T12589PI3Kα/mTOR-IN-1PI3Kα/mTORIN1,PI3Kα/mTOR IN 1,PI-3Kα/mTOR-IN-1

PI3Kα/mTOR-IN-1 is a potent dual inhibitor of PI3Kα/mTOR. PI3Kα/mTOR-IN-1 shows an IC50 of 7 nM for PI3Kα in a cell assay, and Kis of 12.5 nM and 10.6 nM for mTOR and PI3Kα in a cell free assay , respectively.

价 格：￥电议型 号：T12589产 地：中国大陆

TN4618N-trans-SinapoyltyramineN trans Sinapoyltyramine,NtransSinapoyltyramine

N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.

价 格：￥电议型 号：TN4618产 地：中国大陆

T7831NitecaponeGSH,Nitecapone,glutathione,OR-462,Inhibitor,ROS,Parkinson,COMT,OR 462,inhibit,OR462,allody

Nitecapone is a reversible inhibitor of S-COMT (IC50 values of 300 nM in rat liver)

价 格：￥电议型 号：T7831产 地：中国大陆

TMA2613Cyclo(Pro-Leu)

Cyclo(Pro-Leu) is a marine-derived natural product with brine shrimp lethality.

价 格：￥电议型 号：TMA2613产 地：中国大陆

T6972RS-1RAD51,RS1,RS-1,inhibit,Inhibitor,RS 1,CRISPR/Cas9

RS-1 is a RAD51 activator. RS-1 also increases CRISPR/Cas9-mediated knock-in efficiencies.

价 格：￥电议型 号：T6972产 地：中国大陆

T61112SLF1081851

SLF1081851 is a Spns2 inhibitor. SLF1081851 inhibits S1P release with IC50 of 1.93 μM.

价 格：￥电议型 号：T61112产 地：中国大陆

T17005FPR Agonist 43FPR Agonist 43

FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.

价 格：￥电议型 号：T17005产 地：中国大陆

Fr13755Compound Fr13755Compound Fr13755

价 格：￥电议型 号：Fr13755产 地：中国大陆

T67762Compound EN300-317386CompoundEN300317386

Compound EN300-317386 is a compound with drug-like properties.

价 格：￥电议型 号：T67762产 地：中国大陆

T24871TFMB-(S)-2-HG

TFMB-(S)-2-HG is a potent inhibitor of the 5´-methylcytosine hydroxylase TET2. TFMB-(S)-2-HG also inhibits the EglN prolyl hydroxylases. TFMB-(S)-2-HG has the potential for the research of acute myeloid leukemia (AML).

价 格：￥电议型 号：T24871产 地：中国大陆

TN1990NorathyriolNatural,Antioxidant,Peroxisome proliferator-activated receptors,anti-bacterial,inhibit,an

Norathyriol is a potent PTP1B inhibitor with good cell permeability and oral availability.

价 格：￥电议型 号：TN1990产 地：中国大陆

T9075BDP-13176inhibit,BDP13176,BDP-13176,Inhibitor,BDP 13176

BDP-13176 is a potent?inhibitor of fascin 1(Kd?of 90 nM and an?IC50?of 240 nM). It has potential as an anti-metastatic agent

价 格：￥电议型 号：T9075产 地：中国大陆

T9716Ensitrelvirintrapulmonary replication,Virus Protease,COVID-19,S217622,oral,SARS-CoV,Ensitrelvir,SARS

Ensitrelvir is an orally active inhibitor of SARS-CoV-2 3CL protease with IC50 of 13 nM.

价 格：￥电议型 号：T9716产 地：中国大陆

T64375UNC?1021UNC?1021

UNC 1021 is a selective L3MBTL3 inhibitor (IC50 = 0.048 μM).

价 格：￥电议型 号：T64375产 地：中国大陆

T6S1141Ganoderic acid AInhibitor,Autophagy,Ganoderic acid A,Apoptosis,inhibit,Endogenous Metabolite

1. Ganoderic acid A exhibits antitumor activity, mediated through its inhibitory effect on nuclear transcription factor-kappaB and activator protein-1. 2. Ganoderic acid A can induce proliferation inhibition, apoptosis and suppression of invasion in human osteosarcoma HOS and MG-63 cells. 3. Ganoderic acid A promotes cisplatin-induced cell death by enhancing the sensitivity of HepG2 cells to cisplatin mainly via the signal transducer and activator of transcription 3 suppression, significantly su

价 格：￥电议型 号：T6S1141产 地：中国大陆

PDK0217Compound PDK0217Compound PDK0217

价 格：￥电议型 号：PDK0217产 地：中国大陆

T12513PNZ5PNZ5,PNZ-5

PNZ5 is a potent and isoxazole-based pan-BET inhibitor, with high selectivity and potency similar to the well-established (+)-JQ1, with a KD of 5.43 nM for BRD4(1).

价 格：￥电议型 号：T12513产 地：中国大陆

T7007UNC2025Inhibitor,inhibit,FLT3,leukemia,CD135,Fms like tyrosine kinase 3,acute,Cluster of differentia

UNC-2025（ IC50 of 0.74 nM and 0.8 nM） is a potent and orally bioavailable dual MER/FLT3 inhibitor. UNC-2025 is about 20-fold selectivity higher than Axl and Tyro3.

价 格：￥电议型 号：T7007产 地：中国大陆

T60148MSC-4106MSC4106

MSC-4106 is an orally active and potent inhibitor of YAP/TAZ-TEAD. MSC-4106 inhibits TEAD1 or TEAD3 auto-palmitoylation and exhibits inhibitory effect on NCI-H226 tumor xenograft model [1].

价 格：￥电议型 号：T60148产 地：中国大陆

TQ0059Ilorasertibanti-tumor,H1299,Platelet-derived growth factor receptor,Inhibitor,ABT 348,antiproliferat

Ilorasertib (ABT-348) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora A/Aurora B/Aurora C (IC50s: 120 nM/7 nM/1 nM). It also suppresses RET tyrosine kinase, PDGFRβ, and Flt1 (IC50s: 7 nM, 3 nM, and 32 nM).

价 格：￥电议型 号：TQ0059产 地：中国大陆