"MEDCHEMEXPRESS"
MS21 AKT degrader 1mg 1 * 1 mg
Supplier: MEDCHEMEXPRESS
MS21 AKT degrader 1mg 1 * 1 mg
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N8-ACETYLSPERMIDINE DIHYDROCHLORIDE 1 * 5 mg
Supplier: MEDCHEMEXPRESS
N8-ACETYLSPERMIDINE DIHYDROCHLORIDE 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: SOLUBLE TO 100 MM IN DMSO
TCS JNK 5A(JNK INHIBITOR IX) IS A SELECTIVE INHIBITOR OF JNK2 AND JNK3 (PIC50 VALUES ARE 6.7, 6.5, <5.0 AND <4.8 FOR JNK3, JNK2, JNK1 AND P38Α RESPECTIVELY) DISPLAYS NO SI 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: SOLUBLE TO 100 MM IN DMSO
TCS JNK 5A(JNK INHIBITOR IX) IS A SELECTIVE INHIBITOR OF JNK2 AND JNK3 (PIC50 VALUES ARE 6.7, 6.5, <5.0 AND <4.8 FOR JNK3, JNK2, JNK1 AND P38Α RESPECTIVELY) DISPLAYS NO SI 1 * 10 mg
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Chloroquine - 100 mg 1 * 100 mg
Supplier: MEDCHEMEXPRESS
Chloroquine - 100 mg 1 * 100 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 50 MG/ML
CAPSAZEPINE IS A SYNTHETIC ANALOGUE OF THE SENSORY NEURONE EXCITOT OXIN, CAPSAICIN POTENT TRPV1 RECEPTOR ANTAGONIST WITH IC50 OF 562 NM. IC50 VALUE: 562 NM (RAT TRPV1) [1]CAPSAZEPINE 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 50 MG/ML
CAPSAZEPINE IS A SYNTHETIC ANALOGUE OF THE SENSORY NEURONE EXCITOT OXIN, CAPSAICIN POTENT TRPV1 RECEPTOR ANTAGONIST WITH IC50 OF 562 NM. IC50 VALUE: 562 NM (RAT TRPV1) [1]CAPSAZEPINE 1 * 50 mg
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BAVDEGALUTAMIDE (98%) 1 * 2 g
Supplier: MEDCHEMEXPRESS
BAVDEGALUTAMIDE (98%) 1 * 2 g
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HER2/CD340 Protein, Human (630a.a, HEK293, His) 1 * 50 µG
Supplier: MEDCHEMEXPRESS
HER2/CD340 Protein, Human (630a.a, HEK293, His) 1 * 50 µG
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
BAY 87-2243 IS A HIGHLY POTENT AND SELECTIVE INHIBITOR OF HYPOXIA- INDUCED HIF-1 ACTIVATION.IC50 VALUE: 2.0 NM(CA9 IN HCT116LUC CELLS) [1]TARGET: HIF-1IN VITRO: BAY 87-2243 INHIBITED L 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
BAY 87-2243 IS A HIGHLY POTENT AND SELECTIVE INHIBITOR OF HYPOXIA- INDUCED HIF-1 ACTIVATION.IC50 VALUE: 2.0 NM(CA9 IN HCT116LUC CELLS) [1]TARGET: HIF-1IN VITRO: BAY 87-2243 INHIBITED L 1 * 10 mg
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SOLUBILITY: DMSO: ≥ 36 MG/ML
RUXOLITINIB(INCB018424) IS THE FIRST POTENT, SELECTIVE, JAK1/2 INHIBITOR TO ENTER THE CLINIC WITH IC 50 OF 3.3 NM/2.8 NM, >130-FOLD SELECTIVITY FOR JAK1/2 VERSUS JAK3. IC50 VALUE: 3.3 NM/2.8 NM(JAK1/JAK2)TARGET: JAK1/2 1 * 5 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: DMSO: ≥ 36 MG/ML
RUXOLITINIB(INCB018424) IS THE FIRST POTENT, SELECTIVE, JAK1/2 INHIBITOR TO ENTER THE CLINIC WITH IC 50 OF 3.3 NM/2.8 NM, >130-FOLD SELECTIVITY FOR JAK1/2 VERSUS JAK3. IC50 VALUE: 3.3 NM/2.8 NM(JAK1/JAK2)TARGET: JAK1/2 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 20 MG/ML, H2O: ＜ 1 MG/ML
PD0325901 (PD325901) IS SELECTIVE AND NON ATP-C OMPETITIVE MEK INHIBITOR WITH IC50 OF 0.33 NM.IC50 VALUE:TARGET: MEKPD0325901 IS A SELECTIVE MEK1 AND MEK2 INHIBITOR. 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 20 MG/ML, H2O: ＜ 1 MG/ML
PD0325901 (PD325901) IS SELECTIVE AND NON ATP-C OMPETITIVE MEK INHIBITOR WITH IC50 OF 0.33 NM.IC50 VALUE:TARGET: MEKPD0325901 IS A SELECTIVE MEK1 AND MEK2 INHIBITOR. 1 * 10 mg
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5-fluoro-N-{2-[(2S)-1-methyl-2-pyrrolidi 1 * 5 mg
Supplier: MEDCHEMEXPRESS
5-fluoro-N-{2-[(2S)-1-methyl-2-pyrrolidi 1 * 5 mg