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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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T11165EGLU；化合物 T11165(2S)-α-EGLU|||(2S)-α-Ethylglutamic acid；(2S)-α-EGLU|||(2S)-α-Ethylglutamic acid
EGLU, also known as (2S)-α-Ethylglutamic acid or (2S)-α-EGLU, is a potent and competitive antagonist of the mGluR-2 receptor, demonstrating a Kd value of 66 μM when interacting with the (lS,3S)-ACPD-sensitive site. This chemical compound functions as an antidepressant agent.
价 格：￥电议型 号：T11165产 地：中国大陆
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T11048LDIPQUO hydrochloride；化合物DIPQUO盐酸盐DIPQUO hydrochloride(1269365-82-3 Free base)；DIPQUO hydrochloride(1
DIPQUO hydrochloride is an activator of the bone marker alkaline phosphatase (ALP), with an EC50 of 6.27 μM in C2C12 cells. DIPQUO hydrochloride promotes mouse and human osteoblast differentiation via activation of p38 MAPK-β.
价 格：￥电议型 号：T11048L产 地：中国大陆
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T10965DBPR112；化合物DBPR112DBPR112
DBPR112 is an orally active furanopyrimidine-based EGFR inhibitor with IC50s of 15 nM and 48 nM for EGFRWT and EGFRL858R/T790M, respectively. DBPR112 can occupy the ATP-binding site. DBPR112 has significant antitumor efficacy.
价 格：￥电议型 号：T10965产 地：中国大陆
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T10865LCot inhibitor-1 hydrochloride；化合物Cot inhibitor-1盐酸盐Cot inhibitor-1 hydrochloride(915365-57-0 Free ba
Cot inhibitor-1 hydrochloride is an inhibitor of tumor progression loci-2 kinase (IC50 = 28 nM) and inhibits the production of TNF-α in human whole blood (IC50 = 5.7 nM).
价 格：￥电议型 号：T10865L产 地：中国大陆
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T10865Cot inhibitor-1；Cot抑制剂-1Cot inhibitor 1|||Cot inhibitor1|||Cot inhibitor-1；0
Cot inhibitor-1 is a selective inhibitor of Cot protein kinase (also known as Tpl2 or MAP3K8) (IC50 at 28 nM). Cot inhibitor-1 inhibited TNF-alpha production in human whole blood with IC50 of 5.7 nM. Cot is involved in a variety of cellular signaling pathways, particularly those involved in inflammation and immune responses. Cot inactivate-1 inhibits Cot activity and may have potential therapeutic effects on rheumatoid arthritis, inflammatory bowel disease and some types of cancer.
价 格：￥电议型 号：T10865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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T10834CL656；化合物 T10834c-[2’FdAMP(S)-2’FdIMP(S)]；c-[2’FdAMP(S)-2’FdIMP(S)]
CL656 is a stimulator of interferon genes (STING) activator.
价 格：￥电议型 号：T10834产 地：中国大陆
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T10765Eragidomide；化合物 EragidomideCC-90009|||Cereblon modulator 1；CC-90009|||Cereblon modulator 1
Eragidomide (CC-90009; Cereblon modulator 1) is a cereblon (CRBN) E3 ligase modulator. Eragidomide specifically binds to CRBN, thereby affecting the activity of the ubiquitin E3 ligase complex.
价 格：￥电议型 号：T10765产 地：中国大陆
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T10756Cenicriviroc Mesylate；化合物 T10756TBR-652 Mesylate|||TAK-652 Mesylate；TBR-652 Mesylate|||TAK-652 Mesyl
Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2 with anti-inflammatory and antiinfective activity.
价 格：￥电议型 号：T10756产 地：中国大陆
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T10719CCT365623 hydrochloride；化合物 T10719CCT365623 hydrochloride
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF.
价 格：￥电议型 号：T10719产 地：中国大陆
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T10694CB1 inverse agonist 1；化合物CB1 inverse agonist 1MRL-650；MRL-650
CB1 inverse agonist 1 (MRL-650) is an orally active and selective CB1 agonist. The IC50s for CB1 and CB2 are 7.5 nM and 4100 nM, respectively. CB1 inverse agonist 1 shows anorexigenic effects.
价 格：￥电议型 号：T10694产 地：中国大陆
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T10665Calcium-Sensing Receptor Antagonists I；化合物 T10665Calcium-Sensing Receptor Antagonists I
Calcium-Sensing Receptor Antagonists I functions as an antagonist to the parathyroid hormone receptors that sense calcium.
价 格：￥电议型 号：T10665产 地：中国大陆
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T10659Ca2+ channel agonist 1；化合物Ca2+ channel agonist 1Ca2+ channel agonist 1
Ca2+ channel agonist 1 is an agonist of N-type Ca2+ channel and an inhibitor of Cdk2 (EC50s: 14.23 μM and 3.34 μM) and is used as a potential treatment for motor nerve terminal dysfunction.
价 格：￥电议型 号：T10659产 地：中国大陆
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T10658CA inhibitor 1；化合物 T10658GS-6207 analog；GS-6207 analog
CA inhibitor 1 (GS-6207 analog) is a potent inhibitor of the HIV capsid.
价 格：￥电议型 号：T10658产 地：中国大陆
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T10657C75；化合物C75C-75；C-75
C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).
价 格：￥电议型 号：T10657产 地：中国大陆
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T10656trans-C75；反-4-羧基-5-辛基-3-甲基-丁内酯(±)-C75；(±)-C75|||反-4-羧基-5-辛基-3-甲基-丁内酯
trans-C75 ((±)-C75) is an enantiomer of C75. C75 is an inhibitor of fatty-acid synthase (FASN).
价 格：￥电议型 号：T10656产 地：中国大陆
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T10655c-Met inhibitor 1化合物c-Met inhibitor 13-[(2-甲基-2H-吲唑-5-基)硫基]-6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪
c-Met inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including glioblastoma, gastric, and pancreatic cancer.
价 格：￥电议型 号：T10655产 地：中国大陆
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T10654c-Met-IN-2；化合物 T10654c-Met-IN-2
c-Met-IN-2 is a selective and orally available c-Met inhibitor (IC50: 0.6 nM) with antitumor activity.
价 格：￥电议型 号：T10654产 地：中国大陆
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T10653c-met-IN-1；化合物 T10653c-met-IN-1
c-met-IN-1 is a potent and selective c-Met inhibitor (IC50: 1.1 nM) with antitumor activity.
价 格：￥电议型 号：T10653产 地：中国大陆
