T9281(S)-2-((R)-3-(4-chlorophenyl)-N’-((4-chlorophenyl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carbo

(S)-2-((R)-3-(4-chlorophenyl)-N’-((4-chlorophenyl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidamido)-3-methylbutanamide is a cannabinoid receptor antagonist/inverse agonist.

价 格：￥电议型 号：T9281产 地：中国大陆

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

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

T73792-D08Ubiquitin ligase,Axl,2-D08,Tyro3,E3 ligating enzyme,Ubiquitin activating enzyme,Inhibitor,E1 ac

2-D08 is a synthetic flavone that inhibits sumoylation, also inhibits Axl with an IC50 of 0.49 nM.2-D08 showed anti-aggregatory and neuroprotective effect.

价 格：￥电议型 号：T7379产 地：中国大陆

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

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

T13378Z-Asp-CH2-DCBZAspCH2DCB,Z Asp CH2 DCB,Z-Asp-CH-2-DCB

Z-Asp-CH2-DCB is an irreversible inhibitor of broad spectrum caspase.

价 格：￥电议型 号：T13378产 地：中国大陆

T9023AtuliflaponInhibitor,inhibit,FLAP,AZD-5718,AZD 5718,artery,Atuliflapon,disease,Coronary,5-LO activat

AZD5718 is a novel 5-Lipoxygenase Activating Protein(FLAP) inhibitor for Treatment of Coronary Artery Disease.

价 格：￥电议型 号：T9023产 地：中国大陆

T9954K-975YAP1,Cys359,pleural,TAZ,K 975,inhibit,K-975,Yes-associated protein,YAP,Inhibitor,antitumor,mali

K-975 is a highly selective, orally active TEAD inhibitor, effectively inhibiting protein-protein interactions between TEAD and YAP1/TAZ.

价 格：￥电议型 号：T9954产 地：中国大陆

T4846BenzylamineBenzylamine

价 格：￥电议型 号：T4846产 地：中国大陆

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

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

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

T7968DazoxibenDazoxiben,Inhibitor,inhibit

Dazoxiben is a potent inhibitor of thromboxane (TX) synthase

价 格：￥电议型 号：T7968产 地：中国大陆

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

T10436AZD4573AZD 4573,inhibit,CDK,AZD4573,AZD-4573,Inhibitor,Cyclin dependent kinase

AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enables transient target engagement for the treatment of hematologic malignancies.

价 格：￥电议型 号：T10436产 地：中国大陆

TN2080Pinoresinolapoptotic,sensitizer,Pinoresinol,caterpillar,inhibit,cancer,Apoptosis,Inhibitor,lignol,gl

Pinoresinol has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative stress preserving pial blood flow distribution; it may exert pharmacologically interesting effects via modulation of the insulin-like signalling pathway in C.elegans. Pinoresinol causes an upregulation of the CDK inhibitor p21(WAF1/Cip1) both at mRNA and protein levels, inhibits NF-kappaB and activa

价 格：￥电议型 号：TN2080产 地：中国大陆

T61148Flutrimazole

Flutrimazole is an imidazole antifungal with dual anti-inflammatory and antifungal activity. Flutrimazole shows scarce transdermal penetration. Flutrimazole has the advantageous in the research of topical fungal infections with an inflammatory component.

价 格：￥电议型 号：T61148产 地：中国大陆

T8529WYC-210Inhibitor,Tazarotene,retinoid,anticancer,inhibit,WYC210,WYC 210,WYC-210

WYC-210 is a retinoid compound,and with lower anticancer activity

价 格：￥电议型 号：T8529产 地：中国大陆

TN71857-Cyano-7-deazaguanine

3H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 2-amino-4,7-dihydro-4-oxo- is a marine derived natural products found in Streptomyces qinglanensis.

价 格：￥电议型 号：TN7185产 地：中国大陆