TALABOSTAT (MESYLATE) [150080-09-4] 1 * 10 mg
Supplier: MEDCHEMEXPRESS
TALABOSTAT (MESYLATE) [150080-09-4] 1 * 10 mg
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LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 31 MG/ML
ACALABRUTINIB (ACP-196) IS A SECOND-GENERATION, SELECTIVE, IRRE VERSIBLE INHIBITOR OF BTK (BRUTON'S TYROSINE KINASE) THAT HAS IMPROVED PHARMACOLOGIC FEATURES, INCLUDING FAVORABLE PL 1 * 50 mg
Supplier: MEDCHEMEXPRESS
LIQUID FORMAT IS 10MM*1ML IN DMSO
SOLUBILITY: DMSO: ≥ 31 MG/ML
ACALABRUTINIB (ACP-196) IS A SECOND-GENERATION, SELECTIVE, IRRE VERSIBLE INHIBITOR OF BTK (BRUTON'S TYROSINE KINASE) THAT HAS IMPROVED PHARMACOLOGIC FEATURES, INCLUDING FAVORABLE PL 1 * 50 mg
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Baricitinib (10 mM * 1 mL in DMSO) 1 * 1 mL
Supplier: MEDCHEMEXPRESS
Baricitinib (10 mM * 1 mL in DMSO) 1 * 1 mL
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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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5-fluoro-N-{2-[(2S)-1-methyl-2-pyrrolidi 1 * 5 mg
Supplier: MEDCHEMEXPRESS
5-fluoro-N-{2-[(2S)-1-methyl-2-pyrrolidi 1 * 5 mg
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Inobrodib (CCS1477) 1 mg 1 * 1 mg
Supplier: MEDCHEMEXPRESS
Inobrodib (CCS1477) 1 mg 1 * 1 mg
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N-[(3R)-3-(2-chloro-5-fluorophenyl)-6-(5-cyano[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-oxo-2,3-dihydro-1H-isoindol-4-yl]-3-fluoro-5-(tr ifluoromethyl)benzamide 1 * 50 mg
Supplier: MEDCHEMEXPRESS
N-[(3R)-3-(2-chloro-5-fluorophenyl)-6-(5-cyano[1,2,4]triazolo[1,5-a]pyridin-6-yl)-1-oxo-2,3-dihydro-1H-isoindol-4-yl]-3-fluoro-5-(tr ifluoromethyl)benzamide 1 * 50 mg
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Exatecan (10 mM * 1 mL in DMSO ready for reconstitution) 1 * 1 g
Supplier: MEDCHEMEXPRESS
Exatecan (10 mM * 1 mL in DMSO ready for reconstitution) 1 * 1 g
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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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MedChemExpress:Risdiplam, 1 x 5 mg 1 * 5 mg
Supplier: MEDCHEMEXPRESS
MedChemExpress:Risdiplam, 1 x 5 mg 1 * 5 mg
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FORODESINE HYDROCHLORIDE 1 * 25 mg
Supplier: MEDCHEMEXPRESS
FORODESINE HYDROCHLORIDE 1 * 25 mg
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OSU-03012 (Synonyms: AR-12 PDK1 inhibitor AR-12) 1ml 10mM solution 1 * 1 mL
Supplier: MEDCHEMEXPRESS
OSU-03012 (Synonyms: AR-12 PDK1 inhibitor AR-12) 1ml 10mM solution 1 * 1 mL
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MS21 AKT degrader 1mg 1 * 1 mg
Supplier: MEDCHEMEXPRESS
MS21 AKT degrader 1mg 1 * 1 mg
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proTAME, a cell-permeable proagent form of TAME, is an anaphase promoting complex/cyclosome (APC/C) inhibitor. proTAME causes cell c ycle arrest in metaphase[1][2]. 1 * 50 mg
Supplier: MEDCHEMEXPRESS
proTAME, a cell-permeable proagent form of TAME, is an anaphase promoting complex/cyclosome (APC/C) inhibitor. proTAME causes cell c ycle arrest in metaphase[1][2]. 1 * 50 mg
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Raleukin (AMG-719) is a recombinant, nonglycosylated human interleukin-1 receptor (IL-1R) antagonist. Raleukin (AMG-719) is the firs t biological agent to block the pro-inflammatory effects[1][2]. 1 * 50 mg
Supplier: MEDCHEMEXPRESS
Raleukin (AMG-719) is a recombinant, nonglycosylated human interleukin-1 receptor (IL-1R) antagonist. Raleukin (AMG-719) is the firs t biological agent to block the pro-inflammatory effects[1][2]. 1 * 50 mg
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FGF-2 is a member of the fibroblast family involved in bone healing, cartilage repair, bone repair, and nerve regeneration. FGF-2 is also a mitotic promoter that accelerates cell proliferation. FGF-2 regulates immune processes by specifically target 1 * 1 Each
Supplier: MEDCHEMEXPRESS
FGF-2 is a member of the fibroblast family involved in bone healing, cartilage repair, bone repair, and nerve regeneration. FGF-2 is also a mitotic promoter that accelerates cell proliferation. FGF-2 regulates immune processes by specifically target 1 * 1 Each
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Fmoc-Glu-(Boc)-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. 1 * 25 mg
Supplier: MEDCHEMEXPRESS
Fmoc-Glu-(Boc)-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. 1 * 25 mg
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Zanubrutinib (BGB-3111) is a selective and orally active Bruton tyrosine kinase (Btk) inhibitor (IC50: 0.3 nM)[1][2]. 1 * 5 mg
Supplier: MEDCHEMEXPRESS
Zanubrutinib (BGB-3111) is a selective and orally active Bruton tyrosine kinase (Btk) inhibitor (IC50: 0.3 nM)[1][2]. 1 * 5 mg
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Salcaprozate sodium (SNAC), an oral absorption promoter, and has the potential as a delivery agent for oral forms of heparin and ins ulin. Salcaprozate sodium could increase passive transcellular permeation across small intestinal epithelia based on 1 * 250 mg
Supplier: MEDCHEMEXPRESS
Salcaprozate sodium (SNAC), an oral absorption promoter, and has the potential as a delivery agent for oral forms of heparin and ins ulin. Salcaprozate sodium could increase passive transcellular permeation across small intestinal epithelia based on 1 * 250 mg
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Rosopatamab (HuJ591) is a humanized antiPSMA IgG1 monoclonal antibody that can be used in cancer research, especially prostate cance r. Rosopatamab can be linked to the low-energy beta-emitting radioisotope lutetium-177 (177Lu) through the bifunction 1 * 5 mg
Supplier: MEDCHEMEXPRESS
Rosopatamab (HuJ591) is a humanized antiPSMA IgG1 monoclonal antibody that can be used in cancer research, especially prostate cance r. Rosopatamab can be linked to the low-energy beta-emitting radioisotope lutetium-177 (177Lu) through the bifunction 1 * 5 mg
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Azeliragon (TTP488) is an orally bioavailable inhibitor of the receptor for advanced glycation end products (RAGE) in development as a potential treatment to slow disease progression in patients with mild Alzheimer’s disease (AD)[1]. Azeliragon also 1 * 100 mg
Supplier: MEDCHEMEXPRESS
Azeliragon (TTP488) is an orally bioavailable inhibitor of the receptor for advanced glycation end products (RAGE) in development as a potential treatment to slow disease progression in patients with mild Alzheimer’s disease (AD)[1]. Azeliragon also 1 * 100 mg
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Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) is a selective and cell permeable caspase-8 inhibitor[1]. Z-IETD-FMK is also a granzyme B inhibito r[5]. 1 * 5 mg
Supplier: MEDCHEMEXPRESS
Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) is a selective and cell permeable caspase-8 inhibitor[1]. Z-IETD-FMK is also a granzyme B inhibito r[5]. 1 * 5 mg
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Taselisib (GDC-0032) is a potent PI3K inhibitor targets PIK3CA mutations, with Kis of 0.12 nM, 0.29 nM, 0.97 nM, and 9.1 nM for PI3K δ, PI3Kα, PI3Kγ and PI3Kβ, respectively. 1 * 200 mg
Supplier: MEDCHEMEXPRESS
Taselisib (GDC-0032) is a potent PI3K inhibitor targets PIK3CA mutations, with Kis of 0.12 nM, 0.29 nM, 0.97 nM, and 9.1 nM for PI3K δ, PI3Kα, PI3Kγ and PI3Kβ, respectively. 1 * 200 mg
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Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CO-CH3 (compound DC-13-C) is an intermediate in the synthesis of Exatecan (HY-13631) derivatives[1]. 1 * 100 mg
Supplier: MEDCHEMEXPRESS
Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CO-CH3 (compound DC-13-C) is an intermediate in the synthesis of Exatecan (HY-13631) derivatives[1]. 1 * 100 mg
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UCL-TRO-1938 is a potent allosteric activator of PI3Kα with an EC50 value of approximately 60 μM. UCL-TRO-1938 can induce cell proli feration and has cardioprotective and neural regeneration effects[1]. 1 * 25 mg
Supplier: MEDCHEMEXPRESS
UCL-TRO-1938 is a potent allosteric activator of PI3Kα with an EC50 value of approximately 60 μM. UCL-TRO-1938 can induce cell proli feration and has cardioprotective and neural regeneration effects[1]. 1 * 25 mg
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Catecholamine neurotransmitter, D2 dopamine receptor agonist Dopamine (TH) 10mg 1 * 10 mg
Supplier: MEDCHEMEXPRESS
Catecholamine neurotransmitter, D2 dopamine receptor agonist Dopamine (TH) 10mg 1 * 10 mg
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AZD4573 is a potent and highly selective CDK9 inhibitor (IC50 of [1]. 1 * 5 mg
Supplier: MEDCHEMEXPRESS
AZD4573 is a potent and highly selective CDK9 inhibitor (IC50 of [1]. 1 * 5 mg
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Cabozantinib is a potent and orally active inhibitor of VEGFR2 and MET, with IC50 values of 0.035, and 1.3 nM, respectively. Cabozan tinib displays strong inhibition of KIT, RET, AXL, TIE2, and FLT3 (IC50=4.6, 5.2, 7, 14.3, and 11.3 nM, respectively) 1 * 10 mg
Supplier: MEDCHEMEXPRESS
Cabozantinib is a potent and orally active inhibitor of VEGFR2 and MET, with IC50 values of 0.035, and 1.3 nM, respectively. Cabozan tinib displays strong inhibition of KIT, RET, AXL, TIE2, and FLT3 (IC50=4.6, 5.2, 7, 14.3, and 11.3 nM, respectively) 1 * 10 mg
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Nirmatrelvir (PF-07321332) is a potent and orally active SARS-CoV 3C-like protease (3CLPRO) inhibitor. Nirmatrelvir (PF-07321332) ta rgets to the SARS-CoV-2 virus and can be used for COVID-19 research[1]. 1 * 50 mg
Supplier: MEDCHEMEXPRESS
Nirmatrelvir (PF-07321332) is a potent and orally active SARS-CoV 3C-like protease (3CLPRO) inhibitor. Nirmatrelvir (PF-07321332) ta rgets to the SARS-CoV-2 virus and can be used for COVID-19 research[1]. 1 * 50 mg