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T8960MONNACl-Channels,inhibit,MONNA,Inhibitor,Chloride Channel
MONNA is a potent TMEM16A (Anoctamin-1) blocker (IC50 : 80 nM). It induces vasorelaxation of rodent resistance arteries in presence or absence of chloride ions.
价 格：￥电议型 号：T8960产 地：中国大陆
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T962810074-A4Inhibitor,10074-A4,10074-A-4,anticancer,cycle,CDK4,inhibit,cell,c-Myc,10074A4,Myc,CCND2,1007
10074-A4 is a c-Myc binding compound that associates with c-Myc370–409 and behaves like a “ligand cloud” around a “protein cloud”, with distinct features from that of a non-binding ligand.
价 格：￥电议型 号：T9628产 地：中国大陆
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T9180LUF6096
LUF6096 is a potent allosteric enhancer of the adenosine A3 receptor. LUF6096 is able to allosterically enhance agonist binding. LUF6096 shows low orthosteric affinity for any of the adenosine receptors. LUF6096 shows protective effects in myocardial ischemia/reperfusion injury.
价 格：￥电议型 号：T9180产 地：中国大陆
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T9691L(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate(D Trp12,Tyr34) pTH (7 34) amide (bovine) acetate,(
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate is a highly potent antagonist of parathyroid hormone (PTH) The Ki value is 69 nM in bovine renal cortical membrane.
价 格：￥电议型 号：T9691L产 地：中国大陆
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T6S1966CurculigosideCurculigoside,Janus kinase,NF-κB,JAK,Nuclear factor-κB,Nuclear factor-kappaB,STAT,inhib
1. Curculigoside can prevent bone loss , improve osteogenesis and inhibit osteoclastogenesis of hAFSCs, suggesting its potential use to regulate hAFSC osteogenic differentiation for treating bone disorders. 2. Curculigoside can promote calcium deposition and increase the levels of ALP and Runx2 in osteoblasts under oxidative stress via anti-oxidative character. 3. Curculigoside possesses potent antioxidant properties against oxidative stress insults. can protect endothelial cells against oxidati
价 格：￥电议型 号：T6S1966产 地：中国大陆
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T8962TM5007TM 5007,inhibit,TM5007,PAI-1,Plasminogen activator inhibitor-1,Inhibitor,TM-5007
TM5007 is a poent inhibitor of plasminogen activator inhibitor-1 (PAI-1; IC50 of 29 uM).
价 格：￥电议型 号：T8962产 地：中国大陆
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TP1348FC131 TFA (606968-52-9 free base)FC131 TFA (606968529 free base),FC131 TFA (606968 52 9 free base),F
FC131 TFA is an antagonist of CXCR4 that inhibits the binding of [125I] -sdf-1 to CXCR4(IC50 : 4.5 nM ), and has anti-hiv activity.
价 格：￥电议型 号：TP1348产 地：中国大陆
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T9612Antibacterial agent 27?Inhibitor,Candida,antibacterial,Antibacterial agent27,Antibacterial agent 27?
Antibacterial agent 27 has potent anti-Candida activity.
价 格：￥电议型 号：T9612产 地：中国大陆
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T22964Glemanserin
Glemanserin is a specific 5-HT2A antagonist with Ki values of 0.54 nM, 2.5 nM and 2.89 nM for rabbit, human and rat 5-HT2A.
价 格：￥电议型 号：T22964产 地：中国大陆
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T9996NCT-58
NCT-58 is a potent C-terminal HSP90 inhibitor. NCT-58 does not induce the heat shock response (HSR). NCT-58 elicits anti-tumor activity via the simultaneous downregulation of HER family members as well as inhibition of Akt phosphorylation. NCT-58 kills Trastuzumab-resistant breast cancer stem-like cells. NCT-58 induces apoptosis in HER2-positive breast cancer cells.
价 格：￥电议型 号：T9996产 地：中国大陆
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TN1596DL-TyrosineDLTyrosine,meat,DL Tyrosine,animal,inhibit,DL-Tyrosine,nervous,acid,Inhibitor,amino,precu
DL-Tyrosine is a natural product.
价 格：￥电议型 号：TN1596产 地：中国大陆
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T6928Pantoprazolerelease,exosome,orally,Doxorubicin,Autophagy,SKF 96022,Inhibitor,A431,BY-1023,H+/K+-ATPa
Pantoprazole is a proton pump inhibitor used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
价 格：￥电议型 号：T6928产 地：中国大陆
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T36964BML-259BML-259,protein,p53,CDK,death,disease,neurotoxicity,cell,Inhibitor,inhibit,Cyclin dependent k
BML-259 is an inhibitor of CDK5 and CDK2 with IC50s of 64 and 98 nM, respectively. BML-259 can be used in studies about the treatment of cancer and neurodegenerative diseases.
价 格：￥电议型 号：T36964产 地：中国大陆
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TN24961,4-Anthraquinone1,4Anthraquinone,1,4 Anthraquinone
1,4-Anthraquinone is an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro.1,4-Anthraquinone is proposed as a novel pre-column reagent for high performance liquid chromatography (HPLC) determination of N-acetylcysteine (NAC) and captopril (CAP) in pharmaceutical formulations.
价 格：￥电议型 号：TN2496产 地：中国大陆
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TQ0196Cucurbitacin IJanus kinase,JAK,NSC521777,Inhibitor,JSI 124,JSI124,Cucurbitacin I,STAT,NSC 521777,inh
Cucurbitacin I, a natural compound, is a selective inhibitor of JAK2/STAT3 with anti-cancer activity.
价 格：￥电议型 号：TQ0196产 地：中国大陆
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T8096Diethyl succinateDiethyl Butanedioate,inhibit,Diethyl,Inhibitor,Diethyl succinate
Diethyl succinate is the diethyl ester of succinate and acts as an irritant.
价 格：￥电议型 号：T8096产 地：中国大陆
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T16960SultiameInhibitor,Carbonate dehydratase,Carbonic Anhydrase,Sultiame,inhibit
Sultiame is an inhibitor of carbonic anhydrase. Sultiame can be used in antiepileptic research.
价 格：￥电议型 号：T16960产 地：中国大陆
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TN1965N-?BenzyllinolenamideFatty acid amide hydrolase,Autophagy,N ?Benzyllinolenamide,inhibit,Inhibitor,N-
N-Benzyllinolenamide is a natural product. It is an inhibitor of fatty acid amide hydrolase (FAAH, IC50 of 41.8 μM).
价 格：￥电议型 号：TN1965产 地：中国大陆
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TQ0111LDN-192960DYRK,Dual specificity tyrosine regulated kinase,Inhibitor,Dual specificity tyrosine phosph
LDN-192960 is a potent inhibitor of Haspin and DYRK2 (IC50s: 10 nM and 48 nM).
价 格：￥电议型 号：TQ0111产 地：中国大陆
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T9694EmraclidineEmraclidine,muscarinic,Schizophrenia,Parkinson,Muscarinic acetylcholine receptor,CVL231,I
Emraclidine is a muscarinic M4 receptor positive allosteric modulator and can be used in neurological diseases studies.
价 格：￥电议型 号：T9694产 地：中国大陆
