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T6674L-Ascorbic acid sodium saltCa channels,Vitamin C,Reactive Oxygen Species,L Ascorbic acid sodium salt
Sodium Ascorbate is a more bioavailable form of vitamin C that is an alternative to taking ascorbic acid as a supplement.
价 格：￥电议型 号：T6674产 地：中国大陆
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T60054EJMC-1
EJMC-1 is an inhibitor of TNF-α with an IC50 value of 42 μM and can be used in studies about auto-inflammatory diseases.
价 格：￥电议型 号：T60054产 地：中国大陆
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T73513-Methylcytidineinhibit,3-Methylcytidine,Inhibitor,3Methylcytidine,Nucleoside Antimetabolite/Analog,
3-Methylcytidine as biomarkers of four different types of cancer: lung cancer, gastric cancer, colon cancer, and breast cancer.
价 格：￥电议型 号：T7351产 地：中国大陆
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T25192Butyrolactone I
Butyrolactone I is an ATP-competitive inhibitor of CDK and cdc2 kinase family. Butyrolactone I shows antitumor effects in non-small cell lung, small cell lung, and prostate cancer cell lines.
价 格：￥电议型 号：T25192产 地：中国大陆
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T9121AG-636inhibit,oral,AG 636,AG-636,reversible,DHODH,anticancer,AG636,Inhibitor,Dihydroorotate Dehydrog
AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.
价 格：￥电议型 号：T9121产 地：中国大陆
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T8144Raffinoseshort-chain,inhibit,Raffinose,trisaccharide,Inhibitor,Endogenous Metabolite,oligosaccharide
Raffinose is a natural compound.
价 格：￥电议型 号：T8144产 地：中国大陆
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T37445EtanerceptEtanercept
Etanercept, a dimeric fusion protein that binds TNF, acts as a TNF inhibitor. Etanercept competitively inhibits the binding of both TNF-α and TNF-β to cell surface TNF receptors, rendering TNF biologically inactive. Etanercept shows efficacy against rheumatoid arthritis, juvenile idiopathic arthritis, and plaque psoriasis.
价 格：￥电议型 号：T37445产 地：中国大陆
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T9400KCNQ2/3 activator-1KCNQ2/3 activator-1,activator,Potassium Channel,KCNQ2/3,KCNQ2/3 activator 1,KcsA,
N-[4-(6-Fluoro-3,4-dihydro-2(1H)-isoquinolinyl)-2,6-dimethylphenyl]-3,3-dimethylbutanamide is a chemical compound.
价 格：￥电议型 号：T9400产 地：中国大陆
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T8507MAC-545496Bacterial,S. aureus,Antivirulence,Inhibitor,MAC545496,mprF,nanomolar,GraR,MAC-545496,MRSA,
MAC-545496 is a glycopeptide-resistance-associated protein R (GraR) inhibitor, is an antivirulence agent.
价 格：￥电议型 号：T8507产 地：中国大陆
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T10852CNS-5161 hydrochloride
CNS-5161 hydrochloride is a new antagonist of NMDA ion-channel. It interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate.
价 格：￥电议型 号：T10852产 地：中国大陆
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TN6963HentriacontaneHentriacontane
Hentriacontane is a natural product with various pharmacological effects including anti-inflammatory, antitumor, and antimicrobial activities.
价 格：￥电议型 号：TN6963产 地：中国大陆
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T7978CyclopentadecanoneCyclopentadecanone
Cyclopentadecanone Used in perfumery (musk odour).
价 格：￥电议型 号：T7978产 地：中国大陆
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T7222GS-441524GS-441524,Inhibitor,feline,SARS coronavirus,virus,FIPV,infectious,peritonitis,DNA/RNA Synth
GS-441524 treatment of cats with naturally occurring feline infectious peritonitis.
价 格：￥电议型 号：T7222产 地：中国大陆
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T7949NCC007inhibit,NCC-007,Inhibitor,NCC007,NCC 007,Casein Kinase
NCC007 is a novel CKIα and CKIδ dual inhibitors by structural modification of N9 and C2 position of longdaysin.
价 格：￥电议型 号：T7949产 地：中国大陆
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T9767CC618CC618,CC-618
CC618 is a selective PPARβ/δ antagonist with an IC50 of 10.0 μM.
价 格：￥电议型 号：T9767产 地：中国大陆
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T7679UBCS039Autophagy,UBCS039,UBCS 039,inhibit,Sirtuin,Inhibitor,UBCS-039
UBCS039 is the first synthetic Sirt6 activator(EC50 : 38 μM)
价 格：￥电议型 号：T7679产 地：中国大陆
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T8950CAY10698CAY-10698,LOX,CAY10698,inhibit,CAY 10698,Inhibitor,12-Lipoxygenase,Lipoxygenase
CAY10698 is a 12-lipoxygenase inhibitor (12-LO; IC50 of 5.1 μM).
价 格：￥电议型 号：T8950产 地：中国大陆
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T0136CiticolineInhibitor,Endogenous Metabolite,inhibit,Citicoline,Apoptosis
Citicoline is an intermediate in the synthesis of phosphatidylcholine, a component of cell membranes. Citicoline exerts neuroprotective effects.
价 格：￥电议型 号：T0136产 地：中国大陆
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TP1049LOrnipressin Acetate（3397-23-7，free）Ornipressin Acetate（3397 23 7，free）,Ornipressin Acetate（3397237，f
Ornipressin Acetate is a potent vasoconstrictor, hemostatic and renal agent.
价 格：￥电议型 号：TP1049L产 地：中国大陆
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PDK0269Compound PDK0269Compound PDK0269
PBG (1-Phenylbiguanide HCl), as 5-HT3 receptor agonists(3–100 μM, pEC50 5.05±0.06), acutely increased XII (hypoglossal) burst frequency and regularity, and decreased bursts/episode . Phenylbiguanide produced a dose-related (10-500 microM) increase in the release of dopamine (280-2000%). When nomifensine (5 microM) was included in the Ringer solution, the effect of PBG on the release of dopamine was ameliorated or inhibited. Phenylbiguanide, infused intravenously for 15 min, elicited a sustained
价 格：￥电议型 号：PDK0269产 地：中国大陆
