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T60220ROS kinases-IN-1；化合物ROS kinases-IN-1ROS kinases-IN-1
ROS kinases-IN-1 is a ROS tyrosine kinase inhibitor with IC50 value of 1.22 μM. ROS kinases-IN-1 shows anti-tumor activity.
价 格：￥电议型 号：T60220产 地：中国大陆
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T60154CDK2-IN-13；化合物 CDK2-IN-13CDK2-IN-13
CDK2-IN-13 is a potent Cyclin-dependent kinase 2 (CDK2) inhibitor (IC50 value: 12 ?M).CDK2-IN-13 is involved in cell cycle regulation and can arrest the cell cycle. CDK2-IN-13 prevents cell division and proliferation, induces apoptosis, and can be used in cancer research.
价 格：￥电议型 号：T60154产 地：中国大陆
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T6014911β-HSD1-IN-11；化合物11β-HSD1-IN-1111β-HSD1-IN-11
11β-HSd1-in-11 is a potent and competitive inhibitor of 11-β-hydroxysteroid dehydrogenase 1 (11β-HSD1) IN rats and humans with IC50 values of 0.34 μM and 0.13 μM, respectively. 11β-Hsvd1-in-11 is a compound used as a chemical compound. 11β-HSD1-IN-11 is a hormone involved in regulating various physiological processes, such as metabolism, inflammation, and stress responses. 11β-Hd1-in-11 is a potential compound for the treatment of metabolic disorders, obesity, and certain inflammatory conditions
价 格：￥电议型 号：T60149产 地：中国大陆
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T60146USP8-IN-1；USP8抑制剂USP8-IN-1
USP8-IN-1 is an inhibitor of USP8 with an IC 50 of 1.9 μM. USP8-IN-1 inhibits H1975 cell growth with a GI 50 of 82.04 μM [1].
价 格：￥电议型 号：T60146产 地：中国大陆
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T60130USP5-IN-1；化合物USP5-IN-1USP5-IN-1
USP5-IN-1 (compound 64) is a potent deubiquitinase USP5 inhibitor, which binds to the USP5 ZnF-UBD with a KD of 2.8 μM and is selective over nine proteins containing structurally similar ZnF-UBD domains. USP5-IN-1 inhibits the USP5 catalytic cleavage of a di-ubiquitin substrate [1].
价 格：￥电议型 号：T60130产 地：中国大陆
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T60105Enpp-1-IN-14；化合物Enpp-1-IN-14Enpp-1-IN-14
Enpp-1-IN-14 is a potent inhibitor of Ectonucleotide Pyrophosphatase/Phosphodiesterase-1 (ENPP1) with an IC50 value of 32.38 nM for recombinant human ENPP-1. Enpp-1-IN-14 has anti-tumor activity.
价 格：￥电议型 号：T60105产 地：中国大陆
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T60077SCP1-IN-1；化合物SCP1-IN-1SCP1-IN-1
SCP1-IN-1 (compound SH T-62) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-1 promotes REST degradation and reduces transcriptional activity. In some glioblastoma cells, the high level of REST protein drives tumor growth. SCP1-IN-1 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity [1].
价 格：￥电议型 号：T60077产 地：中国大陆
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T60039KSQ-4279；化合物KSQ-4279USP1-IN-1；USP1-IN-1
KSQ-4279 (USP1-IN-1) is an inhibitor of USP1 and PARP.KSQ-4279 has anticancer activity and is used in the study of non-small cell lung cancer, osteosarcoma, ovarian, breast, glioblastoma, bladder, uterine and pancreatic cancers.
价 格：￥电议型 号：T60039产 地：中国大陆
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T60029SOS1-IN-11；化合物 SOS1-IN-11SOS1-IN-11
SOS1-IN-11 is an effective inhibitor of SOS1 (IC50 = 30 nM).
价 格：￥电议型 号：T60029产 地：中国大陆
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T60003AC1-IN-1；化合物 AC1-IN-1AC1-IN-1
AC1-IN-1 is a selective inhibitor of adenylyl cyclase type 1 (AC1, IC50 = 0.54 ?M).
价 格：￥电议型 号：T60003产 地：中国大陆
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T5996CB1-IN-1；化合物CB1-IN-1DBPR211；DBPR211|||1-(2,4-二氯苯基)-N-1-哌啶基-4-[[(1-吡咯烷基磺酰基)氨基]甲基]-5-[5-[2-[4-(三氟甲基)苯基
CB1-IN-1 (DBPR211) is a peripherally restricted CB1R antagonist, for CB1R and CB2R with Ki of 0.3 nM and 21 nM,respectively.
价 格：￥电议型 号：T5996产 地：中国大陆
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T5655mAChR-IN-1 hydrochloride；化合物mAChR-IN-1 hydrochloridemAChR-IN-1 hydrochloride
mAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor (mAChR) antagonist, with an IC50 of 17 Nm.
价 格：￥电议型 号：T5655产 地：中国大陆
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T5476mAChr-in-1；化合物mAChr-in-1mAChr-in-1
mAChR-IN-1 is muscarinic cholinergic receptor(mAChR) antagonist (IC50=17 nM).
价 格：￥电议型 号：T5476产 地：中国大陆
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T5466Tyrosine kinase-IN-1；化合物Tyrosine kinase-IN-1Tyrosine kinase-IN-1
Tyrosine kinase-IN-1 is a multi-targeted tyrosine kinase inhibitor（KDR, Flt-1, FGFR1 and PDGFRα with IC50s of 4nM, 20nM, 4nM, 2 nM ,respectively）
价 格：￥电议型 号：T5466产 地：中国大陆
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T5456WNK-IN-11；化合物WNK-IN-11Allosteric WNK Kinase Inhibitor；Allosteric WNK Kinase Inhibitor
WNK-IN-11 (Allosteric WNK Kinase Inhibitor) is an allosteric With-No-Lysine (WNK) kinase inhibitor,WNK1(IC50 : 4 nM)
价 格：￥电议型 号：T5456产 地：中国大陆
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T5411PDE10-IN-1化合物SEP-0372814SEP-0372814
PDE10-IN-1 (SEP-0372814) is used for treating CNS and metabolic disorders.
价 格：￥电议型 号：T5411产 地：中国大陆
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T5401GSK2983559 active metabolite；化合物GSK2983559GSK2983559|||RIPK2 inhibitor 1|||RIPK2-IN-1；GSK2983559|||R
GSK2983559 active metabolite (RIPK2-IN-1) is a potent, selective receptor-interacting protein-2 (RIP2) kinase inhibitor.
价 格：￥电议型 号：T5401产 地：中国大陆
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T5393CK1-IN-1；化合物CK1-IN-1PUN51207；PUN51207
CK1-IN-1 (PUN51207) is a casein kinase 1 (CK1) inhibitor. CK1-IN-1 has IC50s of 15 nM, 16 nM, 73 nM for CK1δ, and CK1ε, p38σ MAPK, respectively.
价 格：￥电议型 号：T5393产 地：中国大陆
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T5184ERK5-IN-1；化合物ERK5-IN-1ERK5-IN-1
ERK5-IN-1 is a potent ERK5 inhibitor (IC50: 87 nM). It also inhibits LRRK2[G2019S] (IC50: 26 nM).
价 格：￥电议型 号：T5184产 地：中国大陆
