"MEDCHEMEXPRESS"
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 75 MG/ML WATER <1 MG/ML ETHANOL <1 MG/ML
BMN 673 IS A NOVEL PARP1/2 INHIB ITOR WITH IC50 OF 0.58 NM(PARP1) DOES NOT INHIBIT PARG AND IS HIGHLY SENSITIVE TO PTEN MUTATION. IC50 VALUE: 0.58 NM 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 75 MG/ML WATER <1 MG/ML ETHANOL <1 MG/ML
BMN 673 IS A NOVEL PARP1/2 INHIB ITOR WITH IC50 OF 0.58 NM(PARP1) DOES NOT INHIBIT PARG AND IS HIGHLY SENSITIVE TO PTEN MUTATION. IC50 VALUE: 0.58 NM 1 * 10 mg
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SOLUBILITY: DMSO ≥45MG/ML WATER <1.2MG/ML ETHANOL <1.2.MG/ML
VELIPARIB (ABT-888) IS A POTENT INHIBITOR OF PARP1 AND PARP2 WITH KI OF 5.2 NM AND 2.9 NM, RESPECTIVELY.IC50 VALUE: 5.2 NM(KI FOR PARP1) 2.9 NM(KI FOR PARP2) [1]TARGET: PARP1 PARP2IN I 1 * 50 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: DMSO ≥45MG/ML WATER <1.2MG/ML ETHANOL <1.2.MG/ML
VELIPARIB (ABT-888) IS A POTENT INHIBITOR OF PARP1 AND PARP2 WITH KI OF 5.2 NM AND 2.9 NM, RESPECTIVELY.IC50 VALUE: 5.2 NM(KI FOR PARP1) 2.9 NM(KI FOR PARP2) [1]TARGET: PARP1 PARP2IN I 1 * 50 mg
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7-Aminomethyl-10-methyl-11-fluoro camptothecin - 99.30% CAS No. : 2378616-23-8 1 * 5 mg
Supplier: MEDCHEMEXPRESS
7-Aminomethyl-10-methyl-11-fluoro camptothecin - 99.30% CAS No. : 2378616-23-8 1 * 5 mg
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DAGROCORAT HYDROCHLORIDE 1 * 5 mg
Supplier: MEDCHEMEXPRESS
DAGROCORAT HYDROCHLORIDE 1 * 5 mg
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SOLUBILITY: DMSO: ≥ 33 MG/ML
BI605906, A NOVEL INHIBITOR OF IKKΒ, INHIBITS IKKΒ WITH AN IC50 VALUE OF 380 NM WHEN ASSAYED AT 0.1 MM ATP. IC50 VALUE: 380 NMTARGET: IKKΒIN VITRO: BI605906 IS A NOVEL PHARMACOLOGICAL INHIBITORS OF THE IKK FAMILY, INHI 1 * 1 mL
Supplier: MEDCHEMEXPRESS
SOLUBILITY: DMSO: ≥ 33 MG/ML
BI605906, A NOVEL INHIBITOR OF IKKΒ, INHIBITS IKKΒ WITH AN IC50 VALUE OF 380 NM WHEN ASSAYED AT 0.1 MM ATP. IC50 VALUE: 380 NMTARGET: IKKΒIN VITRO: BI605906 IS A NOVEL PHARMACOLOGICAL INHIBITORS OF THE IKK FAMILY, INHI 1 * 1 mL
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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 * 5 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 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: 9 MG/ML, H2O: ＜ 1 MG/ML
CRIZOTINIB (PF-2341066) IS A POTENT INHIBITOR OF C -MET AND ALK WITH IC50 OF 11 NM AND 24 NM, RESPECTIVLEY.IC50 VALUE: 11 NM/24 NM (C-MET/ALK) [1]TARGET: C-MET/ALKIN VI 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: 9 MG/ML, H2O: ＜ 1 MG/ML
CRIZOTINIB (PF-2341066) IS A POTENT INHIBITOR OF C -MET AND ALK WITH IC50 OF 11 NM AND 24 NM, RESPECTIVLEY.IC50 VALUE: 11 NM/24 NM (C-MET/ALK) [1]TARGET: C-MET/ALKIN VI 1 * 10 mg
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Salcaprozate Sodium 1 * 5 g
Supplier: MEDCHEMEXPRESS
Salcaprozate Sodium 1 * 5 g
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Bleomycin hydrochloride 10 mM * 1 mL in DMSO 1 * 1 mL
Supplier: MEDCHEMEXPRESS
Bleomycin hydrochloride 10 mM * 1 mL in DMSO 1 * 1 mL
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2,3-Naphthalenediamine,98% 1 * 500 mg
Supplier: MEDCHEMEXPRESS
2,3-Naphthalenediamine,98% 1 * 500 mg
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D-Lin-MC3-DMA (98%) 1 * 1,5 g
Supplier: MEDCHEMEXPRESS
D-Lin-MC3-DMA (98%) 1 * 1,5 g