"MEDCHEMEXPRESS"
PF-04979064_1220699-06-8_HY-100398__25_M 1 * 25 mg
Supplier: MEDCHEMEXPRESS
PF-04979064_1220699-06-8_HY-100398__25_M 1 * 25 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
TRAMETINIB (GSK1120212 JTP 74057) IS A HIGHLY SPECIFIC AND POTENT MEK1/2 INHIBITOR WITH IC50 OF 0.92 NM/1.8 NM, NO INHIBITION OF THE KINASE ACTIVITIES OF C-RAF, B-RAF, ERK1/2.IC50 VA 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
TRAMETINIB (GSK1120212 JTP 74057) IS A HIGHLY SPECIFIC AND POTENT MEK1/2 INHIBITOR WITH IC50 OF 0.92 NM/1.8 NM, NO INHIBITION OF THE KINASE ACTIVITIES OF C-RAF, B-RAF, ERK1/2.IC50 VA 1 * 50 mg
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SOLUBILITY: DMSO ≥ 26 MG/ML
FCCP IS AN UNCOUPLER OF OXIDATIVE PHOSPHORYLATION IN MITOCHONDRIA. 1 * 10 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: DMSO ≥ 26 MG/ML
FCCP IS AN UNCOUPLER OF OXIDATIVE PHOSPHORYLATION IN MITOCHONDRIA. 1 * 10 mg
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Dabigatran etexilate 1 * 100 mg
Supplier: MEDCHEMEXPRESS
Dabigatran etexilate 1 * 100 mg
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Dabigatran etexilate mesilate 50 mg bottle 1 * 50 mg
Supplier: MEDCHEMEXPRESS
Dabigatran etexilate mesilate 50 mg bottle 1 * 50 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:35MG/ML
AS601245 IS AN INHIBITOR OF THE C-JUN NH2-TERMINAL KINASE (JNK) (HJ NK1: IC50=150NM, HJNK2: IC50=220NM AND HJNK3: IC50=70 NM), HAS NEUROPROTECTIVE PROPERTIES.IC50 VALUE: 150NM (HJNK1), 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:35MG/ML
AS601245 IS AN INHIBITOR OF THE C-JUN NH2-TERMINAL KINASE (JNK) (HJ NK1: IC50=150NM, HJNK2: IC50=220NM AND HJNK3: IC50=70 NM), HAS NEUROPROTECTIVE PROPERTIES.IC50 VALUE: 150NM (HJNK1), 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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MK-3207 HYDROCHLORIDE 1 * 100 mg
Supplier: MEDCHEMEXPRESS
MK-3207 HYDROCHLORIDE 1 * 100 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥190MG/ML WATER <1.2MG/ML ETHANOL <1.2MG/ML
ABT-263 (NAVITOCLAX) IS A POTEN T INHIBITOR OF BCL-XL, BCL-2 AND BCL-W WITH KI OF ≤ 0.5 NM, ≤1 NM AND ≤1 NM.IC50 VALUE: ≤ 0.5 NM(KI FOR BCL-XL) ≤1 N 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥190MG/ML WATER <1.2MG/ML ETHANOL <1.2MG/ML
ABT-263 (NAVITOCLAX) IS A POTEN T INHIBITOR OF BCL-XL, BCL-2 AND BCL-W WITH KI OF ≤ 0.5 NM, ≤1 NM AND ≤1 NM.IC50 VALUE: ≤ 0.5 NM(KI FOR BCL-XL) ≤1 N 1 * 10 mg
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SOLUBILITY: H2O (100 MM) OR PBS (100 MM)
Y-27632 IS A SELECTIVE ROCK1 (P160ROCK) INHIBITOR WITH KI OF 140 NM, EXHIBITS >200-FOLD SELECTIVITY OVER OTHER KINASES, INCLUDING PKC, CAMP-DEPENDENT PROTEIN KINASE, MLCK AND PAK.IC50 VALUE: 140 NM (KI)TARG 1 * 5 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: H2O (100 MM) OR PBS (100 MM)
Y-27632 IS A SELECTIVE ROCK1 (P160ROCK) INHIBITOR WITH KI OF 140 NM, EXHIBITS >200-FOLD SELECTIVITY OVER OTHER KINASES, INCLUDING PKC, CAMP-DEPENDENT PROTEIN KINASE, MLCK AND PAK.IC50 VALUE: 140 NM (KI)TARG 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 100 MM IN DMSO；
FR180204 IS A POTENT AND SELECTIVE ATP-COMPETITIVE INHIBITOR OF ERK1 AND ERK2 WITH KI VALUE OF 0.31 UM AND 0.14 UM RESPECTIVELY HAS IC50 VALUES OF 0.51 AND 0.33 ΜM IN ENZYMATIC ASSA 1 * 1 mL
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 100 MM IN DMSO；
FR180204 IS A POTENT AND SELECTIVE ATP-COMPETITIVE INHIBITOR OF ERK1 AND ERK2 WITH KI VALUE OF 0.31 UM AND 0.14 UM RESPECTIVELY HAS IC50 VALUES OF 0.51 AND 0.33 ΜM IN ENZYMATIC ASSA 1 * 1 mL
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Catalogus #: 83639.320
Leverancier: VWR Chemicals
Catalogus #: 20864.320
Leverancier: VWR Chemicals
Catalogus #: 215-1592
Leverancier: VWR Collection
Catalogus #: 83640.320
Leverancier: VWR Chemicals
Catalogus #: 31770.294
Leverancier: VWR Chemicals
Catalogus #: 1.00030.2500
Leverancier: Merck
Catalogus #: 83645.320
Leverancier: VWR Chemicals
Catalogus #: 20060.320
Leverancier: VWR Chemicals