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T7806Licarbazepinepartial,Licarbazepine,Sodium Channel,Na channels,voltage,Inhibitor,sodium,seizures,stab
Licarbazepine is the pharmacologically active metabolite of oxcarbazepine, a drug indicated for the treatment of partial seizures and bipolar disorders.
价 格：￥电议型 号：T7806产 地：中国大陆
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TCS2070Homogentisic acidHomogentisic acid,inhibit,Endogenous Metabolite,Inhibitor
1. Homogentisic acid shows interesting antioxidant and antiradical activities, and protective effect against thermal-cholesterol degradation, comparable to those of well known antioxidants. 2. Homogentisic acid is the primary precursor of melanin synthesis in Vibrio cholerae, a Hyphomonas strain, and Shewanella colwelliana. 3. A derivative of homogentisic acid which inhibits Pfnek-1 with an IC(5) around 1.8 muM, this product is moderately active in vitro against a FcB1 P. falciparum strain (IC(5
价 格：￥电议型 号：TCS2070产 地：中国大陆
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T9045BemotrizinolBemotrizinol,inhibit,atomic oxygen,Tinosorb S,Inhibitor,feasible acceptor
Bemotrizinol is a UVA absorber used as a topical sunscreen.
价 格：￥电议型 号：T9045产 地：中国大陆
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TN1962Myricetin 3-O-galactosideMyricetin 3 O galactoside,Myricetin 3Ogalactoside
Myricetin 3-O-galactoside has cytotoxicity, antioxidant, anti-genotoxic, antinociceptive and anti-inflammatory effects, the effects are related to peripheral inhibition of nitric oxide synthesis, mainly inducible nitric oxide synthase (iNOS).
价 格：￥电议型 号：TN1962产 地：中国大陆
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T9430Venadaparibinhibit,PARP,Venadaparib,IDX1197,Inhibitor,solid,IDX 1197,tumors,anticancer,poly ADP ribo
Venadaparib (IDX-1197) is a potent, selective and orally active PARP inhibitor with IC50s of 1.4 nM and 1.0 nM for PARP1 and PARP2, respectively. Venadaparib is insensitive to PARP-5. Venadaparib prevents the repair of DNA single-strand breaks (SSBs) and can be used in solid tumor research.
价 格：￥电议型 号：T9430产 地：中国大陆
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T6828ZL0420inhibit,Epigenetic Reader Domain,(E/Z)-ZL0420,BRD4,airway inflammation,immune response genes,Z
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格：￥电议型 号：T6828产 地：中国大陆
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T9019JHU37152JHU37152,inhibit,hM3Dq,Clozapine,Inhibitor,DREADD,Muscarinic acetylcholine receptor,mAChR,hM
JHU 37152 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.8 nM and 8.7 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 5 nM and 0.5 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格：￥电议型 号：T9019产 地：中国大陆
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T80802-?Methylhexanoic acidInhibitor,2-?Methylhexanoic acid,2 ?Methylhexanoic acid,2?Methylhexanoic acid,
2-Methylhexanoic acid is a flavouring ingredient.
价 格：￥电议型 号：T8080产 地：中国大陆
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T8308NL-1Inhibitor,viability,Mitochondrial Metabolism,leukemia,NL-1,CISD1,NL1,antileukemic,MitoNEET,lymph
NL-1 is a mitoNEET inhibitor with antileukemic effect.
价 格：￥电议型 号：T8308产 地：中国大陆
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T9784Docosanedioic acid?Antibody-drug conjugates linkers,Docosanedioic acid,inhibit,Docosanedioic acid?,I
BEHENIC ACID is a alkyl-chain-based PROTAC linker. BEHENIC ACID is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9784产 地：中国大陆
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T8422DIETHYLDITHIOCARBAMIC ACID COPPER SALTDIETHYLDITHIOCARBAMIC ACID COPPER SALT
DIETHYLDITHIOCARBAMIC ACID COPPER SALT is a chemical compound.
价 格：￥电议型 号：T8422产 地：中国大陆
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T8240Cis-5-Dodecenoic AcidCis 5 Dodecenoic Acid,Cis5Dodecenoic Acid,inhibit,Inhibitor,COX,Endogenous Meta
Cis-5-Dodecenoic Acid is a monounsaturated fatty acid that has a C12 chain as a backbone and a cis double bond at the C5 position.
价 格：￥电议型 号：T8240产 地：中国大陆
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TP1309Gastric mucinAntibiotic,inhibit,Inhibitor,Gastric mucin,Bacterial
Gastric mucin is a large glycoprotein which is thought to play a major role in the protection of the gastrointestinal tract from acid, proteases, pathogenic microorganisms, and mechanical trauma.
价 格：￥电议型 号：TP1309产 地：中国大陆
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T6686Sulconazole mononitrateanaerobes,antimicrobial,Inhibitor,Fungal,antibacterial,Bacterial,Gram-positiv
Sulconazole Nitrate is the nitrate salt form of sulconazole, a synthetic imidazole derivative with the antifungal property. Sulconazole nitrate inhibits fungal cytochrome P-450 sterol C-14 alpha-demethylation, resulting in the accumulation of fungal 14 alpha-methyl sterols and inhibition of the synthesis of ergosterol, an important component of the fungal cell membrane. Inhibition of ergosterol synthesis leads to a disruption of cell membrane permeability, and ultimately inhibition of cell wall
价 格：￥电议型 号：T6686产 地：中国大陆
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T9424Temgicolurilinhibit,Inhibitor,γ-Aminobutyric acid Receptor,Mebicar,Temgicoluril,Gamma-aminobutyric a
Temgicoluril acts on?GABA Receptor.
价 格：￥电议型 号：T9424产 地：中国大陆
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T8995NCGC00262650NCGC00262650,inhibit,Inhibitor,apical membrane antigen 1,AMA1-RON2,merozoites,NCGC 00262
NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.
价 格：￥电议型 号：T8995产 地：中国大陆
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TP1329Nisininhibit,Inhibitor,Antibiotic,Nisin,Bacterial
Nisin A is an antibacterial peptide. It is produced by the lactic acid bacterium L. lactis using uncommon amino acids, including lanthionine, and is a member of the class of antibiotics referred to as lantibiotics.
价 格：￥电议型 号：TP1329产 地：中国大陆
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T9943(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid(E)6(4methylbenzyli
(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid is a 2-?benzylidene tetrahydronaphthone derivative and can be used as a firefly luciferase inhibitor in kit.
价 格：￥电议型 号：T9943产 地：中国大陆
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T7837SR8278Duchenne muscular dystrophy,inhibit,metabolism,biological rhythm,Alzheimer’s disease,SR-8278,S
SR8278 is an REV-ERBα antagonist(EC50 = 0.47 μM), blocking activation of the receptor by the synthetic agonist GSK 4112
价 格：￥电议型 号：T7837产 地：中国大陆
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T6386Ampicillin sodiumAmpicillin sodium,Antibiotic,inhibit,Inhibitor,Bacterial,Ampicillin
Ampicillin Sodium is the sodium salt form of ampicillin, a broad-spectrum semisynthetic derivative of aminopenicillin. Ampicillin sodium inhibits bacterial cell wall synthesis by binding to penicillin binding proteins, thereby inhibiting peptidoglycan synthesis, a critical component of the bacterial cell wall.
价 格：￥电议型 号：T6386产 地：中国大陆
