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Medical Research Areas
Stem Cells / Wnt
STAT
STAT
下级目录
STA 21
AZD-1208
BMS-911543
Birabresib
INCB16562
Azd-1480
PACRITINIB
H-GAMMA-D-GLU-TRP-OH
TYRPHOSTIN AG 490
目录项下的产品
111540-00-2 / MFCD11540002
8-Hydroxy-3-Methyl-3,4-Dihydrotetraphene-1,7,12(2H)-Trione
8-羟基-3-甲基-3,4-二氢苯并蒽-1,7,12(2H)-三酮
原料
0
资源
0.0
询
0.0
%成交
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试剂
1204144-28-4 / MFCD304144284
(R,Z)-5-((2-(3-Aminopiperidin-1-Yl)-[1,1'-Biphenyl]-3-Yl)Methylene)Thiazolidine-2,4-Dione
(R,Z)-5-((2-(3-氨基哌啶-1-基)-[1,1'-联苯]-3-基)亚甲基)噻唑烷-2,4-二酮
原料
0
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0.0
询
0.0
%成交
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试剂
1271022-90-2 / MFCD371022902
N,N-Dicyclopropyl-4-((1,5-Dimethyl-1H-Pyrazol-3-Yl)Amino)-6-Ethyl-1-Methyl-1,6-Dihydroimidazo[4,5-D]Pyrrolo[2,3-B]Pyridine-7-Carboxamide
N,N-二环丙基-4-((1,5-二甲基-1H-吡唑-3-基)氨基)-6-乙基-1,6-二氢-1-甲基-咪唑并[4,5-d]吡咯并[2,3-b]吡啶-7-甲酰胺
原料
0
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0.0
询
0.0
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202590-98-5 / MFCD02590985
OTX-015
OTX-015
原料
0
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0.0
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0.0
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中华人民共和国
√
933768-63-9 / MFCD033768639
INCB16562 is a novel, selective, and orally bioavailable small-molecule inhibitor of JAK1 and JAK2 markedly selective over JAK3. Treatment of myeloma cells with INCB16562 potently inhibited interleukin-6 (IL-6)-induced phosphorylation of STAT3. INCB16562 abrogated the protective effects of recombinant cytokines or bone marrow stromal cells and sensitized myeloma cells to cell death by exposure to dexamethasone, melphalan, or bortezomib. Oral administration of INCB16562 antagonized the growth of myeloma xenografts in mice and enhanced the antitumor activity of relevant agents in combination studies. INCB16562 is a potent JAK1/2 inhibitor and that mitigation of JAK/STAT signaling by targeting JAK1 and JAK2 will be beneficial in the treatment of myeloma patients, particularly in combination with other agents. ( source: Neoplasia. 2010 Jan;12(1):28-38. ).
原料
0
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0.0
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0.0
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935666-88-9 / MFCD035666889
(S)-5-Chloro-N2-(1-(5-Fluoropyrimidin-2-Yl)Ethyl)-N4-(5-Methyl-1H-Pyrazol-3-Yl)Pyrimidine-2,4-Diamine
(S)-5-氯-N2-(1-(5-氟嘧啶-2-基)乙基)-N4-(5-甲基-1H-吡唑-3-基)嘧啶-2,4-二胺
原料
0
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0.0
询
0.0
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中华人民共和国
√
937272-79-2 / MFCD037272792
PACRITINIB
Pacritinib游离态
原料
0
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0.0
询
0.0
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229305-39-9 / MFCD00057875
Golotimod, also known as Orilotimod, SCV-07, is an orally bioavailable synthetic peptide containing the amino acids D-glutamine and L-tryptophan connected by a gamma-glutamyl linkage with potential immunostimulating, antimicrobial and antineoplastic activities. Although the exact mechanism of action is unknown, golotimod appears to inhibit the expression of STAT-3, reversing immunosuppression and stimulating an anti-tumor immune response. This agent may stimulate the production of T-lymphocytes (in particular the helper T [Th1] cells), activate macrophages, and increase levels of interleukin 2 and interferon gamma. STAT-3, a transcription factor upregulated in many cancer cell types, is involved in tumor cell growth and survival and immunosuppression. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus)
原料
0
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0.0
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0.0
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133550-30-8 / MFCD00209833
(E)-N-Benzyl-2-Cyano-3-(3,4-Dihydroxyphenyl)Acrylamide
(E)-N-苄基-2-氰基-3-(3,4-二羟苯基)丙烯酰胺
原料
0
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0.0
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0.0
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