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Filtered Search Results
eMolecules 847949-49-9 | Medchem Express | O-Desmethyl gefitinib | 5mg | 784543527 | HY-100064 | MFCD09952182 | 432.88 | C21H22ClFN4O3
Medchem Express | O-Desmethyl gefitinib | 5mg | 784543527 | HY-100064 | 847949-49-9 | MFCD09952182 | 432.880 | C21H22ClFN4O3
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STA Pharmaceutical 1-Fmoc-4-(4-fluorophenyl)-4-carboxypiperidine | 100 g | CAS 1076197-06-2 | MDL MFCD11226817
1-Fmoc-4-(4-fluorophenyl)-4-carboxypiperidine is a Amino Acid reagent (Subcategory: Unusual AA) sold by WuXi TIDES. Offered in 100 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1076197-06-2
- MDL: MFCD11226817
- InChIKey: DPGFVVPTWGNEHH-UHFFFAOYSA-N
- Molecular Weight: 445.49
- Molecular Formula: C27H24FNO4
- Purity: ≥95%
- Container Type: 500 mL HDPE
- Pack Size: 100 g
- Net Weight: 100 g
- Gross Weight: 160.5 g
- Commodity Code: 29333999
- Country Of Origin: China
- IUPAC: 1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-(4-fluorophenyl)piperidine-4-carboxylic acid
- SMILES: O=C(N1CCC(C2=CC=C(C=C2)F)(CC1)C(O)=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
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eMolecules 2248003-71-4 | Medchem Express | AZD3229 Tosylate | 5mg | 441681894 | HY-112802A | 651.71 | C31H34FN7O6S
ChemScene | Methyl 5-(3-nitrophenyl)isoxazole-3-carboxylate | 1g | 632284645 | CS-0150739 | 517870-18-7 | MFCD03778971 | 248.194 | C11H8N2O5
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eMolecules 2829263-20-7 | Medchem Express | FPR2 agonist 2 | 5mg | 791206393 | HY-144604 | 446.458 | C25H20F2N4O2
ChemScene | Di(thiophen-2-yl)methanone | 1g | 536788957 | CS-0043136 | 704-38-1 | MFCD00052096 | 194.270 | C9H6OS2
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Accela Chembio Inc 2-(4-fluorophenyl)ethanol | 25g | 7589-27-7 | MFCD00002898 | 97+% | D: 1.121 | Shelf Life: 1260 Days | Regular
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2-(4-fluorophenyl)ethanol | 25g | 7589-27-7 | MFCD00002898 | 97+% | D: 1.121 | Shelf Life: 1260 Days | Regular
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Medchemexpress LLC HY-18082 100mg , AGI-5198 IDH-C35 CAS:1355326-35-0 Purity:98%
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Medchemexpress, HY-18082 100mg AGI-5198 IDH-C35 CAS:1355326-35-0 Formula:C27H31FN4O2 Purity:98% AGI-5198 is a novel R132H-IDH1 inhibitor, used for cancer treatment. 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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Chemscene ChemScene | 1,2-Dibromo-3,5-difluorobenzene | 100G | CS-0147255 | 0.98 | 139215-43-3| MFCD00042559 | 271.89
ChemScene | 1,2-Dibromo-3,5-difluorobenzene | 100G | CS-0147255 | 0.98 | 139215-43-3| MFCD00042559 | 271.89
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Medchemexpress LLC HY-N0823 5mg Medchemexpress, Lithospermic acid CAS:28831-65-4 Purity:>98%
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Medchemexpress, HY-N0823 5mg Lithospermic acid CAS:28831-65-4 Lithospermic acid ((+)-Lithospermic acid) is a plant-derived polycyclic phenolic carboxylic acid isolated from Salvia miltiorrhiza, and has the anti-oxidative and hepatoprotective activity on carbon tetrachloride (CCl4)-induced acute liver damage in vitro and in vivo. 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 Vorapaxar sulfate | 705260-08-8 | MFCD16038877 | 99.8% | 590.66 g·mol⁻1 | C29H35FN2O8S | 10 MG
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Vorapaxar sulfate is the sulfate salt form of vorapaxar, a selective protease-activated receptor-1 (PAR-1) antagonist used in research to study antiplatelet mechanisms. Supplied as a research reagent (commonly as a 10 mg solid vial), it is provided with documented chemical identifiers and high purity suitable for analytical and preclinical work.
- Selective PAR-1 antagonist that inhibits platelet aggregation.
- Sulfate salt form enhances stability and handling for assays.
- High purity suitable for analytical and preclinical research.
- Well characterized with CAS and database identifiers for traceability.
- Molecular weight and formula available for formulation and dosing calculations.
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Medchemexpress LLC HY-13449 5mg Medchemexpress, TAK-733 CAS:1035555-63-5 Purity:>98%
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Medchemexpress, HY-13449 5mg TAK-733 CAS:1035555-63-5 TAK-733 is a potent and selective MEK allosteric site inhibitor with an IC50 of 3.2 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 (Rac)-lunresertib | 2719749-28-5 | MFCD34645920 | 99.7% | C18H20N4O2 | 10MG
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Lunresertib (racemic) is an orally bioavailable small-molecule inhibitor of PKMYT1 (Myt1) used in preclinical research to study cell-cycle regulation and anticancer activity. It exhibits potent kinase inhibition and is supplied at high analytical purity for laboratory experiments.
- Potent PKMYT1 inhibitor with IC50 <10 nM.
- Orally bioavailable small-molecule suitable for cellular and biochemical studies.
- High analytical purity (about 99.7%).
- Molecular formula C18H20N4O2 and molecular weight 324.38 g/mol.
- Supplied in small research pack sizes for laboratory use.
- Useful for cell-cycle and anticancer mechanism studies.
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eMolecules 156682-52-9 | Ambeed | 14-Dibromo-23-difluorobenzene | 1g | 524993336 | A105757 | MFCD09835192 | 271.887 | C6H2Br2F2
AstaTech | (1-BROMO-3-CHLOROPROPYL)BENZENE | 1g | 449751984 | AB10338 | 95.000 | 21763-00-8 | MFCD18206038 | 233.530 | C9H10BrCl
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B/VIRGINIA/ATCC5/2012
B/VIRGINIA/ATCC5/2012
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Medchemexpress LLC HY-18018 5mg Medchemexpress, RN486 CAS:1242156-23-5 Purity:>98%
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Medchemexpress, HY-18018 5mg RN486 CAS:1242156-23-5 RN486 is a potent, selective and orally active Btk inhibitor with an IC50 of 4.0 nM and a Kd of 0.31 nM. RN486 is less active for other kinases. RN486 can be used for rheumatoid arthritis and systemic lupus erythematosus research. 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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Selleck Chemical LLC JNJ 31020028
JNJ 31020028 is a novel neuropeptide Y Y2 receptor antagonist which bound with high affinity with human and rat Y2 receptor (pIC50 8 07 0 05 for human Y2 receptor and pIC50 8 22 0 06 for rat Y2 receptor) and 100-fold selective versus human Y1 Y4 and Y5 receptors
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