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T11379GDC-0834；化合物 T11379GDC-0834
GDC-0834 inhibits BTK with an in vitro IC50 of 5.9 and 6.4 nM in biochemical and cellular assays, respectively, and in vivo IC50 of 1.1 and 5.6 μM in mouse and rat, respectively. GDC-0834 is a potent and selective BTK inhib
价 格：￥电议型 号：T11379产 地：中国大陆
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T11279FGFR1/DDR2 inhibitor 1；化合物FGFR1/DDR2 inhibitor 1FGFR1/DDR2 inhibitor 1
FGFR1/DDR2 inhibitor 1 is an inhibitor of discoindin domain receptor 2 (DDR2) and fibroblast growth factor receptor 1 (FGFR1), with IC50 values of 31.1 nM, 108.4 nM and 3.2 nM for FGFR1, KG-1, and DDR2, respectively.
价 格：￥电议型 号：T11279产 地：中国大陆
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T11246Etoricoxib-d4；依托考昔 D4MK-0663 D4|||L-791456 D4|||Etoricoxib D4；MK-0663 D4|||依托考昔 D4|||L-791456 D4|||E
Etoricoxib D4 is a non steroidal anti-inflammatory agent, acting as a selective and orally active COX-2 inhibitor, with IC50s of 1.1 μM and 116 μM for COX-2 and COX-1 in human whole blood.Etoricoxib D4 is a deuterium labeled Etoricoxib.
价 格：￥电议型 号：T11246产 地：中国大陆
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T11179Elubrixin；化合物ElubrixinSB-656933；SB-656933
Elubrixin (SB-656933) inhibits neutrophil CD11b upregulation (IC50 of 260.7 nM) and shape change (IC50 of 310.5 nM). Elubrixin can be used for inflammatory diseases such as inflammatory bowel disease and airway inflammation. Elubrixin is a potent, selective, competitive, reversible and orally active CXCR2 antagonist and an IL-8 receptor antagonist.
价 格：￥电议型 号：T11179产 地：中国大陆
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T11154LEG01377 2HCl；EG01377二盐酸盐EG01377 2HCl(2227996-00-9 Free base)；EG01377 2HCl(2227996-00-9 Free base)
EG01377 2HCl is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1) with a Kd value of 1.32 μM and an IC50 value of 609 nM for both EG01377 2HCl against NRP1-a1 and NRP1-b1.EG01377 exhibits anti-angiogenic, antimigratory and antitumor activities.
价 格：￥电议型 号：T11154L产 地：中国大陆
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T11105DS88790512；化合物 T11105DS88790512
DS88790512, IC50 at 11 nM, is an effective, selective, oral bioeffective TRPC6 inhibitor.
价 格：￥电议型 号：T11105产 地：中国大陆
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T1108Nithiamide；醋胺硝唑Aminitrozole|||CL-5279；Aminitrozole|||醋胺硝唑|||CL-5279
Nithiamide (CL-5279) is an orally available antiprotozoan agent used in the treatment of vaginal trichomoniasis.
价 格：￥电议型 号：T1108产 地：中国大陆
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T11079NMI 8739；化合物NMI 8739n-docosahexaenoyl dopamine|||Dha-DA conjugate；n-docosahexaenoyl dopamine|||Dha-D
NMI 8739 (n-docosahexaenoyl dopamine) is an agonist of D2 autoreceptor. NMI 8739 reduces NO production and elicits concentration-dependent suppression of CCL-20, MCP-1 and IL-6 release.
价 格：￥电议型 号：T11079产 地：中国大陆
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T10979DCPIB；化合物DCPIBDCPIB
DCPIB, a known specific and potent inhibitor of volume-regulated anion channels (VRAC),DCPIB displayed superior selectivity toward TRESK with an IC50 of 0.14 μM, demonstrating at least 100-fold higher affinity over TREK1/TRAAK channels.
价 格：￥电议型 号：T10979产 地：中国大陆
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T10937LD-JNKI-1 acetate；化合物D-JNKI-1 acetateD-JNKI-1 acetate(1445179-97-4 Free base)|||AM-111 acetate；D-JNKI
D-JNKI-1 acetate (AM-111 acetate) is a highly potent and cell-permeable peptide inhibitor of JNK.
价 格：￥电议型 号：T10937L产 地：中国大陆
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T10840LCM-579；化合物CM-579CM-579
CM-579 is a dual inhibitor of G9a and DNMT( IC50:16 nM, 32 nM for G9a and DNMT). It has potent in vitro cellular activity in a wide range of cancer cells.
价 格：￥电议型 号：T10840L产 地：中国大陆
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T10840CM-579 trihydrochloride (1846570-40-8 free base)；化合物 T10840CM-579 trihydrochloride；CM-579 trihydroch
CM-579 trihydrochloride is a first-in-class reversible and dual inhibitor of G9a and DNMT (IC50s: 16 nM, 32 nM) with potent in vitro cellular activity in a wide range of cancer cells.
价 格：￥电议型 号：T10840产 地：中国大陆
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T1084Apramycin sulfate；硫酸安普霉素Nebramycin II|||Ai3-29795；Nebramycin II|||Ai3-29795|||硫酸安普霉素|||硫酸阿布拉霉素
Apramycin sulfate (Nebramycin II) is an aminoglycoside antibiotic.
价 格：￥电议型 号：T1084产 地：中国大陆
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T10796Chlormethiazole hydrochloride；氯美噻唑盐酸盐Clomethiazole hydrochloride；氯美噻唑盐酸盐|||Clomethiazole hydrochlori
Chlormethiazole hydrochloride is an anticonvulsant and sedative. It also has neuroprotective.
价 格：￥电议型 号：T10796产 地：中国大陆
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T10795Chlordantoin；氯登妥因Clodantoin；Clodantoin|||氯登妥因
Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment.
价 格：￥电议型 号：T10795产 地：中国大陆
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T10793CHK1 inhibitor；化合物 T10793GDC-0575 analog；GDC-0575 analog
CHK1 inhibitor (GDC-0575 analog) is a CHK1 inhibitor.
价 格：￥电议型 号：T10793产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride；化合物CHK1-IN-4盐酸盐CHK1-IN-4 hydrochloride（2120398-41-4 Free base）；CHK1-IN-4 hyd
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T10792CHK1-IN-4；化合物 T10792CHK1-IN-4
CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.
价 格：￥电议型 号：T10792产 地：中国大陆
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T10791CHK1-IN-3；化合物CHK1-IN-3CHK1-IN-3
CHK1-IN-3 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 0.4 nM).
价 格：￥电议型 号：T10791产 地：中国大陆
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T10790CHK1-IN-2；化合物 T10790CHK1-IN-2
CHK1-IN-2 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 6 nM).
价 格：￥电议型 号：T10790产 地：中国大陆
