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Filtered Search Results
eMolecules 850583-75-4 | 3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione | Combi-Blocks, Inc. | MFCD20257907 | 300.350 | C14H8N2O2S2 | 98.000 | O=C1NC(=C2C(=O)NC(=C12)c1cccs1)c1cccs1 | 25g | 569293009
3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione | Combi-Blocks, Inc. | 850583-75-4 | MFCD20257907 | 300.350 | C14H8N2O2S2 | 98.000 | O=C1NC(=C2C(=O)NC(=C12)c1cccs1)c1cccs1 | 25g | 569293009
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eMolecules 365215-38-9 | (R,R)-Bn-Pybox | ChemScene | MFCD23704922 | 397.478 | C25H23N3O2 | 95.000 | C([C@@H]1COC(=N1)c1cccc(n1)C1=N[C@H](Cc2ccccc2)CO1)c1ccccc1 | 1g | 536799837
(R,R)-Bn-Pybox | ChemScene | 365215-38-9 | MFCD23704922 | 397.478 | C25H23N3O2 | 95.000 | C([C@@H]1COC(=N1)c1cccc(n1)C1=N[C@H](Cc2ccccc2)CO1)c1ccccc1 | 1g | 536799837
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Medchemexpress LLC Prexasertib dihydrochloride | 1234015-54-3 | MFCD25977016 | 99.7% | 10 MG
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Prexasertib dihydrochloride is a selective, ATP-competitive CHK1 inhibitor used in preclinical research to probe checkpoint signaling, replication stress, and DNA damage-induced apoptosis. It is suitable for biochemical and cellular assays investigating antitumor mechanisms and pathway dependencies.
- High potency against CHK1 (Ki 0.9 nM; IC50 <1 nM).
- Also inhibits CHK2 and RSK1 at low nanomolar concentrations (CHK2 IC50 8 nM; RSK1 IC50 9 nM).
- Available as solid powder and as DMSO solutions for flexible assay formats.
- Reported high purity appropriate for preclinical studies.
- Useful for studies of DNA damage response, replication catastrophe, and apoptosis.
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Selleck Chemical LLC Iptacopan Hydrochloride
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Iptacopan Hydrochloride is a first-in-class orally administered potent and highly selective factor B inhibitor with an IC50 of 12 nM and a Kd value of 7 9 nM Iptacopan exhibits excellent selectivity over other proteases affording IC50s of 30 M across a panel of 41 human proteases
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Aobchem AOBCHEM
5001076560 -BROMO-2-CHLORO-4- MORPHOLIN-
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Aobchem AOBCHEM
5001076628 -BROMO-2-CHLORO-4- MORPHOLIN-
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TARGETMOL CHEMICALS INC EPIRUBICIN HYDROCHLORIDE 25MG
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Epirubicin hydrochloride (Pharmorubicin) is an antineoplastic agent which can inhibit Topoisomerase. purity: 99%
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TARGETMOL CHEMICALS INC MB-07729 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. MB-07729 is a potent non-competitive inhibitor of fructose-16-bisphosphate with IC50 values of 189 121 and 31 nM in rat monkey and human respectively for the study of diabetes. purity: 99%
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TARGETMOL CHEMICALS INC ACHP HYDROCHLORIDE 5MG
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502694212 ACHP HYDROCHLORIDE 5MG
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eMolecules Aladdin Scientific Corporation (2-Dicyclohexylphosphino-2?6?-diisopropoxy-11?-biphenyl)[2-(2?-amino-11?-biphenyl)]palladium(II) methanesulfonate 25g 845266592 M396600 1445085-77-7 [null] 838.390 C43H58NO5PPdS
Aladdin Scientific Corporation (2-Dicyclohexylphosphino-2?6?-diisopropoxy-11?-biphenyl)[2-(2?-amino-11?-biphenyl)]palladium(II) methanesulfonate 25g 845266592 M396600 1445085-77-7 [null] 838.390 C43H58NO5PPdS
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Selleck Chemical LLC Mebeverine Hydrochloride S5027-25mg
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Mebeverine (Duspatalin Duspatal Colofac) a 3-phenylethylamine derivative of methoxybenzamine acts as a musculotropic antispasmodic agent
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Selleck Chemical LLC Irinotecan hydrochloride S5026-1g
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Irinotecan (CPT-11 ( )-Irinotecan) hydrochloride is an inhibitor of Topoisomerase I (Topo I) that exhibits cytotoxicity in LoVo cells and HT-29 cells with IC50 of 15 8 M and 5 17 M respectively
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Selleck Chemical LLC Fendiline hydrochloride S5279-25mg
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Fendiline hydrochloride is the hydrochloride salt form of Fendiline which is an L-type calcium channel blocker and also a specific inhibitor of K-Ras plasma membrane targeting with no detectable effect on the localization of H- and N-Ras
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Selleck Chemical LLC Trihexyphenidyl hydrochloride S4542-100mg
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Trihexyphenidyl hydrochloride (Benzhexol Artane) is an antiparkinsonian agent of the antimuscarinic class
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Selleck Chemical LLC Dasatinib hydrochloride S5254-10mM/1mL
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Dasatinib hydrochloride (BMS-354825) is the hydrochloride salt form of dasatinib an inhibitor that targets Abl Src and c-Kit with IC50 of 1 nM 0 8 nM and 79 nM in cell-free assays respectively
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