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T6396(R)-(-)-Gossypol acetic acidBcl-2 Family,Autophagy,(R) ( ) Gossypol acetic acid,Inhibitor,(R)()Gossy
AT101, the R-(-) enantiomer of Gossypol acetic acid, binds with Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.32 μM, 0.48 μM and 0.18 μM; does not inhibit BIR3 domain and BID. Phase 2.
价 格：￥电议型 号：T6396产 地：中国大陆
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TN69601-Pentadecanol1-Pentadecanol,inhibit,Inhibitor,1 Pentadecanol,1Pentadecanol
1-Pentadecanol is a naturally antiacne agent.
价 格：￥电议型 号：TN6960产 地：中国大陆
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T19694Hydronidone
Hydronidone is Non-Steroidal Antiinflammatory Drugs. It potentially for the treatment of hepatic fibrosis.
价 格：￥电议型 号：T19694产 地：中国大陆
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TP1496Lp5 Ligand for Dnak and DnaJ acetatep5 Ligand for Dnak and DnaJ acetate,p-5 Ligand for Dnak and DnaJ
p5 Ligand for Dnak and DnaJ acetate is a nonapeptide. It is a high-affinity ligand for DnaK (E. coli Hsp70) and DnaJ (E. coli Hsp40).
价 格：￥电议型 号：TP1496L产 地：中国大陆
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T4962Zingibroside R1Human immunodeficiency virus,Zingibroside R 1,Zingibroside R-1,Zingibroside R1,Inhibi
Zingibroside R1 has anti-HIV-1 activity.
价 格：￥电议型 号：T4962产 地：中国大陆
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T10696CB2 modulator 1CB2 modulator 1,ischemia,CB-2 modulator 1,osteoporosis,CB2,inflammation,immunedisorde
CB2 modulator 1 is a potent CB2 modulator. It can be used for the research for immune disorders, osteoporosis, inflammation, renal ischemia.
价 格：￥电议型 号：T10696产 地：中国大陆
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T16963SYM 2081SYM 2081
SYM 2081 is a specific kainate receptor agonist with an IC50 value of 35 nM for [3H]-kainate binding. SYM 2081 depolarizes the muscle and reduces the EPSP amplitude.
价 格：￥电议型 号：T16963产 地：中国大陆
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T9696β-catenin-IN-2HCT116,inhibit,cancer,β-catenin,cell,Beta catenin,HT-29,Tcf/4,Colorectal,Inhibitor,β c
β-catenin-IN-2 is a potent inhibitor of β-catenin that can be used in colorectal cancer research.
价 格：￥电议型 号：T9696产 地：中国大陆
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T7296THZ2inhibit,THZ2,Cyclin dependent kinase,CDK,THZ-2,Inhibitor,THZ 2
THZ2, an analog of THZ1, is a potent and selective CDK7 inhibitor(IC50:13.9 nM),with the potential to treat Triple-negative breast cancer (TNBC).
价 格：￥电议型 号：T7296产 地：中国大陆
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T9604beta-Estradiol 17-hemisuccinatebetaEstradiol 17hemisuccinate,beta Estradiol 17 hemisuccinate
beta-Estradiol 17-hemisuccinate selectively stains estrogen receptor (ER)-rich cells.
价 格：￥电议型 号：T9604产 地：中国大陆
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TQ0037Abrocitinibinhibit,Abrocitinib,Inhibitor,JAK,PF04965842,Janus kinase,PF 04965842
Abrocitinib (PF-04965842) is a potent, specific and orally-active JAK1 inhibitor (IC50s: 29/803 nM for JAK1/2).
价 格：￥电议型 号：TQ0037产 地：中国大陆
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T8966ML-298ML-298,Inhibitor,ML 298,Phospholipase,inhibit
ML298 is a potent, specific inhibitor of Phospholipase D2 (PLD2, IC50 of 355 nM).
价 格：￥电议型 号：T8966产 地：中国大陆
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T9966GSK-1520489AGSK1520489A,inhibit,GSK 1520489A,HT29,GSK-1520489A,Inhibitor,active protein kinase
GSK-1520489A is an active PKMYT1 inhibitor.
价 格：￥电议型 号：T9966产 地：中国大陆
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T6696Tazaroteneinhibit,Inhibitor,Tazarotene,AGN-190168,RAR/RXR,AGN190168,Retinoic acid receptors,Autophag
Tazarotene is a synthetic, topical retinoid. Tazarotene induces the expression of tazarotene-induced gene 3 (TIG3), a tumor suppressor gene. In psoriasis, tazarotene normalizes abnormal keratinocyte differentiation and reduces their hyperproliferation.
价 格：￥电议型 号：T6696产 地：中国大陆
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T11909LY2444296
LY2444296 is an orally active and selective antagonist of kappa opioid receptor(Ki = 1 nM).
价 格：￥电议型 号：T11909产 地：中国大陆
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T9636DalpiciclibMCF7,BT-474/T,Cyclin dependent kinase,Eca 109,MCF7/TR,and KYSE-510 ESCC,SHR6390,Inhibitor
Dalpiciclib is a highly selective, orally bioavailable, and comparable potency inhibitor of CDK4 and CKD6 with IC50s of 12.4?nM and 9.9?nM, respectively. Dalpiciclib exerts potent antitumor activity in esophageal squamous cell carcinoma by inhibiting phosphorylated tumor suppressor retinoblastoma protein (Rb) and inducing G1 cell cycle arrest.
价 格：￥电议型 号：T9636产 地：中国大陆
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T23796BIRT-377
BIRT-377 is a negative allosteric and orally bioavailable inhibitor of ICAM-1 and LFA-1(Ki = 25.8 nM). BIRT-377 inhibits the production of IL-2 and can be used in studies about inflammatory and immune disorders.
价 格：￥电议型 号：T23796产 地：中国大陆
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T8876PF-06882961 TrisPF 06882961 Tris,PF06882961 Tris
PF-06882961 Tris is an orally bioavailable glucagon-like peptide-1 receptor (GLP-1R) agonist.
价 格：￥电议型 号：T8876产 地：中国大陆
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TN1096Ginsenoside Ra1Ginsenoside Ra1,inhibit,Inhibitor,Ginsenoside Ra 1,Ginsenoside Ra-1
Ginsenoside Ra1 is a component from ginseng. Ginsenoside Ra1 shows significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R).
价 格：￥电议型 号：TN1096产 地：中国大陆
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TP1996MCH(human, mouse, rat)MCH(human, mouse, rat),inhibit,MCHR1 (GPR24),Inhibitor,Melanin concentrating h
Potent endogenous agonist at melanin-concentration hormone (MCH) receptors (IC50 values are 0.3 and 1.5 nM and EC50 values are 3.9 and 0.1 nM at MCH1 and MCH2 receptors respectively). Increases food intake in vivo.
价 格：￥电议型 号：TP1996产 地：中国大陆
