T6068MK-5108MK 5108,VX689,Aurora Kinase,VX 689,inhibit,Autophagy,MK-5108,Inhibitor

MK-5108 is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.

价 格：￥电议型 号：T6068产 地：中国大陆

TN1773Isoastragaloside IVinhibit,Inhibitor,Isoastragaloside IV

Isoastragaloside IV is a natural product

价 格：￥电议型 号：TN1773产 地：中国大陆

T9328Ellagic Acid DihydrateEllagic Acid Dihydrate

Ellagic Acid Dihydrate inhibit the CYP1A1-dependent activation of benzo[a]pyrene.

价 格：￥电议型 号：T9328产 地：中国大陆

T7649Tyrphostin A1Tyrphostin A 1,Interleukin Related,AG 9,Tyrphostin1,Tyrphostin A1,inhibit,Tyrphostin A-

Tyrphostin A1 is an inhibitor of EGFR tyrosine kinase .

价 格：￥电议型 号：T7649产 地：中国大陆

T10329anti-TB agent 1antiTB agent 1,anti TB agent 1

anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).

价 格：￥电议型 号：T10329产 地：中国大陆

T9050AG-270inhibit,Inhibitor,cancer,Low,solid,AG-270,SAM,pancreatic,lymphoma,tumor,AG 270,toxicity,AG270

AG-270 is an allosteric and orally active inhibitor of MAT2A.

价 格：￥电议型 号：T9050产 地：中国大陆

T8873BractoppinDNA break,Bractoppin,phosphopeptide,inhibit,DNA/RNA Synthesis,DNA damage,RAD51,G2 arrest,I

Bractoppin is a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain (IC50 = 0.074 μM), which selectively inhibits substrate binding with nanomolar potency in vitro. Structure-activity exploration suggests that Bractoppin engages BRCA1 tBRCT residues recognizing pSer in the consensus motif, pSer-Pro-Thr-Phe, plus an abutting hydrophobic pocket that is distinct in structurally related BRCT domains, conferring selectivity.

价 格：￥电议型 号：T8873产 地：中国大陆

T6762AS1842856AS 1842856,AS-1842856,inhibit,AS1842856,Autophagy,Inhibitor

AS1842856, a cell-permeable inhibitor, can block the transcription activity of Foxo1 (IC50: 33 nM). It can directly bind to the active Foxo1, but not the Ser256-phosphorylated form.

价 格：￥电议型 号：T6762产 地：中国大陆

T9013Autogramin-2Autogramin-2,Inhibitor,inhibit,Autogramin2,Autophagy,Autogramin 2

Autogramin-2 potently inhibits?autophagy?induced by either starvation with IC50 of 0.27 μM, and inhibits mTORC1 (Rapamycin; IC50:0.14 μM)

价 格：￥电议型 号：T9013产 地：中国大陆

T88684BP-TQS4BP TQS,allosteric agonist,transmembrane site,Inhibitor,α7 nAChR,inhibit,Nicotinic acetylchol

4BP-TQS is an allosteric agonist of α7 nAChRs.

价 格：￥电议型 号：T8868产 地：中国大陆

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

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

T5903Sitagliptin Intermediate 2Sitagliptin Intermediate 2

价 格：￥电议型 号：T5903产 地：中国大陆

T6667SF1670inhibit,Autophagy,SF1670,MMAC1,Inhibitor,SF 1670,SF-1670,Phosphatase and tensin homolog,Phosph

SF1670 is a specific PTEN inhibitor with IC50 of 2 μM.

价 格：￥电议型 号：T6667产 地：中国大陆

T7697BIX-01294PRMT1,recurrent,Autophagy,H3K9me3,Inhibitor,Cdkn1a,inhibit,p53,Gadd45a,MLKL,Histone Methylt

BIX-01294 is an G9a Histone Methyltransferase inhibitor(IC50 : 1.9 μM).

价 格：￥电议型 号：T7697产 地：中国大陆

T6855HA15HA-15,HSP,HA 15,Inhibitor,HA15,Apoptosis,inhibit,Autophagy,Heat shock proteins

HA15 targets specifically BiP/GRP78/HSPA5. HA15 exhibits anti-cancerous activity on all melanoma cells tested, including cells isolated from patients and cells that developed resistance to BRAF inhibitors.

价 格：￥电议型 号：T6855产 地：中国大陆

TP1530LYRGDS Fibronectin Fragment acetateYRGDS Fibronectin Fragment acetate

This is a fibronectin fragment acetate, an adhesion peptide that displays strong binding affinity to thrombin-stimulated platelets. It is RGD consisting of sequence.

价 格：￥电议型 号：TP1530L产 地：中国大陆

T7882Indomethacin farnesilAutophagy,inhibit,flux,Inhibitor,Indomethacin farnesil,cox1,COX,pain,Cyclooxyge

Infree is a prodrug of indomethacin. It acts as a nonsteroidal anti-inflammatory drug (NSAID) and disease-modifying anti-rheumatic drug (DMARD).

价 格：￥电议型 号：T7882产 地：中国大陆

TQ0097AGN 193109AGN193109,Autophagy,Inhibitor,Retinoic acid receptors,Retinoid X receptors,RAR/RXR,AGN 193

AGN 193109, a retinoid analog, is a potent and specific antagonist of RARs (Kds: 2 nM, 2 nM, and 3 nM for RARα, RARβ, and RARγ).

价 格：￥电议型 号：TQ0097产 地：中国大陆

T101625-HT3 antagonist 35 HT3 antagonist 3,5-HT-3 antagonist 3,5HT3 antagonist 3

5-HT3 antagonist 3 (Compound 15b) is a high-affinity 5-HT3 receptor antagonist. It binds to 5-HT3 receptors in rat brain cortical membranes (Ki: 0.25 nM).

价 格：￥电议型 号：T10162产 地：中国大陆