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T15368LGalantide acetate
Galantide acetate, a non-specific galanin receptor antagonist, is a peptide consisting of fragments of galanin and substance P. Galantide acetate recognizes two classes of galanin binding sites (KD<0.1 nM and ~6 nM) in the rat hypothalamus. Galantide acetate dose dependently (IC50=1.0 nM) antagonizes the galanin-mediated inhibition of the glucose-induced insulin secretion from mouse pancreatic islets. Galantide acetate appears to bind to a single population of SP receptors (KD~40 nM).
价 格：￥电议型 号：T15368L产 地：中国大陆
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T17252WAY-204688
WAY-204688 is a selective and orally active estrogen receptor inhibitor of NF-κB transcriptional activity (IC50 = 122 nM in HAECT-1 cells).
价 格：￥电议型 号：T17252产 地：中国大陆
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T7687AC 45594AC 45594
AC 45594 is an agonist of steroidogenic factor 1 (SF-1) ( IC50 : 50-100 nM)
价 格：￥电议型 号：T7687产 地：中国大陆
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T8645PF-06446846Threonine proteases,PF06446846,Inhibitor,80S ribosome,Selective,PF 06446846,Ser/Thr Prote
PF 06446846 is a potent and selective PCSK9 inhibitor
价 格：￥电议型 号：T8645产 地：中国大陆
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T6468D-glutamineMitophagy,inhibit,Autophagy,D glutamine,Dglutamine,D-Glutamine,Endogenous Metabolite,Mito
D-glutamine, an D type stereoisomer of glutamine, is one of the 20 amino acids which is encoded by the standard genetic code.
价 格：￥电议型 号：T6468产 地：中国大陆
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T8368Geranylacetone(Z/E)Geranylacetone(Z/E)
Dihydropseudoionone is a chemical compound.
价 格：￥电议型 号：T8368产 地：中国大陆
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T10682LCARM1-IN-1
CARM1-IN-1 is a selective inhibitor of CARM1 with IC50 of 8.6 μM. CARM1-IN-1 shows weak activity against PRMT1 and SET7 with IC50 > 600 μM.
价 格：￥电议型 号：T10682L产 地：中国大陆
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TMO2681XanthosineEndogenous Metabolite,Xanthosine,inhibit,Inhibitor
Inhibition of inosine and alanine-induced germination of Bacillus anthracis Sterne spore pre-incubated for 15 mins.
价 格：￥电议型 号：TMO2681产 地：中国大陆
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T6873Lauric AcidInhibitor,Bacterial,Lauric Acid,Endogenous Metabolite,inhibit
Lauric Acid,which is found naturally in various plant and animal fats and oils, is a saturated medium-chain fatty acid with a 12-carbon backbone. It is a major component of coconut oil and palm kernel oil.
价 格：￥电议型 号：T6873产 地：中国大陆
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T6849UprosertibGSK-2141795,GSK 2141795,Uprosertib,inhibit,Akt,Inhibitor,PKB,Protein kinase B
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailable Akt inhibitor with IC50 of 180 nM, 328 nM, and 38 nM for Akt 1, 2 and 3, respectively. Phase 2.
价 格：￥电议型 号：T6849产 地：中国大陆
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T6824EAI045Inhibitor,Epidermal growth factor receptor,ErbB-1,EGFR,EAI-045,EAI 045,inhibit,HER1,EAI045
EAI045, an allosteric inhibitor, targets towards drug-resistant EGFR mutants but avoids the wild-type receptor.
价 格：￥电议型 号：T6824产 地：中国大陆
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T6680StaurosporineAntibiotic AM2282,Antibiotic,Apoptosis,PKC,Antibiotic AM 2282,AM2282,Protein kinase A,B
Staurosporine is a potent PKC inhibitor for PKCα/γ/η (IC50: 2/5/4 nM), less potent to PKCε (73 nM), PKCδ (20 nM) and little action to PKCζ (1086 nM).
价 格：￥电议型 号：T6680产 地：中国大陆
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T7530PD146176inhibit,tau,brain,triple,NSC-168807,PD146176,Autophagy,pathology,amyloidosis,transgenic,reti
PD146176 is an inhibitor of 15-Lipoxygenase (15-LO) , it inhibits rabbit reticulocyte 15-LO with Ki of 197 nM and IC50 of 0.54 μM. PD146176 reverses cognitive impairment, brain amyloidosis, and tau pathology by stimulating autophagy in aged triple transgenic mice.
价 格：￥电议型 号：T7530产 地：中国大陆
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T26852BMS-605541
BMS-605541 is a potent and selective inhibitor of vascular endothelial growth factor receptor-2 (VEGFR-2) kinase activity(Ki=49 nM).
价 格：￥电议型 号：T26852产 地：中国大陆
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T12809(S)-PF-06873600(S)PF06873600,(S) PF 06873600
(S)-PF-06873600 is the S enantiomer of PF-06873600 which is an inhibitor of CDK.
价 格：￥电议型 号：T12809产 地：中国大陆
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T6892Niraparib tosylatePARP,Niraparib tosylate,Apoptosis,inhibit,bioavailable,MK-4827,MK4827,cancer,damag
MK-4827(Niraparib) tosylate (with IC50 of 3.8 nM/2.1 nM) is a selective PARP1/PARP2 inhibitor.
价 格：￥电议型 号：T6892产 地：中国大陆
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T8493IngliforibInhibitor,GPi296,GPi-296,CP368296,CP-368296,Ingliforib,inhibit
Ingliforib is a novel glycogen phosphorylase inhibitor,has antihyperglycemic and cardioprotective properties.
价 格：￥电议型 号：T8493产 地：中国大陆
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T8463PF-06873600PF06873600,PF 06873600
PF-06873600 is a selective and orally bioavailable cyclin-dependent kinase (CDK) inhibitor(CDK2, CDK4 and CDK6 with Ki of 0.09 nM, 0.13 nM and 0.16 nM, respectively), has potential antineoplastic activity.
价 格：￥电议型 号：T8463产 地：中国大陆
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T16868SEC inhibitor KL-2
SEC inhibitor KL-2 (KL-2) is a potent, selective super elongation complex (SEC) inhibitor. SEC inhibitor KL-2 exhibits a dose-dependent inhibitory effect on AFF4-CCNT1 interaction (Ki: 1.50 μM).
价 格：￥电议型 号：T16868产 地：中国大陆
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T7675Substance P (1-7) 2TFA(68060-49-1(free base))Substance P (1 7) 2TFA(68060 49 1(free base)),Substance
Substance P (1-7) 2TFA(68060-49-1(free base)) is the major bioactive metabolite formed after proteolytic degradation of the tachykinin substance P (SP),with anti-inflammatory, anti-nociceptive and anti-hyperalgesic effects
价 格：￥电议型 号：T7675产 地：中国大陆
