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产品数：86101
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T6636RefametinibMEK1,allosteric,RDEA 119,BAY-869766,inhibit,Inhibitor,MAP2K,MEK2,orally,MAPKK,RDEA-119,Mi
Refametinib (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
价 格：￥电议型 号：T6636产 地：中国大陆
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TN71361,7-dimethyl-1H-indole-3-carbaldehyde
1,7-dimethyl-1H-indole-3-carbaldehyde is a marine derived natural products found in Lyngbya majuscula.
价 格：￥电议型 号：TN7136产 地：中国大陆
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T7636Phenprocoumoninhibit,Phenprocoumon,Inhibitor
Phenprocoumon is an antagonist of vitamin K(IC50:1 μM).
价 格：￥电议型 号：T7636产 地：中国大陆
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TN5283L-Cysteine hydrochloride hydrateInhibitor,semi-essential,anorectic,endogenous,1880366,L-Cysteine hyd
L-Cysteine hydrochloride hydrate is a conditionally essential amino acid, which acts as a precursor for biologically active molecules such as hydrogen sulphide (H2S), taurine and glutathione. L-Cysteine hydrochloride hydrate suppresses ghrelin and reduces appetite in rodents and humans.
价 格：￥电议型 号：TN5283产 地：中国大陆
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TN3651CichoriinInhibitor,SARS coronavirus,Cichoriin,SARS-CoV,inhibit
Cichoriin is a photosensitive compound, it could be used as herbal photosensitizing agent in treating benign breast tumor in rats.
价 格：￥电议型 号：TN3651产 地：中国大陆
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T22794G36G36
G36 is a cell-permeable non-steroidal antagonist of GPER. G36 inhibits activation by either 17β-estradiol or the GPER-selective agonist G-1 (IC50 = 112 and 165 nM, respectively). G36 has no detectable binding activity to either ERα or ERβ. G36 blocks the activation of PI3K or calcium mobilization triggered by estrogen through GPER and it suppresses ERK activation by estrogen or G-1 but not by EGF. G-36 can be used in combination with GPER-selective agonists, like G-1, to distinguish the roles of
价 格：￥电议型 号：T22794产 地：中国大陆
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T36851LPeptide5 acetatePeptide5 acetate,Peptide-5 aceate (916977-43-0 Free base)
Peptide5 acetate reduces animal swelling, astrogliosis, and neuronal cell death after spinal cord injury. Peptide5 acetate significantly reduces the degree of spinal cord injury (SCI) in a rodent ex vivo model.
价 格：￥电议型 号：T36851L产 地：中国大陆
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TP1236Etelcalcetide hydrochlorideEtelcalcetide hydrochloride,KAI-4169,AMG416,KAI4169,CaSR,KAI 4169,AMG 416
Etelcalcetide hydrochloride is a synthetic peptide as an allosteric modulator of the calcium (Ca)-sensing receptor (CaSR). Etelcalcetide hydrochloride is effective in lowering parathyroid hormone (PTH) concentrations in patients receiving dialysis with secondary hyperparathyroidism receiving hemodialysis.
价 格：￥电议型 号：TP1236产 地：中国大陆
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T9366PyrazoloadeninePyrazoloadenine
Pyrazoloadenine is the inhibitor of human xanthine oxidase.
价 格：￥电议型 号：T9366产 地：中国大陆
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T63536Dual FAAH/sEH-IN-1
Dual FAAH/sEH-IN-1 is a dual inhibitor of sEH (soluble epoxide hydrolase) (IC50: 9.6 nM) and FAAH (fatty acid amide hydrolase) (IC50: 7 nM) with high affinity and anti-inflammatory activity.
价 格：￥电议型 号：T63536产 地：中国大陆
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T0364LDibucaine hydrochlorideinhibit,Na channels,Na+ channels,Cinchocaine,SChE,BSA-gold,Inhibitor,Sodium C
Dibucaine hydrochloride, a long-acting local amide anestheticsis, is usually used for surface anesthesia.
价 格：￥电议型 号：T0364L产 地：中国大陆
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T7362O-304O 304,AMPK,O-304,inhibit,Inhibitor,AMP-activated protein kinase,O304
O-304 is a pan-activator of AMP-activated protein kinase (AMPK).
价 格：￥电议型 号：T7362产 地：中国大陆
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T9611PF-04802367PF367,PF 367,protein,disease,Alzheimer,PF-04802367,PF-367,Glycogen synthase kinase-3,kina
PF-04802367 is a highly selective GSK-3 inhibitor with an IC50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay. It shows desirable central nervous system (CNS) properties and potency. It is equally effective at inhibition of the two known GSK-3 isoforms (GSK-3α and GSK-3β) with IC50 values of 10.0 and 9.0 nM in mobility shift assays, respectively.
价 格：￥电议型 号：T9611产 地：中国大陆
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T6977SB-366791potential,transient,SB 366791,potent,Transient receptor potential channels,Inhibitor,vanill
SB-366791 is a new and selective cinnamide TRPV1 antagonist.
价 格：￥电议型 号：T6977产 地：中国大陆
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T7361VerucerfontGSK 561679,Verucerfont,Corticotropin-releasing Factor Receptor,Inhibitor,GSK-561679,CRFR,
Verucerfont is an antagonist of corticotropin-releasing factor receptor 1 (CRF1) .
价 格：￥电议型 号：T7361产 地：中国大陆
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TP2365LAcetyl tetrapeptide-9 AcetateAcetyl tetrapeptide9 Acetate,Acetyl tetrapeptide 9 Acetate
Acetyl tetrapeptide-9 Acetate plays a role in the stimulation of basement membrane polysaccharide (lumican) and the synthesis of collagen I.
价 格：￥电议型 号：TP2365L产 地：中国大陆
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T60036ML-SA5MLSA5,ML SA5
ML-SA5 is an MCOLN1 agonist and arrests autophagic flux by perturbing fusion between autophagosomes and lysosomes.
价 格：￥电议型 号：T60036产 地：中国大陆
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T10936D-I03
D-I03 is a selective RAD52 inhibitor with a Kd of 25.8 ?M. D-I03 specifically inhibits RAD52-dependent single-chain annealing (SSA) and D-loop formation, with IC50 of 5 ?M and 8 ?M, respectively. D-I03 inhibited the growth of BRCA1 and BRCA2 deficient cells and inhibited the formation of damage-induced RAD52 foci, but does not effect on RAD51 foci induced by Cisplatin.
价 格：￥电议型 号：T10936产 地：中国大陆
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TP1938LRS09 2TFA (1449566-36-2 free base)RS09 2TFA (1449566362 free base),RS09 2TFA (1449566 36 2 free base
RS09 2TFA is a TLR4 agonist. Promotes NF-κB nuclear translocation and induces inflammatory cytokine secretion in RAW264.7 macrophages in vitro. It acts as an adjuvant in vivo and enhances X-15 specific antibody serum concentrations.
价 格：￥电议型 号：TP1938L产 地：中国大陆
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T60064WAY-270360WAY270360,WAY 270360
WAY-270360 is a sirtuin modulator and an epidermal growth factor receptor (EGFR) inhibitor.
价 格：￥电议型 号：T60064产 地：中国大陆
