"MEDCHEMEXPRESS"
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO >58 MG/ML
BV6 IS A SMALL-MOLECULE SMAC MIMETIC, WHICH ANTAGONIZES IAP AND I NDUCES AUTOUBIQUITINATION AND SUBSEQUENT PROTEASOMAL DEGRADATION OF CIAP1 AND CIAP2.IC50 VALUE:TARGET: IAP ANTAGONIST 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO >58 MG/ML
BV6 IS A SMALL-MOLECULE SMAC MIMETIC, WHICH ANTAGONIZES IAP AND I NDUCES AUTOUBIQUITINATION AND SUBSEQUENT PROTEASOMAL DEGRADATION OF CIAP1 AND CIAP2.IC50 VALUE:TARGET: IAP ANTAGONIST 1 * 5 mg
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LY-2584702 TOSYLATE SALT 10 MM * 1 ML IN DMSO 1 * 1 mL
Supplier: MEDCHEMEXPRESS
LY-2584702 TOSYLATE SALT 10 MM * 1 ML IN DMSO 1 * 1 mL
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HOMO-PROTAC CEREBLON DEGRADER 1 SOLUBILITY: DMSO : 200 MG/ML (302.74 MM NEED ULTRASONIC) 1 * 5 mg
Supplier: MEDCHEMEXPRESS
HOMO-PROTAC CEREBLON DEGRADER 1 SOLUBILITY: DMSO : 200 MG/ML (302.74 MM NEED ULTRASONIC) 1 * 5 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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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥20 MG/ML
S-(+)-CLOPIDOGREL HYDROGEN SULFATE IS THE S ENANTIOMER OF CLOPID OGREL AND A P2Y12 RECEPTOR INHIBITOR. TARGET: P2Y RECEPTORCLOPIDOGREL IS AN EFFECTIVE ANTIPLATELET AGENT USEFUL FOR T 1 * 100 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥20 MG/ML
S-(+)-CLOPIDOGREL HYDROGEN SULFATE IS THE S ENANTIOMER OF CLOPID OGREL AND A P2Y12 RECEPTOR INHIBITOR. TARGET: P2Y RECEPTORCLOPIDOGREL IS AN EFFECTIVE ANTIPLATELET AGENT USEFUL FOR T 1 * 100 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO (FREE SOLUBLE)
IRBINITINIB(ARRY-380 ONT-380) IS A POTENT AND SELE CTIVE HER2 INHIBITOR WITH IC50 OF 8 NM, EQUIPOTENT AGAINST TRUNCATED P95-HER2, 500-FOLD MORE SELECTIVE FOR HER2 VERSU 1 * 100 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO (FREE SOLUBLE)
IRBINITINIB(ARRY-380 ONT-380) IS A POTENT AND SELE CTIVE HER2 INHIBITOR WITH IC50 OF 8 NM, EQUIPOTENT AGAINST TRUNCATED P95-HER2, 500-FOLD MORE SELECTIVE FOR HER2 VERSU 1 * 100 mg
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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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BAVDEGALUTAMIDE (98%) 1 * 2 g
Supplier: MEDCHEMEXPRESS
BAVDEGALUTAMIDE (98%) 1 * 2 g
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24, 25-DIHYDROXY VD2 1 * 25 mg
Supplier: MEDCHEMEXPRESS
24, 25-DIHYDROXY VD2 1 * 25 mg
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GJA1 Protein, Human (His) -- 10µg 1 * 10 µG
Supplier: MEDCHEMEXPRESS
GJA1 Protein, Human (His) -- 10µg 1 * 10 µG
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 4.7 MG/ML
FTI-277 HCL IS AN INHIBITOR OF FARNESYL TRANSFERASE (FTASE) A HIGHLY POTENT RAS CAAX PEPTIDOMIMETIC WHICH ANTAGONIZES BOTH H- AND K-RAS ONCOGENIC SIGNALING.IC50 VALUE:TARGET: FTA 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 4.7 MG/ML
FTI-277 HCL IS AN INHIBITOR OF FARNESYL TRANSFERASE (FTASE) A HIGHLY POTENT RAS CAAX PEPTIDOMIMETIC WHICH ANTAGONIZES BOTH H- AND K-RAS ONCOGENIC SIGNALING.IC50 VALUE:TARGET: FTA 1 * 10 mg