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T7163PF-05175157ACC, Acetyl Coenzyme A Carboxylase,Acetyl-CoA Carboxylase,inhibit,Inhibitor,PF 05175157,P
PF 05175157 is an inhibitor of acetyl-CoA carboxylase 1 (ACC1) and ACC2 (IC50s = 27, 33, 23.5, and 50.4 nM for human ACC1, human ACC2, rat ACC1, and rat ACC2, respectively
价 格：￥电议型 号：T7163产 地：中国大陆
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T9744MP07-66MP07-66,MP0766,chronic lymphocytic leukemia,FTY720 analogue,Inhibitor,SET-PP2A complex,inhibi
MP07-66 is a novel FTY720-analog devoid of immunosuppressive effects leads to the reactivation of PP2A, which in turn triggers apoptosis of CLL cells.
价 格：￥电议型 号：T9744产 地：中国大陆
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T9027CA-4948rheumatoid,inflammation,CD135,inhibit,IL-1R associated kinase,CA4948,lymphoma,Interleukin-1 r
Emavusertib is a potent IRAK4/FLT3 inhibtor. CA-4948 with anti-tumor activity.
价 格：￥电议型 号：T9027产 地：中国大陆
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T8647BCH001PARN,dyskeratosis,telomerase,stem,BCH 001,polynucleotide,TERC,rPAPD5,ncRNA,BCH001,polymerases,
BCH001 is a specific small-molecule inhibitor of PAPD5.
价 格：￥电议型 号：T8647产 地：中国大陆
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T6S0619Pachymic acidPachymic acid,PKB,Protein kinase B,inhibit,Akt,ERK,Extracellular signal regulated kinas
Pachymic acid is a natural product, and inhibits Akt and ERK signaling pathways.
价 格：￥电议型 号：T6S0619产 地：中国大陆
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T9595LP-261NCI-H522,tubulin polymerization,tumor,SW-620,BXPC-3,H522,anti-mitotic,inhibit,LP261,MCF-7,Inhi
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
价 格：￥电议型 号：T9595产 地：中国大陆
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TQ0243ND-646Acetyl-CoA Carboxylase,ND 646,ND646,ND-646,ACC, Acetyl Coenzyme A Carboxylase,Inhibitor,inhibi
ND-646 is an orally bioavailable and allosteric inhibitor of the ACC enzymes ACC1 and ACC2(IC50s of 3.5 nM and 4.1 nM for recombinant hACC1 and hACC2, respectively)
价 格：￥电议型 号：TQ0243产 地：中国大陆
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T6578ME0328ME 0328,inhibit,poly ADP ribose polymerase,ME-0328,ME0328,PARP,Inhibitor
ME0328 is a potent and selective PARP inhibitor with IC50 of 0.89 μM for PARP3, about 7-fold selectivity over PARP1.
价 格：￥电议型 号：T6578产 地：中国大陆
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T7955EB-3Dlipid,inhibit,lymphoblastic,AMP-activated protein kinase,EB3D,acute,tumorigenesis,Apoptosis,hom
EB-3D is a potent and selective choline kinase alpha 1 (ChoKα1) inhibitor(IC50 : 1 μM).with anti-cancer activity.
价 格：￥电议型 号：T7955产 地：中国大陆
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T6632RaltitrexedRaltitrexed,Thymidylate Synthase,D 1694,inhibit,Nucleoside Antimetabolite/Analog,ZD-1694,
Raltitrexed（IC50 of 9 nM）, a thymidylate synthase inhibitor, is used for the inhibition of L1210 cell growth.
价 格：￥电议型 号：T6632产 地：中国大陆
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T6614Nutlin-3bNutlin 3b,Inhibitor,MDM-2/p53,Ubiquitin activating enzyme,Ubiquitin conjugating enzyme,inhi
Nutlin-3b is a p53/MDM2 antagonist or inhibitor (IC50: 13.6 μM), 150-fold less potent (+)-enantiomer of Nutlin-3 as in comparison with opposite (-)-enantiomer Nutlin-3a.
价 格：￥电议型 号：T6614产 地：中国大陆
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T9464CYM50358CYM50358,LPL Receptor,Lysophospholipid Receptor,CYM-50358,Inhibitor,CYM 50358,inhibit,S1PR4
N-(4-(aminomethyl)-2,6-dimethylphenyl)-5 is a potent, selective antagonist of the sphingosine-1-phosphate receptor 4 (S1P4). CYM50358 inhibits S1P4?with an IC50?of 25 nM.
价 格：￥电议型 号：T9464产 地：中国大陆
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T8527CPYPPDOCK2,CPYPP,Inhibitor,GEF,Rac1,DOCK180,lymphocytes,autoimmune,DOCK2-Rac1,inhibit,DOCK5,immunosu
CPYPP is an inhibitor of DOCK2-Rac1 interaction. CPYPP binds to DOCK2 DHR-2 domain and inhibits the guanine nucleotide exchange factor (GEF) activity of DOCK2DHR-2 for Rac1 in a dose-dependent manner(IC50 : 22.8 μM). CPYPP also inhibits DOCK180, DOCK5 and less DOCK9
价 格：￥电议型 号：T8527产 地：中国大陆
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T86955-Hydroxymethyldeoxyuridine5 Hydroxymethyldeoxyuridine,5Hydroxymethyldeoxyuridine
5-Hydroxymethyldeoxyuridine is an analog of nucleoside that has anticancer and antiviral activities. It suppresses the replication of murine S180 lung carcinoma cells and Ehrlich ascites mammary carcinoma cells (ED50s = 8.5 and 4 μM, respectively) and multiple human leukemia cell lines (IC50s = 1.7-5.8 μM).
价 格：￥电议型 号：T8695产 地：中国大陆
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T11940Malic enzyme inhibitor ME1
Malic enzyme inhibitor ME1 is a specific inhibitor of Malic enzyme (IC50 = 0.15 μM). Malic enzyme inhibitor ME1 reduces cell viability/metabolic activity.
价 格：￥电议型 号：T11940产 地：中国大陆
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T7212Delavirdine mesylatepolymerase,BHAP-U 90152,U90152,U 90152,Inhibitor,Reverse Transcriptase,Delavirdi
Delavirdine (mesylate) is a non-nucleoside reverse transcriptase inhibitor (NNRTI).
价 格：￥电议型 号：T7212产 地：中国大陆
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TD0099Malachite green oxalatephosphate,p65,IKK,Nuclear factor-kappaB,NF-κB,IKBKE,enzymatic,Malachite green
Malachite green oxalate is a triphenylmethane dye which can be used to detect the release of phosphate in enzymatic reactions.
价 格：￥电议型 号：TD0099产 地：中国大陆
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T8816NAE-IN-M22NAEINM22,cancer,Inhibitor,NAE-IN-M-22,NAE,NEDD8,NAE IN M22,enzyme,activating,inhibit,tumor
NAE-IN-M22 is a selective, potent and reversible inhibitor of NEDD8 activating enzyme (NAE). NAE-IN-M22 inhibits multiple cancer cell lines and induces apoptosis in A549 cells. NAE-IN-M22 also can inhibit tumor growth in vivo.
价 格：￥电议型 号：T8816产 地：中国大陆
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T6941PI-1840cell proliferation,Proteasome,Caspase,proteasome substrates,poly ADP ribose polymerase,inhibi
PI-1840（ IC50 = 27 nM）is a reversible and selective chymotrypsin-like (CT-L) inhibitor, with little proteasome proteolytic effects on trypsin-like (T-L) and postglutamyl-peptide-hydrolysis-like (PGPH-L).
价 格：￥电议型 号：T6941产 地：中国大陆
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T99984H-1,2,4-Triazole, 3-(phenoxymethyl)-4-phenyl-5-[(phenylmethyl)thio]-Huntington’s disease,4H 1,2,4 T
4H-1,2,4-Triazole, 3-(phenoxymethyl)-4-phenyl-5-[(phenylmethyl)thio]- is an inhibitor of SIRT2 with antitumor activity.
价 格：￥电议型 号：T9998产 地：中国大陆
