T6440CGP 57380CGP-57380,CGP 57380,Mitogen activated protein kinase interacting kinase,Inhibitor,MAPK inte

CGP 57380 is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.

价 格：￥电议型 号：T6440产 地：中国大陆

T9060STM2457leukaemia,Apoptosis,cancer,STM-2457,autoimmune diseases,STM2457,inhibit,STM 2457,myeloid,Inhi

STM2457 is a first-in-class, highly potent, selective and orally active inhibitor of METTL3 . It can be used for the research of acute myeloid leukaemia (AML).

价 格：￥电议型 号：T9060产 地：中国大陆

TP2306Adipotide/FTPP(FatTargetedProapoptoticPeptide) AcetateAdipotide/FTPP(FatTargetedProapoptoticPeptide)

Adipotide as a prototype in a new class of candidate drugs that may be useful for treating obesity in humans

价 格：￥电议型 号：TP2306产 地：中国大陆

TQ0089JuglaninJNK,Juglanin,ROS/JNK,Inhibitor,G2/M,arrest,Apoptosis,Autophagy,phase,inhibit,breast cancer

Juglanin is a JNK activator. Juglanin with inflammation and anti-tumor activities. It can induce apoptosis and autophagy on human breast cancer cells.

价 格：￥电议型 号：TQ0089产 地：中国大陆

T60150(1S,2R)-Alicapistat(1S,2R)Alicapistat

(1S,2R)-Alicapistat ((1S,2R)-ABT-957) is an orally active selective inhibitor of human calpains 1 and 2 with the potential application of Alzheimer´s disease (AD) [1]. (1S,2R)-Alicapistat mitigates the metabolic liability of carbonyl reduction and inhibits calpain 1 with an IC 50 value of 395 nM [2].

价 格：￥电议型 号：T60150产 地：中国大陆

T6858Hydroxyprogesterone caproateHydroxyprogesterone caproate,Inhibitor,inhibit

Hydroxyprogesterone Caproate is a synthetic progestational agent. It binds to and activates nuclear progesterone receptors in the reproductive system and inhibits ovulation and an alteration in the cervical mucus and endometrium.

价 格：￥电议型 号：T6858产 地：中国大陆

T7856Naphthol AS-EHAT,KIX-KID,MCF-7,cancer,Inhibitor,Naphthol AS-E,inhibit,Epigenetic Reader Domain,CREB,

nAS-E is an the KIX-KID interaction and CREB-mediated gene transcription inhibitor.

价 格：￥电议型 号：T7856产 地：中国大陆

T6909NSC348884lymphoma,cancer,inhibit,SKOV3,MOSEC/Luc cell,NSC-348884,NSC 348884,LNCaP,doxorubicin,NSC348

NSC348884 is a nucleophosmin inhibitor disrupts oligomer formation and induces apoptosis, inhibits cell proliferation at an IC50 of 1.7-4.0 μM in distinct cancer cell lines.

价 格：￥电议型 号：T6909产 地：中国大陆

T9377ASK1-IN-2colitis,ulcerative,signal-regulating,ASK1 IN 2,ASK1IN2,inhibit,MAP kinase kinase kinase, ME

ASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1), with an IC50 of 32.8 nM. ASK1-IN-2 can potentially be used as a therapeutic strategy for ulcerative colitis[1].

价 格：￥电议型 号：T9377产 地：中国大陆

T6371AGK2Sirtuin,AGK 2,inhibit,AGK2,AGK-2,Inhibitor,Apoptosis

AGK2（IC50=3.5 μM） is an effective, and specific SIRT2 inhibitor.

价 格：￥电议型 号：T6371产 地：中国大陆

T8359Lanreotide acetateLanreotide,Lanreotide acetate,inhibit,hormone,apoptosis,pituitary,BIM23014,Inhibit

Lanreotide acetate is a somatostatin analogue with antineoplastic activity, used for carcinoid syndrome

价 格：￥电议型 号：T8359产 地：中国大陆

TN1721Gypenoside LMAPK,Extracellular signal regulated kinases,NF-κB,Nuclear factor-κB,saponin,anti-tumor,N

Gypenoside L inhibits autophagic flux and induces cell death in human esophageal cancer cells through endoplasm reticulum stress-mediated Ca2+ release. It also inhibit non-small cell lung carcinoma A549 cell inhibitory activity.

价 格：￥电议型 号：TN1721产 地：中国大陆

T7587Tenapanorinhibit,Sodium-hydrogen Exchanger,intestinal,hyperphosphatemia,Sodium/hydrogen Exchanger,In

Tenapanor is an inhibitor of the sodium-proton (Na(+)/H(+)) exchanger NHE3, which plays a prominent role in sodium handling in the gastrointestinal tract and kidney. Tenapanor possesses an excellent preclinical safety profile and, as of now, there are no serious concerns about its side effects.

价 格：￥电议型 号：T7587产 地：中国大陆

T2430HPOBHDAC,Apoptosis,cells,anticancer,Histone deacetylases,HPOB,tumor,A549,U87,Inhibitor,inhibit,LNCaP

HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.

价 格：￥电议型 号：T2430产 地：中国大陆

T6821Dp44mTDp44mT,inhibit,Apoptosis,Dp-44mT,Inhibitor,Ferroptosis

Dp44mT, a effective iron chelator, has selective antitumor activity.

价 格：￥电议型 号：T6821产 地：中国大陆

T8986ML198inhibit,ML198,ML-198,ML 198,GCase modulator,Inhibitor,Non-inhibitory chaperone,Gaucher disease,

ML198 is a novel activator and non-inhibitory chaperone of glucocerebrosidase. ML198 serves as a starting point to develop a novel approach towards small molecule treatment for patients suffering from Gaucher disease.

价 格：￥电议型 号：T8986产 地：中国大陆

TN1772Isoastilbindisease,anti-apoptotic,glycoside,Tyrosinase,Bacterial,antimicrobial,Inhibitor,Antioxidati

Isoastilbin is a dihydroflavonol glycoside compound in Rhizoma Smilacis glabrae and Astragalus membranaceus. Isoastilbin inhibits glucosyltransferase (GTase) with an IC50 value of 54.3 μg/mL, Isoastilbin has anti-acne and tyrosinase inhibition properties. Isoastilbin shows neuroprotective, antioxidation, antimicrobial and anti-apoptotic properties and has the potential for Alzheimer s disease research

价 格：￥电议型 号：TN1772产 地：中国大陆

T218381-Naphthyl 3,5-dinitrobenzoate1Naphthyl 3,5dinitrobenzoate,1 Naphthyl 3,5 dinitrobenzoate

1-Naphthyl 3,5-dinitrobenzoate is an inhibitor of 5-LOX can be used in studies about inflammatory therapy.

价 格：￥电议型 号：T21838产 地：中国大陆

T70384-Methylayapin4Methylayapin,4 Methylayapin

价 格：￥电议型 号：T7038产 地：中国大陆

T9470HPK1-IN-7HPK1 IN 7,MC38,Inhibitor,PD1,HPK1IN7,tumor,model,oral,selectivity,HPK-1-IN-7,MAP4K,inhibit,

HPK1-IN-7 is an orally active HPK1 inhibitor. It shows selectivity against IRAK4 (59 nM) and GLK (140 nM).

价 格：￥电议型 号：T9470产 地：中国大陆