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产品目录

编号化学名称Cas号纯度化学结构
16122717MK-4827(Niraparib) tosylate1038915-73-998% 
MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8
6111524MP-A08219832-49-298% 
MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S
6111404Mcl1-IN-2292057-76-298% 
Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value.
6111403Marinopyrrole A1227962-62-098% 
Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value
61116ML2241338824-21-798% 
ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula
61114(±)-Methotrimeprazine D61189805-51-398% 
()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d
6111017Motolimod926927-61-998% 
Motolimod
6111014MCC950 sodium256373-96-398% 
MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w
6111012MS0231831110-54-398% 
MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC
6111008MK-4101935273-79-398% 
MK-4101 is a potent SMO Inhibitor of the Hedgehog PathwayMK-4101 is a potent SMO Inhi
611940ML346100872-83-198% 
ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.
611820mTOR-IN-11207358-59-598% 
mTOR-IN-1 is a potent and selective ATP-competitive inhibitor of mTOR with Ki of 1.5
161009023Miltefosine58066-85-698% by HPLC 
Miltefosine targets cellular membranes, modulating cell membrane permeability, membra
1697011-METHYL-5-NITRO-1H-INDOLE29906-67-098% by HNMR/HPLC 
1-METHYL-5-NITRO-1H-INDOLE CAS#29906-67-0
16071022Mubritinib366017-09-698% by HPLC 
Mubritinib, also known as TAK-165, is a protein kinase inhibitor which was under deve
16070814MK-82451030612-87-398% by HPLC 
MK-8245
16070813MLN120B783348-36-798% by HPLC 
MLN120B
16070106MS417916489-36-698% by HPLC 
MS417, also known as GTPL7512, is a potent and selective BRD4 inhibitor. MS417 inhibi
16062901Molidustat (BAY85-3934)1154025-82-698% by HPLC 
Molidustat (BAY85-3934)
1662118MK-8931 ( Verubecestat )1286770-55-598% by HPLC/HNMR 
MK-8931(verubecestat)是一种BACE抑制剂,是由默沙东公司研制开发。主
16062101Methyl 2,5-dimethylnicotinate63820-72-498% by HPLC 
Methyl 2,5-dimethylnicotinate
16060603MDK-52201796565-52-098% by HPLC 
MDK-5220 exhibits an orexin agonist activity and is expected to be useful as an excel
032514MK-51721350514-68-998% 
Coming soon!
030904Mirodenafil862189-95-598% 
Coming soon!
030901MK-28661202044-20-998% 
Coming soon!
030101MCC950210826-40-798% 
MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM
020106MRE-269475085-57-598% 
MRE-269 is a long-acting and highly selective prostacyclin receptor agonist.
011906MSX-122897657-95-398% 
MSX-122 is a n orally bioavailable inhibitor of CXCR4 with potential antineoplastic a
011902ME-143852536-39-198% 
ME -143 is a derivative of triphendiol and is a highly potent, pan acting ant-cancer.
011805MK-22061032349-93-198% 
MK-2206 2Hcl is an orally bioavailable allosteric inhibitor of the serine/threonine p