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产品目录

编号化学名称Cas号纯度化学结构
25146Chiauranib1256349-48-098% Min.
Chiauranib also known as orally available, small molecule inhibitor of select serine-
251282-氯-3-氟-4-吡啶甲醇946127-54-4≧98.0%
25078CFT19462882165-79-7≧98.0%
CFT1946 是一种口服生物可利用的小分子降解剂,可降解实体瘤中的
25045Cavosonstat1371587-51-798% Min.
Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
25041CC-900031621999-82-398% Min.
CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E
24161CMP-5 2HCl2309409-79-698% Min.
CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
24156CYD192415281-52-498% Min.
CYD19 is a potent Snail/HDAC dual target inhibitor.
24144CPI-455 HCl2095432-28-198% Min.
CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
24109CBR-5884681159-27-3≧98.0%
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
24101Crelosidenib2230263-60-0≧98.0%
Crelosidenib ( [LY3410738)是一种有效的选择性的具有口服活性的突变
24095CC90001 free base1403859-14-298% Min.
CC-90001 is a potent and selective JNK inhibitor, which is 12.9-fold more potent for
24064Cirtuvivint ( SM08502 )2143917-62-6≧98.0%
Cirtuvivint是一种CDC样激酶(CLK)和双特异性酪氨酸磷酸化调节激酶
24052Camonsertib2417489-10-098% Min.
Camonsertib, also known as RP 3500, is aA Novel, Potent, and Selective ATR Inhibitor
24024CVN-2932815296-08-1≧98.0%
CVN-293是一种口服、脑渗透性、KCNK13小分子抑制剂。
240225-氯-2-甲氧基吡啶-3-磺酰氯1261451-92-6≧98.0%
5-氯-2-甲氧基吡啶-3-磺酰氯, CAS 1261451-92-6.
20678CUR5g1370032-20-498% Min.
CUR5g is a potent autophagy inhibitor.
20653Contezolid free base1112968-42-998% Min.
Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i
20645CP-506 ( Synonyms: SN-36506 )2227304-19-898% Min.
CP-506 (SN-36506) 是一种缺氧激活的 DNA 烷基化氮芥化合物前药,能够
20632Censavudine634907-30-598% Min.
Censavudine, also known as OBP-601, BMS-986001 or festinavir, is a nucleoside reverse
20626CFI-402257 free base1610759-22-298% Min.
CFI-402257 was discontinued for commercial reason.
20622Cantharidine56-25-798% Min.
Cantharidine (free base) is a PP1/2A inhibitor found in Canarthis vesicatoria. It inh
20575Compound E209986-17-498% Min.
Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch
205620990CL511514-03-798% Min.
0990CL is an inhibitor of heterotrimeric Gαi subunits. 0990CL showed direct interact
20558CBiPES HCl856702-40-498% Min.
CBiPES HCl is a selective positive allosteric modulator of the mGlu2 receptor.
20555COH1 inhibitor20217-22-598% Min.
COH1 is a ribonucleotide reductase (RR) inhibitor.
20510CC-92480 ( Mezigdomide )2259648-80-9≧98.0%
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
20488CYM-503081345858-76-598% Min.
CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity
20478CRANAD-281623747-97-698% Min.
CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts
20467CPPHA693288-97-098% Min.
CPPHA is a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5
20455Camlipixant ( BLU-5937 )1621164-74-6≧98.0%
Camlipixant 是一种在研的每日两次口服 P2X3 受体拮抗剂,用于治疗