"MEDCHEMEXPRESS"
SCD1 inhibitor Icomidocholic acid 1 * 1 mL
Supplier: MEDCHEMEXPRESS
SCD1 inhibitor Icomidocholic acid 1 * 1 mL
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥10MG/ML WATER <1.2MG/ML ETHANOL <1.2MG/ML
NILOTINIB (AMN-107) IS A BCR-ABL INHIBITOR WITH IC50 LESS THAN 30 NM.IC50 VALUE: < 30 NM [1]TARGET: BCR-ABLIN VITRO: NILOTINIB (AMN107) IS SIGNIFICAN 1 * 100 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO ≥10MG/ML WATER <1.2MG/ML ETHANOL <1.2MG/ML
NILOTINIB (AMN-107) IS A BCR-ABL INHIBITOR WITH IC50 LESS THAN 30 NM.IC50 VALUE: < 30 NM [1]TARGET: BCR-ABLIN VITRO: NILOTINIB (AMN107) IS SIGNIFICAN 1 * 100 mg
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ANTI-HUMAN CD47 ANTIBODY URABRELIMAB 1 * 5 mg
Supplier: MEDCHEMEXPRESS
ANTI-HUMAN CD47 ANTIBODY URABRELIMAB 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 9.06 MG/ML
DUBS-IN-2 IS A POTENT DEUBIQUITINASE ENZYME INHIBITOR WITH IC 50S OF 7.2 UM/0.93 UM FOR USP7/USP8 RESPECTIVELY.IC50 VALUE: 7.2 UM/0.93 UM(USP7/USP8) [1]TARGET: USP7/USP8 1 * 1 mL
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 9.06 MG/ML
DUBS-IN-2 IS A POTENT DEUBIQUITINASE ENZYME INHIBITOR WITH IC 50S OF 7.2 UM/0.93 UM FOR USP7/USP8 RESPECTIVELY.IC50 VALUE: 7.2 UM/0.93 UM(USP7/USP8) [1]TARGET: USP7/USP8 1 * 1 mL
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ANTI-HUMAN CD47 ANTIBODY LIGUFALIMAB 1 * 5 mg
Supplier: MEDCHEMEXPRESS
ANTI-HUMAN CD47 ANTIBODY LIGUFALIMAB 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: 31MG/ML
A-1155463 IS A HIGHLY POTENT AND SELECTIVE BCL-XL INHIBITOR, A-115 5463 SHOWS PICOMOLAR BINDING AFFINITY TO BCL-XL (KI ＜0.01 NM), AND >1000-FOLD WEAKER BINDING TO BCL-2 (KI = 80 NM) AN 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: 31MG/ML
A-1155463 IS A HIGHLY POTENT AND SELECTIVE BCL-XL INHIBITOR, A-115 5463 SHOWS PICOMOLAR BINDING AFFINITY TO BCL-XL (KI ＜0.01 NM), AND >1000-FOLD WEAKER BINDING TO BCL-2 (KI = 80 NM) AN 1 * 10 mg
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TAK-243 450833-55-2 1 * 5 mg
Supplier: MEDCHEMEXPRESS
TAK-243 450833-55-2 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: IN DMSO > 10 MM
NBI-74330 IS A SMALL MOLECULE ANTAGONIST FOR CXCR3, NBI-74330 DE MONSTRATES POTENT INHIBITION OF [(125)I]CXCL10 AND [(125)I]CXCL11 SPECIFIC BINDING (K(I) OF 1.5 AND 3.2 NM, RESPECTIV 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: IN DMSO > 10 MM
NBI-74330 IS A SMALL MOLECULE ANTAGONIST FOR CXCR3, NBI-74330 DE MONSTRATES POTENT INHIBITION OF [(125)I]CXCL10 AND [(125)I]CXCL11 SPECIFIC BINDING (K(I) OF 1.5 AND 3.2 NM, RESPECTIV 1 * 5 mg
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TETRAHYDROFOLIC ACID 1 * 25 mg
Supplier: MEDCHEMEXPRESS
TETRAHYDROFOLIC ACID 1 * 25 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 49 MG/ML
SB1317(TG-02) IS A NOVEL SMALL MOLECULE POTENT CDK2/JAK2/FLT3 I NHIBITOR WITH IC50S OF 13/73/56 NM RESPECTIVELY.IC50 VALUE: 13/73/56 NM(CDK2/JAK2/FLT3) TARGET: CDK2/JAK2/FLT3TG02 IS 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 49 MG/ML
SB1317(TG-02) IS A NOVEL SMALL MOLECULE POTENT CDK2/JAK2/FLT3 I NHIBITOR WITH IC50S OF 13/73/56 NM RESPECTIVELY.IC50 VALUE: 13/73/56 NM(CDK2/JAK2/FLT3) TARGET: CDK2/JAK2/FLT3TG02 IS 1 * 10 mg
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diABZI STING agonist-1 trihydrochloride 1 * 10 mg
Supplier: MEDCHEMEXPRESS
diABZI STING agonist-1 trihydrochloride 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ＞ 27.5 MG/ML
VANDETANIB (ZD6474) IS A POTENT INHIBITOR OF VEGFR2 WITH IC50 OF 40 NM.IC50 VALUE: 40 NM (VEGFR2) [1]TARGET: VEGFR2VANDETANIB IS AN ANTI-CANCER DRUG THAT IS USED FOR THE TREATMEN 1 * 25 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ＞ 27.5 MG/ML
VANDETANIB (ZD6474) IS A POTENT INHIBITOR OF VEGFR2 WITH IC50 OF 40 NM.IC50 VALUE: 40 NM (VEGFR2) [1]TARGET: VEGFR2VANDETANIB IS AN ANTI-CANCER DRUG THAT IS USED FOR THE TREATMEN 1 * 25 mg