1243 Results for: "MEDCHEMEXPRESS"
Belotecan-d7 hydrochloride - 1 m
Supplier: MEDCHEMEXPRESS
Belotecan-d7 hydrochloride - 1 m
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Cagrilintide acetate is a non-selective AMYR/CTR agonist and long-acting acylated amylase analogue. Cagrilintide acetate causes a re duction in food intake and significant weight loss in a dose-dependent manner. Cagrilintide acetate can be used in ob 1 * 10 mg
Supplier: MEDCHEMEXPRESS
Cagrilintide acetate is a non-selective AMYR/CTR agonist and long-acting acylated amylase analogue. Cagrilintide acetate causes a re duction in food intake and significant weight loss in a dose-dependent manner. Cagrilintide acetate can be used in ob 1 * 10 mg
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E-7386 CBP/BETA-CATENIN MODULATOR 1 * 10 mg
Supplier: MEDCHEMEXPRESS
E-7386 CBP/BETA-CATENIN MODULATOR 1 * 10 mg
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Blinatumomab (Anatumomab) is a bispecific monoclonal antibody with two binding sites, one for CD3E on T cells and one for CD19 on B cells. Blinatumomab can be used in research for acute lymphoblastic leukemia[1][2][3][4]. 1 * 100 µG
Supplier: MEDCHEMEXPRESS
Blinatumomab (Anatumomab) is a bispecific monoclonal antibody with two binding sites, one for CD3E on T cells and one for CD19 on B cells. Blinatumomab can be used in research for acute lymphoblastic leukemia[1][2][3][4]. 1 * 100 µG
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥22MG/ML WATER <1.2MG/ML ETHANOL ≥122MG/ML
VOLASERTIB(BI6727) IS A HIGHLY P OTENT PLK1 INHIBITOR WITH AN IC50 OF 0.87 NM SHOWS 6- AND 65-FOLD GREATER SELECTIVITY AGAINST PLK2 AND PLK3.IC50 VAL 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥22MG/ML WATER <1.2MG/ML ETHANOL ≥122MG/ML
VOLASERTIB(BI6727) IS A HIGHLY P OTENT PLK1 INHIBITOR WITH AN IC50 OF 0.87 NM SHOWS 6- AND 65-FOLD GREATER SELECTIVITY AGAINST PLK2 AND PLK3.IC50 VAL 1 * 5 mg
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Tivantinib (Synonyms: ARQ 197) 1 * 5 mg
Supplier: MEDCHEMEXPRESS
Tivantinib (Synonyms: ARQ 197) 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: SOLUBLE TO 75 MM IN DMSO AND TO 5 MM IN ETHANOL
GW843682X IS A SELECTIVE PLK1 AN D PLK3 INHIBITOR WITH IC50S OF 2.2 NM(PLK1) AND 9.1 NM(PLK3) DISPLAYS > 100-FOLD SELECTIVITY OVER ~30 OTHER KINASES 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: SOLUBLE TO 75 MM IN DMSO AND TO 5 MM IN ETHANOL
GW843682X IS A SELECTIVE PLK1 AN D PLK3 INHIBITOR WITH IC50S OF 2.2 NM(PLK1) AND 9.1 NM(PLK3) DISPLAYS > 100-FOLD SELECTIVITY OVER ~30 OTHER KINASES 1 * 5 mg
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WYE-132 [1144068-46-1] 1 * 10 mg
Supplier: MEDCHEMEXPRESS
WYE-132 [1144068-46-1] 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:39MG/ML
THZ2 IS A POTENT AND SELECTIVE CDK7 INHIBITOR WITH IN VITRO IC50 OF 13.9 NM.IC50 VALUE: 13.9 NMTARGET: CDK7 INHIBITORMORE INFORMATION CAN BE FOUND IN THE FOLLOWING PATENT: (I-18)PREPAR 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:39MG/ML
THZ2 IS A POTENT AND SELECTIVE CDK7 INHIBITOR WITH IN VITRO IC50 OF 13.9 NM.IC50 VALUE: 13.9 NMTARGET: CDK7 INHIBITORMORE INFORMATION CAN BE FOUND IN THE FOLLOWING PATENT: (I-18)PREPAR 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:25MG/ML
L-778123 HYDROCHLORIDE IS AN INHIBITOR OF FPTASE AND GGPTASE-I WITH IC50 OF 2 NM AND 98 NM IN ENZYME INHIBITION DETERMINATION.IC50 VALUE: 2 NM [1]TARGET: FPTASEIN VITRO: L-778123 CAN C 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:25MG/ML
L-778123 HYDROCHLORIDE IS AN INHIBITOR OF FPTASE AND GGPTASE-I WITH IC50 OF 2 NM AND 98 NM IN ENZYME INHIBITION DETERMINATION.IC50 VALUE: 2 NM [1]TARGET: FPTASEIN VITRO: L-778123 CAN C 1 * 10 mg
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KU-60019 [925701-46-8] 1 * 10 mg
Supplier: MEDCHEMEXPRESS
KU-60019 [925701-46-8] 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 30 MG/ML
RO3280 IS A POTENT, HIGHLY SELECTIVE INHIBITOR OF POLO-LIKE KIN ASE 1 (PLK1) WITH IC50 OF 3 NM.IC50 VALUE: 3 NM (PLK1) [1]TARGET: PLKIN VITRO: DIFLUORO-ANALOG 7 (RO3280) GAVE THE BE 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 30 MG/ML
RO3280 IS A POTENT, HIGHLY SELECTIVE INHIBITOR OF POLO-LIKE KIN ASE 1 (PLK1) WITH IC50 OF 3 NM.IC50 VALUE: 3 NM (PLK1) [1]TARGET: PLKIN VITRO: DIFLUORO-ANALOG 7 (RO3280) GAVE THE BE 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
GILTERITINIB(ASP-2215) IS A POTENT FLT3/AXL INHIBITOR WITH IC50 OF 0.29 NM/<1 NM RESPECTIVELY SHOWS POTENT ANTILEUKEMIC ACTIVITY AGAINST AML WITH EITHER OR BOTH FLT3-ITD AND FLT3-D83 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
GILTERITINIB(ASP-2215) IS A POTENT FLT3/AXL INHIBITOR WITH IC50 OF 0.29 NM/<1 NM RESPECTIVELY SHOWS POTENT ANTILEUKEMIC ACTIVITY AGAINST AML WITH EITHER OR BOTH FLT3-ITD AND FLT3-D83 1 * 50 mg
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HEPARAN SULFATE 1 * 10 mg
Supplier: MEDCHEMEXPRESS
HEPARAN SULFATE 1 * 10 mg
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(Rac)-JBJ-04-125-02 1 * 50 mg
Supplier: MEDCHEMEXPRESS
(Rac)-JBJ-04-125-02 1 * 50 mg
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Neurokin 1 receptor agonist Substance P 5mg 1 * 5 mg
Supplier: MEDCHEMEXPRESS
Neurokin 1 receptor agonist Substance P 5mg 1 * 5 mg
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CART (55-102) 1mg 1 * 1 mg
Supplier: MEDCHEMEXPRESS
CART (55-102) 1mg 1 * 1 mg
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TAK-243 (Synonyms: MLN7243) - 10mg 1 * 10 mg
Supplier: MEDCHEMEXPRESS
TAK-243 (Synonyms: MLN7243) - 10mg 1 * 10 mg
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IMP-1710 is a potent and selective deubiquitylating enzyme UCHL1 inhibitor with an IC50 value of 38 nM. IMP-1710 has antifibrotic ac tivity. IMP-1710 is a UCHL1 probe to identify and quantify target proteins in intact human cells[1]. IMP-1710 is a cl 1 * 1 mg
Supplier: MEDCHEMEXPRESS
IMP-1710 is a potent and selective deubiquitylating enzyme UCHL1 inhibitor with an IC50 value of 38 nM. IMP-1710 has antifibrotic ac tivity. IMP-1710 is a UCHL1 probe to identify and quantify target proteins in intact human cells[1]. IMP-1710 is a cl 1 * 1 mg
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Supplier: KIMBERLY CLARK
Supplier: tempmate
Supplier: Integra
Supplier: Industrial Physics
Supplier: Testo
Supplier: Integra
Supplier: VWR Collection
Supplier: VWR Collection
Supplier: VWR Collection
Supplier: Thermo Fisher Scientific
Supplier: VWR Collection
Supplier: Corning
Supplier: VWR Collection
Supplier: Integra
Supplier: VWR Collection
Supplier: Industrial Physics