"MEDCHEMEXPRESS"

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MEDCHEM EXPRESS SLX 2119 ROCK INHIBITOR KD-025 1 * 5 mg

Supplier: MEDCHEMEXPRESS

MEDCHEM EXPRESS SLX 2119 ROCK INHIBITOR KD-025 1 * 5 mg

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NX-5948-98% 1 * 10 mg

Supplier: MEDCHEMEXPRESS

NX-5948-98% 1 * 10 mg

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SN-38 1 * 500 mg

Supplier: MEDCHEMEXPRESS

SN-38 1 * 500 mg

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LIQUID FORMAT IS 10MM1ML IN DMSO
SOLUBILITY: DMSO 58 MG/ML WATER <1 MG/ML
GO 6983 IS A PAN-PKC INHIBITOR AGAINST FOR PKCΑ, P KCΒ, PKCΓ AND PKCΔ WITH IC50 OF 7 NM, 7 NM, 6 NM AND 10 NM, RESPECTIVELY LESS POTENT TO PKCΖ AND INACTIVE TO PKCΜ.IC 1 10 mg

Supplier: MEDCHEMEXPRESS

LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 58 MG/ML WATER <1 MG/ML
GO 6983 IS A PAN-PKC INHIBITOR AGAINST FOR PKCΑ, P KCΒ, PKCΓ AND PKCΔ WITH IC50 OF 7 NM, 7 NM, 6 NM AND 10 NM, RESPECTIVELY LESS POTENT TO PKCΖ AND INACTIVE TO PKCΜ.IC 1 * 10 mg

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LIQUID FORMAT IS 10MM1ML 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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Remdesivir 1 * 5 mg

Supplier: MEDCHEMEXPRESS

Remdesivir 1 * 5 mg

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LIQUID FORMAT IS 10MM1ML 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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Rotenone 1 * 1 g

Supplier: MEDCHEMEXPRESS

Rotenone 1 * 1 g

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LIQUID FORMAT IS 10MM1ML 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 10MM1ML 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