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T3983TMP195TFMO 2；TMP 195
TMP195 is a selective class IIa histone deacetylase (HDAC) inhibitor.
价 格：￥电议型 号：T3983产 地：中国大陆
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T3973PF-CBP1
PF-CBP1 HCl is a highly selective inhibitor of the bromodomain of CREB-binding protein(CREBBP). It inhibits CREBBP (IC50: 125 nM) and p300 bromodomains (IC50: 363 nM).
价 格：￥电议型 号：T3973产 地：中国大陆
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T3969I-CBP112
I-CBP112 is a specific and potent acetyl-lysine competitive protein-protein interaction inhibitor targeting the CBP/p300 bromodomains.
价 格：￥电议型 号：T3969产 地：中国大陆
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T38648LCecropin P1, porcine acetate
Cecropin P1, porcine acetate is an antibacterial peptide found in Hyalophora cecropia and pig intestine.
价 格：￥电议型 号：T38648L产 地：中国大陆
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T3649BGP-15BGP15；BGP-15 2HCl；BGP 15
BGP-15 is a PARP inhibitor with protecting effect after ischemia-reperfusion injury.
价 格：￥电议型 号：T3649产 地：中国大陆
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T3317SZL P1-41
SZL P1-41, a skp2 inhibitor, can prevent assembly of Skp2-Skp1 complexes. It selectively suppresses Skp2 SCF E3 ligase activity but exhibits no effect on the activity of other SCF complexes. It also inhibits Skp2-mediated p27 and Akt ubiquitination in viv
价 格：￥电议型 号：T3317产 地：中国大陆
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T3217PF-CBP1 hydrochloridePF-CBP1 HCl
PF-CBP1 is a highly selective inhibitor of the bromodomain of CREB-binding protein(CREBBP).It inhibits CREBBP and p300 bromodomains with IC50 of 125 and 363 nM respectively.
价 格：￥电议型 号：T3217产 地：中国大陆
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T2429Olverembatinib dimesylateHQP1351；GZD824 Dimesylate
GZD824 Dimesylate is a novel orally bioavailable Bcr-Abl inhibitor for Bcr-Abl(WT) and Bcr-Abl(T315I).
价 格：￥电议型 号：T2429产 地：中国大陆
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T2415PP121
PP-121 is a multi-targeted inhibitor of PDGFR (IC50: 2 nM), Hck (IC50: 8 nM), mTOR (IC50: 10 nM), VEGFR2(IC50: 12 nM), Src (IC50: 14 nM) and Abl (IC50: 18 nM) , also inhibits DNA-PK (IC50: 60 nM).
价 格：￥电议型 号：T2415产 地：中国大陆
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T2385IpragliflozinASP1941；伊格列净
Ipragliflozin is under investigation in Type 2 Diabetes and Diabetes Mellitus, Type 2.
价 格：￥电议型 号：T2385产 地：中国大陆
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T2156WP1066
WP1066 is a inhibitor of JAK2 (IC50: 2.30 μM) and STAT3 (IC50: 2.43 μM) in HEL cells; shows activity to JAK2, STAT3/5, and ERK1/2, not JAK1 and JAK3. WP1066 has been used in trials studying the treatment of Melanoma, Brain Cancer, Solid Tumors, and Centra
价 格：￥电议型 号：T2156产 地：中国大陆
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T21559OTSSP167 hydrochlorideOTSSP 167 盐酸盐
OTSSP167 hydrochloride is a highly potent inhibitor of MELK(IC50 : 0.41 nM).
价 格：￥电议型 号：T21559产 地：中国大陆
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T21531-NM-PP1PP1 Analog II；1 nM-PP1
1 nM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors.
价 格：￥电议型 号：T2153产 地：中国大陆
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T2045JANEX-1WHI-P131；Jak3 inhibitor I
Janex-1 is a cell-permeable, reversible, effective, ATP-competitive, and selective inhibitor of JAK3 (IC50: 78 μM); little inhibitory against JAK1/2, or Zap/Syk or SRC tyrosine kinases.
价 格：￥电议型 号：T2045产 地：中国大陆
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T2032WHI-P180Janex 3
WHI-P180 is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respectively.
价 格：￥电议型 号：T2032产 地：中国大陆
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T19967FendosalHP 129；HP129；P-71-0129；P71-0129；HP-129；P 71-0129
Fendosal is a non-steroidal anti-inflammatory agent. It is 6.9 to 9.5 times more active than aspirin in the prophylactic and therapeutic adjuvant-induced polyarthritis models of chronic inflammation.
价 格：￥电议型 号：T19967产 地：中国大陆
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T19636MorniflumateMorniflu；UP-164；Niflam；UP 164；UP164；马尼氟酯
Morniflumate is a nonsteroidal anti-inflammatory drug. It is used to treat inflammation.
价 格：￥电议型 号：T19636产 地：中国大陆
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T1932B-AP15NSC 687852
B-AP15(NSC687852) is a selective inhibitor of the deubiquitinating enzymes Usp14 and UCHL5 of the 26S proteasome. It blocks the deubiquitinating activity of the 26S proteasome.
价 格：￥电议型 号：T1932产 地：中国大陆
