T16536Pimonidazole hydrochlorideinhibit,Pimonidazole hydrochloride,Pimonidazole,Inhibitor

Pimonidazole hydrochloride accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after the reduction of its nitro group. It can be used for qualitative and quantitative assessment of tumor hypoxia. Pimonidazole hydrochloride is a novel hypoxia marker for the complementary study of tumor hypoxia and cell proliferation in tumors.

价 格：￥电议型 号：T16536产 地：中国大陆

T8980SGA360inhibit,Inhibitor,SGA360,SGA 360,SGA-360

SGA360 is a selective aryl hydrocarbon (Ah) receptor modulator. It exhibits anti-inflammatory properties.

价 格：￥电议型 号：T8980产 地：中国大陆

TN24364-methyl-6-phenyl-2H-pyranone

4-methyl-6-phenyl-2H-pyranone is derived from Scutellaria baicalensis Georgi and improves mitochondrial functionality to protect astrocytes against hydrogen peroxide-induced toxicity.

价 格：￥电议型 号：TN2436产 地：中国大陆

T26969CCT365623CCT365623

CCT365623 is an orally bioavailable Lysyl Oxidase inhibitor with good anti-LOX potency, selectivity, pharmacokinetic properties, as well as anti-metastatic efficacy.

价 格：￥电议型 号：T26969产 地：中国大陆

T36711FM19G11

FM19G11 is an inhibitor of hypoxia inducible factor (HIF) α-subunit (IC50 = 80 nM in hypoxia induced luciferase assay).

价 格：￥电议型 号：T36711产 地：中国大陆

T8836CY5-SE triethylamine saltoligonucleotides,reactive,dye,amino-groups,inhibit,CY-5-SE triethylamine sa

Fluorolink Cy5 triethanolamine salt is a hydrophilic amine-reactive fluorescent probe. It displays excitation/emission maxima of 646/662 nm, respectively. Cy5-SE-conjugated ligands have been used in the characterization of hematopoietic tumor microenvironments.

价 格：￥电议型 号：T8836产 地：中国大陆

T7363Ibuprofen PiconolIbuprofen Piconol,U 75630,U-75630,Inhibitor,inhibit

Ibuprofen piconol is a non-steroidal, anti-inflammatory (NSAID) agent for the topical relief of primary thermal burns and sunburns.Ibuprofen piconol is a Pyridyl ester of ibuprofen.

价 格：￥电议型 号：T7363产 地：中国大陆

T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha

AY 9944 dihydrochloride is a intermediate.

价 格：￥电议型 号：T14362L产 地：中国大陆

T36957BODIPY 493/503

BODIPY 493/503 is a lipophilic fluorescent probe with Ex/Em of 493/503 nm. BODIPY 493/503 localizes to polar lipids and can be used to label cellular neutral lipid contents and for live and fixed cell applications.

价 格：￥电议型 号：T36957产 地：中国大陆

T9573GSK3685032Inhibitor,GSK 3685032,lymphoma,DNMTs,cancer,DNA MTases,GSK-3685032,inhibit,GSK3685032,DNA

GSK3685032 is a non-covalent and selective DNMT1 inhibitor(IC50 = 36 nM). The inhibitory effect is time-independent and reversible. GSK3685032 induces loss of DNA methylation and transcriptional activation and inhibits cancer cell growth.

价 格：￥电议型 号：T9573产 地：中国大陆

T59362,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE2,3 DIHYDRO 1H PYRROLO[2,3 B]PYRIDINE,2,3DIHYDRO1HPYRROLO[2,3B]

价 格：￥电议型 号：T5936产 地：中国大陆

TN3609Catalposide

Catalposide is a potent inducer of (HO)-1 isolated from Catalpa ovate G. Don (Bignoniaceae). Catalposide possesses antioxidant, anti-apoptotic, anti-microbial, anti-tumoral, and anti-inflammatory properties.

价 格：￥电议型 号：TN3609产 地：中国大陆

TQ0062NastorazepideZ360,CCK Receptor,Cholecystokinin Receptor,Inhibitor,Z 360,Nastorazepide,inhibit

Nastorazepide is a selective, orally available antagonist of gastrin/cholecystokinin 2 (CCK-2) receptor with potential antineoplastic activity.

价 格：￥电议型 号：TQ0062产 地：中国大陆

TQ0187SR-3677Inhibitor,Rho-associated protein kinase,Autophagy,SR 3677,Rho-kinase,SR3677,ROCK,ROK,SR-3677,

SR-3677 is an effective and specific inhibitor of ROCK2 (IC50: 3 nM).

价 格：￥电议型 号：TQ0187产 地：中国大陆

Fr13619Compound Fr13619Compound Fr13619

价 格：￥电议型 号：Fr13619产 地：中国大陆

TP1059Peptide YY (PYY) (3-36), humanNeuropeptide Y Receptor,Inhibitor,NPY receptor,Peptide YY (PYY) (336),

Peptide YY (PYY) (3-36), human is a gut hormone peptide. Peptide YY (PYY) (3-36), human acts as a Y2 receptor agonist to reduce appetite.

价 格：￥电议型 号：TP1059产 地：中国大陆

T7409360A360A,Telomerase,inhibit,Inhibitor,G-quadruplex

360A is a stabilizing G-Quadruplex ligand, and also inhibits telomerase activity for telomerase in TRAP-G4 assay(IC50 : 300 nM).

价 格：￥电议型 号：T7409产 地：中国大陆

T9140NAcM-OPT HCl(2089293-61-6 free base)NAcMOPT HCl(2089293616 free base),NAcM OPT HCl(2089293 61 6 free

NAcM-OPT HCL is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor that targets N-Acetyl-UBE2M (E2 conjugating enzyme, UBC12) interaction with DCN1 with IC50 of 79 nM.

价 格：￥电议型 号：T9140产 地：中国大陆

T36526IL-17 modulator 4IL17 modulator 4,IL 17 modulator 4

IL-17 modulator 4 is a prodrug of IL-17 modulator 1 which is an efficacious modulator of IL-17.

价 格：￥电议型 号：T36526产 地：中国大陆

TN7036N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamidebone formation,Beta catenin,inhibit,Inhibitor,N (

N-3-methoxylBenzyllinolenicamide induces osteogenic differentiation and subsequent bone formation of mesenchymal stem cells by activating the canonical Wnt/β-catenin signaling pathway that can be used for osteoporosis research.

价 格：￥电议型 号：TN7036产 地：中国大陆