"MEDCHEMEXPRESS"
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO >20 MG/ML
UK-5099(PF1005023) IS A POTENT INHIBITOR OF PLASMA MEMBRANE MONOC ARBOXYLATE TRANSPORTERS (MCTS) AND THE MITOCHONDRIAL PYRUVATE CARRIER (MPC) INHIBITS PYRUVATE-DEPENDENT O2 CONSUMPTI 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO >20 MG/ML
UK-5099(PF1005023) IS A POTENT INHIBITOR OF PLASMA MEMBRANE MONOC ARBOXYLATE TRANSPORTERS (MCTS) AND THE MITOCHONDRIAL PYRUVATE CARRIER (MPC) INHIBITS PYRUVATE-DEPENDENT O2 CONSUMPTI 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
AUCUBIN IS AN IRIDOID GLYCOSIDE WITH A WIDE RANGE OF BIOLOGICAL AC TIVITIES, INCLUDING ANTI-INFLAMMATORY, ANTI-MICROBIAL, ANTI-ALGESIC AS WELL AS ANTI-TUMOR ACTIVITIES.IC50 VALUE:TARGE 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 10 MM IN DMSO
AUCUBIN IS AN IRIDOID GLYCOSIDE WITH A WIDE RANGE OF BIOLOGICAL AC TIVITIES, INCLUDING ANTI-INFLAMMATORY, ANTI-MICROBIAL, ANTI-ALGESIC AS WELL AS ANTI-TUMOR ACTIVITIES.IC50 VALUE:TARGE 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: > 9 MG/ML
HALOFUGINONE IS A PLANT DERIVATIVE THAT HAS BEEN SHOWN TO INHIBI T TH17 DIFFERENTIATION, AND RECENTLY TESTED AS A POTENTIAL IMMUNOSUPPRESSANT.IC50 VALUE:TARGET:IN VITRO: THE ADDITION 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: > 9 MG/ML
HALOFUGINONE IS A PLANT DERIVATIVE THAT HAS BEEN SHOWN TO INHIBI T TH17 DIFFERENTIATION, AND RECENTLY TESTED AS A POTENTIAL IMMUNOSUPPRESSANT.IC50 VALUE:TARGET:IN VITRO: THE ADDITION 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:> 10 MM
D609 IS A SELECTIVE COMPETITIVE PHOSPHATIDYL CHOLINE-SPECIFIC PHOSP HOLIPASE C (PC-PLC) INHIBITOR (KI = 6.4 ΜM) ANTIVIRAL AND ANTITUMOR AGENT. IC50 VALUE: 6.4 UM (KI)TARGET: PC-PLCD609 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:> 10 MM
D609 IS A SELECTIVE COMPETITIVE PHOSPHATIDYL CHOLINE-SPECIFIC PHOSP HOLIPASE C (PC-PLC) INHIBITOR (KI = 6.4 ΜM) ANTIVIRAL AND ANTITUMOR AGENT. IC50 VALUE: 6.4 UM (KI)TARGET: PC-PLCD609 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:≥ 21.5 MG/ML
XAV939 IS A SMALL MOLECULE AND SELECTIVE WNT PATHWAY Β-CATENIN -MEDIATED TRANSCRIPTION INHIBITOR AND AXIN STABILIZING AGENT WITH IC50 OF 11 AND 4 NM FOR THE INHIBITION OF TNKS1 AND 1 * 10 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO:≥ 21.5 MG/ML
XAV939 IS A SMALL MOLECULE AND SELECTIVE WNT PATHWAY Β-CATENIN -MEDIATED TRANSCRIPTION INHIBITOR AND AXIN STABILIZING AGENT WITH IC50 OF 11 AND 4 NM FOR THE INHIBITION OF TNKS1 AND 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 6 MG/ML WATER <1 MG/ML
NALIDIXIC ACID IS A SYNTHETIC 1,8-NAPHTHYRIDINE ANT IMICROBIAL AGENT WITH A LIMITED BACTERIOCIDAL SPECTRUM.TARGET: ANTIBACTERIALNALIDIXIC ACID IS THE FIRST OF THE SYNTHE 1 * 1 mL
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO 6 MG/ML WATER <1 MG/ML
NALIDIXIC ACID IS A SYNTHETIC 1,8-NAPHTHYRIDINE ANT IMICROBIAL AGENT WITH A LIMITED BACTERIOCIDAL SPECTRUM.TARGET: ANTIBACTERIALNALIDIXIC ACID IS THE FIRST OF THE SYNTHE 1 * 1 mL
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SOLUBILITY: 0.50 MG/ML IN H2O
ARGIPRESSIN IS A ANTIDIURETIC HORMONE THAT HAS BEEN FOUND IN MOST MAMMALIAN SPECIES. ALSO ACTS AS A NEUROTRANSMITTER AT SYNAPSES IN THE BRAIN INCREASES [CA2+]I IN CULTURED RAT HIPPOCAMPAL NEURONS. 1 * 10 mg
Supplier: MEDCHEMEXPRESS
SOLUBILITY: 0.50 MG/ML IN H2O
ARGIPRESSIN IS A ANTIDIURETIC HORMONE THAT HAS BEEN FOUND IN MOST MAMMALIAN SPECIES. ALSO ACTS AS A NEUROTRANSMITTER AT SYNAPSES IN THE BRAIN INCREASES [CA2+]I IN CULTURED RAT HIPPOCAMPAL NEURONS. 1 * 10 mg
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JH-X-119-01 HYDROCHLORIDE 1 * 5 mg
Supplier: MEDCHEMEXPRESS
JH-X-119-01 HYDROCHLORIDE 1 * 5 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 38 MG/ML IN DMSO
EHT 1864 IS A SMALL MOLECULE INHIBITOR OF RAC1 SIGNALING MODUL ATE Γ-SECRETASE-MEDIATED APP PROCESSING.IC50 VALUE:TARGET: RAC1 INHIBITORIN VITRO: EHT 1864 BLOCKS AΒ 40 AND AΒ 42 PR 1 * 5 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: 38 MG/ML IN DMSO
EHT 1864 IS A SMALL MOLECULE INHIBITOR OF RAC1 SIGNALING MODUL ATE Γ-SECRETASE-MEDIATED APP PROCESSING.IC50 VALUE:TARGET: RAC1 INHIBITORIN VITRO: EHT 1864 BLOCKS AΒ 40 AND AΒ 42 PR 1 * 5 mg
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