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T6781BenzenesulfonamideInhibitor,inhibit,QSAR study,Benzenesulfonamide,carbonic anhydrases,Carbonic Anhyd
Benzenesulfonamide ia an inhibitor of carbonic anhydrases.
价 格：￥电议型 号：T6781产 地：中国大陆
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T7839Lasofoxifene Tartrateosteoporosis,inhibit,Estrogen Receptor/ERR,arthritis,CP 336156,endocrine resist
Lasofoxifene Tartrate is a third-generation, non-steroidal selective estrogen receptor modulator.
价 格：￥电议型 号：T7839产 地：中国大陆
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TP1433CMD178 TFACMD178 TFA,CMD-178 TFA
CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.
价 格：￥电议型 号：TP1433产 地：中国大陆
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TN6785DihydrocatalpolDihydrocatalpol
Dihydrocatalpol,a natural product obtained from the herbs of Rehmannia glutinosa.
价 格：￥电议型 号：TN6785产 地：中国大陆
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T9878CroconazoleCROCONAZOLE
Croconazole exhibited dose-dependent inhibitory activity on the 5-lipoxygenase (5-LOX) of neutrophils. Croconazole is an antimycotic agent. The IC50s for the synthesis of leukotriene B4 (LTB4) and 5-hydroxyeicosatetraenoic acid (5-HETE) is 7.8 +/- 1.7 and
价 格：￥电议型 号：T9878产 地：中国大陆
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T7476AS057278Prepulse inhibition,Inhibitor,Non-peptidic,D-amino acid oxidase,AS 057278,inhibit,Schizophre
AS057278 is an D-amino acid oxidase (DAAO) inhibitor.
价 格：￥电议型 号：T7476产 地：中国大陆
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T7862VU6015929VU6015929,VU-6015929
VU6015929 is an inhibitor of active dual discoidin domain receptor 1/2 (DDR1/2)( IC50s of 4.67 nM and 7.39 nM, respectively).
价 格：￥电议型 号：T7862产 地：中国大陆
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T7833TLX agonist 1TLX agonist-1,transcriptional,TLX agonist 1,repressive,Inhibitor,ligand,inhibit,TLX ago
TLX agonist 1 is an orphan nuclear receptor tailless (TLX, NR2E1) modulator
价 格：￥电议型 号：T7833产 地：中国大陆
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T9678ML328ML328,ML-328
ML328 is a potent and selective inhibitor of bacterial AddAB(IC50 = 1.0 μM) and RecBCD(IC50 = 4.8 μM) helicase-nucleases.
价 格：￥电议型 号：T9678产 地：中国大陆
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T1782LCanagliflozin hemihydrate
Canagliflozin hemihydrate is a drug of the gliflozin class or subtype 2 sodium-glucose transport inhibitors used for the treatment of type 2 diabetes. SGLT2 is responsible for at least 90% of renal glucose reabsorption (SGLT1 being responsible for the remaining 10%). Blocking this transporter causes up to 119 grams of blood glucose per day to be eliminated through the urine, corresponding to 476 kilocalories.
价 格：￥电议型 号：T1782L产 地：中国大陆
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T7846Aegelineαsyn,Aegeline,yeast,Inhibitor,protein,Sec22p,inhibit,toxicity,Fungal,SNARE
Aegeline is an alkaloidal-amide, isolated from the leaves of Aegle marmelos and have shown antihyperglycemic as well as antidyslipidemic activities in the validated animal models of type 2 diabetes mellitus.
价 格：￥电议型 号：T7846产 地：中国大陆
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T8478SC-43antiproliferative,Inhibitor,SC-43,SHP-1,PTPN6,Phosphatase,Apoptosis,caspase-3,SC 43,anti-fibrot
SC-43 is a potent and orally active agonist of SHP-1 (PTPN6). SC-43 inhibits the phosphorylation of STAT3 and induces cell apoptosis, and with anti-fibrotic and anticancer effects.
价 格：￥电议型 号：T8478产 地：中国大陆
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T6S0078Oxypeucedanin hydrateInhibitor,inhibit,Oxypeucedanin,(+)-Oxypeucedanin,Oxypeucedanin hydrate,D. anet
1. Oxypeucedanin hydrate has antioxidant activity. 2. Oxypeucedanin hydrate is an antimutagenic agent. 3. Oxypeucedanin hydrate exhibits carbohydrate metabolizing enzymes inhibitory effect.
价 格：￥电议型 号：T6S0078产 地：中国大陆
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T6778BDA-366Inhibitor,BDA-366,Antitumor,Bcl-2 Family,inhibit,Bcl2-BH4 domain,Anticancer,BDA 366,Antiapopt
BDA-366 is a potent Bcl2 antagonist, binding Bcl2-BH4 domain with high affinity and selectivity (Ki = 3.3 nM). BDA-366 induces conformational change in Bcl2 that abrogates its antiapoptotic function, converting it from a survival molecule to a cell death inducer. BDA-366 suppresses growth of lung cancer cells[1].
价 格：￥电议型 号：T6778产 地：中国大陆
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T8678NaphthazarinNaturally,Apoptosis,Naphthazarin,stress,microtubules,mitochondrial,AIF,Inhibitor,p21,lys
Naphthazarin is effective by various cellular mechanisms including oxidative stress, activation of mitochondrial apoptosis-inducing factor (AIF), depolymerization of microtubules, interference with lysosomal function and p53-dependent p21 activation. It triggers apoptosis and has anti-tumor effects
价 格：￥电议型 号：T8678产 地：中国大陆
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T67886Girard’s Reagent T
Girard´s Reagent T is a biochemical reagent. Girard´s Reagent T under mild acid or alkaline conditions, reacts with aldehydes and ketones containing α-dicarbonyl functional groups to produce addition compounds which strongly absorb ultraviolet light.
价 格：￥电议型 号：T67886产 地：中国大陆
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T10783CGS 15435CGS 15435
CGS 15435 is a potent inhibitor of thromboxane (TxA2) synthetase (IC50: 1 nM). It has a selectivity for Tx synthetase 100000-fold greater than that for PGI2 synthetase, cyclooxygenase, and lipoxygenase enzymes.
价 格：￥电议型 号：T10783产 地：中国大陆
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T978520-(tert-Butoxy)-20-oxoicosanoic acid20 (tert Butoxy) 20 oxoicosanoic acid,Inhibitor,inhibit,ADC Lin
20-(tert-Butoxy)-20-oxoicosanoic acid is a alkyl-chain-based PROTAC linker. 20-(tert-Butoxy)-20-oxoicosanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9785产 地：中国大陆
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T7778LGlypromate acetate(32302-76-4 free base)Glypromate acetate(32302 76 4 free base),Glypromate acetate(
Glypromate acetate is a neuroprotective agent, is a weak NMDA receptor agonist.
价 格：￥电议型 号：T7778L产 地：中国大陆
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T7946AER-271Inhibitor,AER-271,AQP4,AER-270,stroke,inhibit,aquaporin-4,injury,AER 271,acute,AER271,CNS,isc
AER-271 is an inhibitor of aquaporin-4.
价 格：￥电议型 号：T7946产 地：中国大陆
