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产品数：86101
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T7096TildipirosinTildipirosin,Antibiotic,Inhibitor,inhibit,Bacterial
Tildipirosin is a 16-membered macrolide used as an antibiotic in veterinary medicine. Like other macrolides, it inhibits protein synthesis in bacteria and blocks the production of biofilms.
价 格：￥电议型 号：T7096产 地：中国大陆
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T60196IHMT-PI3Kδ-372 S-isomerIHMTPI3Kδ372Sisomer
IHMT-PI3Kδ-372 S-isomer is a potent and selective PI3Kδ inhibitor with an IC50 of 14 nM. IHMT-PI3Kδ-372 S-isomer shows high selectivity over other class I PI3Ks (56?83 fold) and other protein kinases. IHMT-PI3Kδ-372 can be uesd for chronic obstructive pulmonary disease (COPD) research.
价 格：￥电议型 号：T60196产 地：中国大陆
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T12238NNC 55-0396NNC 55-0396,inhibit,Ca2+ channels,Inhibitor,NNC 550396,NNC 55 0396,Calcium Channel,Ca cha
NNC 55-0396 is a highly selective blocker of T-type calcium channel with IC50 of 6.8 μM. NNC 55-0396 can be used in studies about preventing human ovarian cancer cell proliferation.
价 格：￥电议型 号：T12238产 地：中国大陆
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T19966Clemastine
Clemastine is an antagonist of the H1 receptor and exhibits anti-inflammatory effects.
价 格：￥电议型 号：T19966产 地：中国大陆
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T9967MAGL-IN-5Inhibitor,inhibit,MAGLIN5,MAGL IN 5,FAAH,Fatty acid amide hydrolase,Monoacylglycerol lipase
MAGL-IN-5 is a non-selective lipase inhibitor.
价 格：￥电议型 号：T9967产 地：中国大陆
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T9605Sangivamycincells,Nucleoside Antimetabolite/Analog,Sangivamycin,antitumor,NSC-65346,PKC,MCF7,NSC6534
Sangivamycin is an effective inhibitor of protein kinase C (PKC, Ki = 10 μM). Sangivamycin exhibits antiproliferative activity against a variety of human cancers.
价 格：￥电议型 号：T9605产 地：中国大陆
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T9648SIRT1-IN-1inhibit,Cytomegalovirus,CMV,antiviral,indole,Inhibitor,Sirtuin,SIRT1IN1,SIRT1 IN 1
SIRT1-IN-1 is a selective inhibitor of SIRT1 with an IC50 of 205 nM. SIRT1-IN-1 is an inhibitor of cytomegalovirus (CMV) with antiviral activity.
价 格：￥电议型 号：T9648产 地：中国大陆
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T9680IrloxacinInhibitor,acid pH,antibacterial agent,Bacterial,gram-positive,oral,Irloxacin,Pirfloxacin,gr
Irloxacin is a new quinolone derivative, and shows greater activity with an acid pH. Irloxacin has a good in vitro antimicrobial spectrum against both gram-positive and gram-negative bacteria.
价 格：￥电议型 号：T9680产 地：中国大陆
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T7205A-967079TRP Channel,inhibit,Transient receptor potential channels,A 967079,Inhibitor,A-967079,A96707
A 967079 is a potent, selective, and bioavailable inhibitor of the TRPA1 channel, with IC50 values of 67 and 289 nM for the human and rat isoforms, respectively.
价 格：￥电议型 号：T7205产 地：中国大陆
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T9638CCT241161CCT241161
CCT241161 is an orally active pan- RAF inhibitor with IC 50 s of 3, 6, 10, 15 and 30 nM for LCK, CRAF, SRC, V600E-BRAF and BRAF, respectively. CCT241161 shows good activity to in BRAF and NRAS mutant melanomas. CCT241161 also shows anticancer cell proliferative activity [1].
价 格：￥电议型 号：T9638产 地：中国大陆
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T8745Compound 23Inhibitor,Raf,A375,HT-29,Compound 23,inhibit,BRAF-V600E,ubiquitin-proteasome system,antic
Compound 23 selectively induces degradation of BRAF-V600E but not wildtype BRAF.
价 格：￥电议型 号：T8745产 地：中国大陆
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T11961MBM-55SMBM 55S,MBM55S
MBM-55S is an effective inhibitor of Nek2 with an IC50 of 1 nM. MBM-55S indecus cell cycle arrest and apoptosis thereby inhibiting the proliferation of cancer cells. MBM-55S shows antitumor activities.
价 格：￥电议型 号：T11961产 地：中国大陆
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T16557PNU-159682inhibit,non-Hodgkin’s lymphoma,PNU159682,ADCs Toxin,PNU-159682,acute myeloid leukemia,ADC
PNU-159682 is a highly effective metabolite of the anthracycline nemorubicin. PNU-159682 has outstanding cytotoxicity. PNU-159682 is an effective ADCs cytotoxin.
价 格：￥电议型 号：T16557产 地：中国大陆
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T9692PaltusotinePaltusotine,Somatostatin Receptor,CRN-00808,CRN 00808,Inhibitor,IGF-1,orally,CRN00808,SST
Paltusotine is a nonpeptide, small molecule somatostatin type 2 (SST2) receptor agonist with high oral bioavailability. Paltusotine maintains GH and IGF-1 levels in acromegaly patients
价 格：￥电议型 号：T9692产 地：中国大陆
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T6366A-9664922-[2-氟-4-[(2S)-2-吡咯烷基]苯基]-1H-苯并咪唑-7-甲酰胺；A966492；A 966492
A-96649 is a new-type and effective inhibitor. The Ki of A-966492 for PARP1 and PARP2 is 1 nM and 1.5 nM, respectively.
价 格：￥电议型 号：T6366产 地：中国大陆
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T6310GW3965 hydrochlorideGW3965 HCl
GW3965 HCl is an effective and specific LXR agonist for hLXRα/β (EC50: 190/30 nM).
价 格：￥电议型 号：T6310产 地：中国大陆
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T6309AZ960AZ 960
AZ 960 is an effective ATP competitive JAK2 inhibitor (IC50/Ki: <3 nM and0.45 nM).
价 格：￥电议型 号：T6309产 地：中国大陆
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T6296RAF265CHIR-265
RAF265 (CHIR-265) is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 nM, and exhibits potent inhibition on VEGFR2 phosphorylation with EC50 of 30 nM. Phase 2.
价 格：￥电议型 号：T6296产 地：中国大陆
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T6277DoramapimodBIRB 796；达马莫德；度马莫德
Doramapimod is a highly potent inhibitor of p38 MAPK (Kd: 0.1 nM), but weakly inhibits c-RAF, Fyn, Lck, ERK-1, SYK, IKK2, and ZAP-70.
价 格：￥电议型 号：T6277产 地：中国大陆
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T6196PP1EI 275；AGL 1872
PP1, a specific and effective Src inhibitor, is with IC50 for Lck/Fyn is 5 nM/ 6 nM, respectively.
价 格：￥电议型 号：T6196产 地：中国大陆
