99.9% | 537.96 | 50 MG
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PND-1186 hydrochloride is a potent, highly-specific, and reversible inhibitor of FAK with an IC50 of 1.5 nM. It selectively promotes tumor cell apoptosis.
- Potent, highly-specific, and reversible FAK inhibitor.
- IC50 of 1.5 nM for FAK.
- Selectively promotes tumor cell apoptosis.
- Inhibits FAK Tyr-397 phosphorylation in breast carcinoma cells.
- Reduces tumor growth by inducing apoptosis in vivo.
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Selleck Chemical LLC Telaglenastat
Telaglenastat (CB-839) is a potent selective and orally bioavailable glutaminase inhibitor with IC50 of 24 nM for recombinant human GAC CB-839(Telaglenastat) inudces autophagy and has antitumor activity Phase 1
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eMolecules 1781835-13-9 | Medchem Express | RN-1 (dihydrochloride) | 5mg | 686240167 | HY-110130 | 452.42 | C23H31Cl2N3O2
Ambeed | (3aS8aR)-2-(Pyrimidin-2-yl)-88a-dihydro-3aH-indeno[12-d]oxazole | 50mg | 600830090 | A1363630 | 2634687-67-3 | 237.262 | C14H11N3O
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![Medchemexpress LLC 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232148.png-250.jpg)
Medchemexpress LLC 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 50 MG
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CCG-100602 is a research-grade small-molecule inhibitor of myocardin-related transcription factor A/serum response factor (MRTF-A/SRF) signaling, supplied as a solid for laboratory research applications.
- Inhibits MRTF-A/SRF signaling and reduces MRTF-A nuclear localization.
- High analytical purity suitable for research use.
- Available in small-scale packages for in-lab assays and dose-response studies.
- Solid form with storage recommendations to protect from light; in solvent store at -80°C for long-term stability.
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eMolecules 138786-67-1 | Medchem Express | Pantoprazole (sodium) | 100mg | 446268552 | HY-17507A | MFCD09852812 | 405.35 | C16H14F2N3NaO4S
Pharmablock | tert-butyl N-(2-oxoazepan-3-yl)carbamate | 25mg | 778477209 | PBTEN15225 | 179686-45-4 | MFCD02183574 | 228.292 | C11H20N2O3
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Selleck Chemical LLC BLU9931-5mg
BLU9931 is a potent, selective, and irreversible FGFR4 inhibitor with IC50 of 3 nM, about 297-, 184-, and 50-fold selectivity over FGFR1/2/3, respectively.
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eMolecules 32122-11-5 | 4-Benzyloxybenzoic acid methyl ester | Chem-Impex | MFCD00017613 | 242.274 | C15H14O3 | 99.000 | COC(=O)c1ccc(OCc2ccccc2)cc1 | 1g | 386901331
4-Benzyloxybenzoic acid methyl ester | Chem-Impex | 32122-11-5 | MFCD00017613 | 242.274 | C15H14O3 | 99.000 | COC(=O)c1ccc(OCc2ccccc2)cc1 | 1g | 386901331
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Medchemexpress LLC HY-13447A 5mg Medchemexpress, PF429242 (dihydrochloride) CAS:2248666-66-0 Purity:>98%
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Medchemexpress, HY-13447A 5mg PF429242 (dihydrochloride) CAS:2248666-66-0 PF429242 dihydrochloride is a reversible and competitive SREBP site 1 protease (S1P) inhibitor with an IC50 of 175 nM. 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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Medchemexpress LLC HY-10929 5mg Medchemexpress, UNC0224 CAS:1197196-48-7 Purity:>98%
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Medchemexpress, HY-10929 5mg UNC0224 CAS:1197196-48-7 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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Medchemexpress LLC Zm223 hydrochloride | 2438679-27-5 | 98.9% | 538.99 g·mol⁻¹ | C23H18ClF3N4O2S2 | 50 MG
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ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of the NEDD8-activating enzyme (NAE) with demonstrated anticancer activity in cell-based assays. It inhibits proliferation of HCT-116 and U-2OS cells at low-nanomolar IC50s and alters NEDD8 conjugation, producing decreased NEDD8 levels and accumulation of UBC12.
- Orally active non-covalent NAE inhibitor.
- Potent cellular activity (IC50 ≈ 100-122 nM in reported assays).
- Modulates NEDD8 conjugation pathway, useful for mechanistic studies.
- High purity suitable for preclinical research (≈ 98.9%).
- Solid, white to off-white material with recommended cold storage for stock solutions.
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Medchemexpress LLC HY-13032B 5mg Medchemexpress, Molibresib (besylate) CAS:1895049-20-3 Purity:>98%
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Medchemexpress, HY-13032B 5mg Molibresib (besylate) CAS:1895049-20-3 Molibresib besylate (GSK 525762C; I-BET 762 besylate) is a BET bromodomain inhibitor with IC 50 of 32.5-42.5 nM. 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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eMolecules 1188296-52-7 | Medchem Express | PF-4800567 | 5mg | 437899366 | HY-12470 | MFCD22123245 | 359.81 | C17H18ClN5O2
Medchem Express | Petesicatib | 5mg | 475641480 | HY-109069 | 1252637-35-6 | 603.540 | C25H23F6N5O4S
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Medchemexpress LLC 10-methyl-9-(phenoxycarbonyl)acridinium (fluorosulfonate) | 149300-54-9 | MFCD01320487 | 99.8% | 413.42 | C21H16FNO5S | 10 MG
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10-Methyl-9-(phenoxycarbonyl)acridinium (fluorosulfonate) is an acridinium ester reagent that produces chemiluminescence under neutral conditions and is used for measurement of hydrogen peroxide. Supplied as a light-yellow solid for research use; solutions are unstable and should be prepared fresh.
- Chemiluminescent probe for hydrogen peroxide detection.
- Phenyl ester acridinium structure for sensitive signal generation.
- High purity suitable for analytical and research applications.
- Light yellow solid for convenient solid-state handling.
- Unstable in solution; prepare fresh solutions before use.
- Recommended storage sealed at 4°C, protected from moisture and light.
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Medchemexpress LLC Ly367385 hydrochloride | 2829282-00-8 | 99.4% | 245.66 | C10H12ClNO4 | 100 MG
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LY367385 hydrochloride is a selective and potent antagonist of the metabotropic glutamate receptor mGluR1a used in research to investigate mGluR1-mediated signaling, neuroprotective mechanisms, and seizure models. The compound is supplied as a solid suitable for laboratory handling and storage.
- Selective mGluR1a antagonist for receptor-specific studies.
- High reported purity supports reproducible results.
- Solid, stable form suitable for standard laboratory storage.
- Applicable to neuroprotection, anticonvulsant, and antiepileptic research.
- Compatible with common solvent storage conditions for short- and long-term use.
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