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Filtered Search Results
Medchemexpress LLC HY-N0336 5mg Medchemexpress, 3-Butylidenephthalide CAS:551-08-6 Purity:>98%
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Medchemexpress, HY-N0336 5mg 3-Butylidenephthalide CAS:551-08-6 3-Butylidenephthalide (Butylidenephthalide) is a phthalic anhydride derivative identified in Ligusticum chuanxiong Hort, and has larvicidal activity (LC50 of 1.56 mg/g for Spodoptera litura larvae). 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-100779 100mg Medchemexpress, Rimacalib CAS:215174-50-8 Purity:>98%
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Medchemexpress, HY-100779 100mg Rimacalib CAS:215174-50-8 Rimacalib is a Ca 2+ /calmodulin-dependent protein kinase II (CaMKII) inhibitor, with IC 50 s of ~1 μM for CaMKIIα to ~30 μM for CaMKIIγ. 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 4-chloro-2-fluorobenzoic acid | 446-30-0 | MFCD00042468 | 99.3% | 174.56 | C7H4ClFO2 | 50 G
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4-Chloro-2-fluorobenzoic acid is a halogenated benzoic acid used as a biochemical reagent and building block in organic and medicinal chemistry. It is supplied as a solid with high purity and is intended for research applications such as synthesis, assay development, and structure-activity investigations.
- High purity for reliable experimental results.
- Suitable as an intermediate for organic synthesis.
- Applicable in medicinal chemistry and SAR studies.
- Available in multiple pack sizes for lab-scale use.
- Characterization data (HNMR, RP-HPLC) and safety documents available.
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Medchemexpress LLC Golgicide A | 1139889-93-2 | MFCD27937048 | >98.0% | 284.30 g/mol | C17H14F2N2 | 50 MG
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Golgicide A is a small-molecule, reversible inhibitor of the cis-Golgi ADP-ribosylation factor guanine nucleotide exchange factor GBF1, used as a research reagent to probe Golgi function and viral replication. It is intended for laboratory research use only.
- Potent, highly specific, reversible inhibitor of GBF1.
- Reduces replication of coxsackievirus B3 and other enteroviruses.
- Useful for studying Golgi trafficking, membrane dynamics, and virus-host interactions.
- Typical purity ≥98% suitable for biochemical and cell-based assays.
- Molecular weight 284.30 g/mol; formula C17H14F2N2; CAS 1139889-93-2.
- Supplied in formats appropriate for laboratory use; research use only.
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Medchemexpress LLC HY-19712 5mg Medchemexpress, LJH685 CAS:1627710-50-2 Purity:>98%
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Medchemexpress, HY-19712 5mg LJH685 CAS:1627710-50-2 LJH685 is a potent, specific and selective RSK inhibitor, inhibits RSK1, 2, and 3 biochemical activities with IC50s of 6, 5, 4 nM, respectively. 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 Op-5244 sodium | 00-00-0 | 99.9% | C19H28ClN5NaO9P | 10MG
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OP-5244 sodium is the sodium salt of a potent, orally active small-molecule CD73 inhibitor that reverses immunosuppression by blocking adenosine production. Supplied for research use as a characterized solid with accompanying purity and analytical data.
- Potent CD73 inhibitor (IC50 0.25 nM).
- Reverses adenosine-mediated immunosuppression.
- High purity (99.9%).
- Chemical formula C19H28ClN5NaO9P; molecular weight 559.87 g·mol⁻¹.
- Available in small research quantities such as 10 mg.
- Solid form; store sealed at 4 °C.
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Medchemexpress LLC Aurora kinase inhibitor II | 331770-21-9 | 99.1% | 400.43 g·mol⁻1 | C23H20N4O3 | 5 MG
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Aurora kinase inhibitor-2 is a selective, ATP-competitive small-molecule inhibitor of Aurora kinases A and B used in biochemical and cell-based research. It shows inhibitory activity in the low hundreds of nanomolar range and is supplied as a solid suitable for in vitro and in vivo formulation studies.
- Selective ATP-competitive inhibitor of Aurora A and Aurora B (IC50: Aurora A 310 nM; Aurora B 240 nM).
- Supplied as a white to yellow solid with high reported purity (~99.1%).
- Molecular formula C23H20N4O3 and molecular weight 400.43 g·mol⁻1.
- Dissolves readily in DMSO; recommended in vitro solubility 100 mg/mL (ultrasonic may be required).
- Formulatable for in vivo studies using common vehicles (SBE-β-CD, corn oil, PEG300/Tween-80 mixes).
- Intended for research applications probing Aurora kinase function and signaling.
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STA Pharmaceutical 1-Fmoc-4-(4-fluorophenyl)-4-carboxypiperidine | 5 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 5 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: 30 mL HDPE
- Pack Size: 5 g
- Net Weight: 5 g
- Gross Weight: 16.5 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 190011-84-8 | Ambeed | 2-Amino-46-difluorobenzonitrile | 1g | 665578916 | A424613 | MFCD13178245 | 154.12 | C7H4F2N2
Medchem Express | Thrombin Inhibitor 2 | 5mg | 779532904 | HY-10217 | 312904-62-4 | 452.820 | C19H16ClF3N6O2
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eMolecules 1038984-31-4 | Medchem Express | Tulrampator | 5mg | 441681806 | HY-109046 | 380.379 | C20H17FN4O3
Medchem Express | SM-433 | 5mg | 686240464 | HY-138059 | 1071992-81-8 | 561.727 | C32H43N5O4
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eMolecules 1430213-30-1 | Medchem Express | ML216 | 5mg | 446261081 | HY-12342 | MFCD24849400 | 383.32 | C15H9F4N5OS
Medchem Express | GNE-375 | 5mg | 721434650 | HY-123621 | 1926989-06-1 | 451.523 | C25H29N3O5
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eMolecules 4-Bromo-2,5-difluorobenzenesulfonamide | 214209-98-0 | MFCD01569463 | 1g
Matrix Scientific | 4-Bromo-2,5-difluorobenzenesulfonamide | 1g | 389712425 | 1283 | | 214209-98-0 | MFCD01569463 | 272.060 | C6H4BrF2NO2S
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Medchemexpress LLC Abemaciclib metabolite M2 | 1231930-57-6 | 99.8% | 10 MG
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Abemaciclib metabolite M2 is a potent CDK4 and CDK6 inhibitor, acting as a metabolite of Abemaciclib. It exhibits anti-cancer activity with IC50s of 1.2 nM for CDK4 and 1.3 nM for CDK6. This metabolite is the most prominent and active plasma metabolite found in humans. It shows plasma protein binding in rat, dog, and human between 83-92%.
- Acts as a potent CDK4 and CDK6 inhibitor
- Exhibits anti-cancer activity
- Most prominent and active plasma metabolite in humans
- Shows plasma protein binding in rat, dog, and human (83-92%)
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eMolecules 743420-02-2 | N-(2-Amino-5-fluorophenyl)-4-((3-(pyridin-3-yl)acrylamido)methyl)benzamide | MFCD18382123 | 10mg
Ambeed | N-(2-Amino-5-fluorophenyl)-4-((3-(pyridin-3-yl)acrylamido)methyl)benzamide | 10mg | 534576096 | A186722 | 743420-02-2 | MFCD18382123 | 390.418 | C22H19FN4O2
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eMolecules 882290-02-0 | N'-(3-Chloro-4-fluorophenyl)-2-(4-chlorophenyl)-2-oxoacetohydrazonoyl cyanide | 10mg
Ambeed | N'-(3-Chloro-4-fluorophenyl)-2-(4-chlorophenyl)-2-oxoacetohydrazonoyl cyanide | 10mg | 598441919 | A1359457 | 882290-02-0 | 336.150 | C15H8Cl2FN3O
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