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T6958Prucalopride Succinateinhibit,5-HT Receptor,Inhibitor,Prucalopride Succinate,Serotonin Receptor,R108
Prucalopride is a selective, high affinity 5-HT4 receptor agonist, inhibiting human 5-HT(4a) and 5-HT(4b) receptor with Ki value of 2.5 nM and 8 nM, respectively.
价 格：￥电议型 号：T6958产 地：中国大陆
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T8958PU-H54inhibit,PUH54,PU-H54,Grp94,Inhibitor,PU-H-54,Hsp90α,HSP,Heat shock proteins,Grp94 inhibitor,Tr
PU-H54 is a purine-based inhibitor of Grp94. It is a Grp94-selective resorcinol-based inhibitor isolated through probing of the exclusive binding region of S2 subpocket in Grp94.
价 格：￥电议型 号：T8958产 地：中国大陆
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T8956BC-?1258LRR,F-box,inhibit,repeat,BC-?1258,BC ?1258,FBXL2,Apoptosis,tumor,Inhibitor,BC?1258
BC-1258 is a unique small molecule F-box/LRR-repeat protein 2 (FBXL2) activator.
价 格：￥电议型 号：T8956产 地：中国大陆
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TN6758PROPYL DISULFIDEPROPYL DISULFIDE
PROPYL DISULFIDE is a natural product.
价 格：￥电议型 号：TN6758产 地：中国大陆
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TP1886L1NoxA1ds acetate(1435893-78-9 free base)NoxA1ds acetate(1435893 78 9 free base),NoxA-1ds acetate(1435
NoxA1ds acetate is a potent and selective NADPH oxidase 1 (NOX1) inhibitor (IC50 : 20 nM). Exhibits selectivity for NOX1 over NOX2, NOX4, NOX5 and xanthine oxidase. Inhibits NOX1-derived O2- production in HT-29 human colon cancer cells. Attenuates VEGF-induced human pulmonary artery endothelial cell migration under hypoxic conditions in vitro.
价 格：￥电议型 号：TP1886L1产 地：中国大陆
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TN71582-(4-methoxyphenyl)-N-methyl-2-oxoacetamide
2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide is a marine derived natural products found in Polycarpa aurata.
价 格：￥电议型 号：TN7158产 地：中国大陆
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T15815LY3295668
LY3295668 is a selective inhibitor of Aurora A with Kis of 0.8 nM and 1038 nM for Aurora A and B, respectively.
价 格：￥电议型 号：T15815产 地：中国大陆
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T9845WAY-358871WAY 358871,WAY358871
Thrombin inhibitor 5 (compound 385) is a thrombin inhibitor with IC 50s ranging from 0.1 μM to 1 μM. Thrombin inhibitor 5 can be used for venous thromboembolism research[1].
价 格：￥电议型 号：T9845产 地：中国大陆
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T7104Dovitinib lactateFGFR,CHIR-258,Dovitinib,c-Kit,SCFR,PDGFR,CD117,Platelet-derived growth factor recep
Dovitinib lactate(TKI258) lactate is a potent inhibitor of fibroblast growth factor receptor 3 (FGFR3) (IC50 :5 nM).
价 格：￥电议型 号：T7104产 地：中国大陆
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TP2358KRPEP-2D acetateKRPEP2D acetate,KRPEP 2D acetate
KRPEP-2D acetate was identified as a K-Ras(G12D) selective inhibitory peptide against the G12D mutant of K-Ras, which is a key member of the Ras protein family and an attractive cancer therapeutic target.
价 格：￥电议型 号：TP2358产 地：中国大陆
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T16581Progabide
Progabide is an agonist of the gamma-aminobutyric acid receptor.
价 格：￥电议型 号：T16581产 地：中国大陆
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T14071A-385358Bcl-2 Family,A 385358,Inhibitor,A-385358,A385358,inhibit
A-385358 is a selective Bcl-xL inhibitor with Kis of 0.80 nM for Bcl-xL and 67 nM for Bcl-2, respectively.
价 格：￥电议型 号：T14071产 地：中国大陆
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TP1901L1Hemopressin (rat) acetate(568588-77-2 free base)Hemopressin (rat) acetate(568588772 free base),Hemop
Hemopressin (rat) acetate is a nonapeptide derived from the α1-chain of hemoglobin, is originally isolated from rat brain homogenates.?Hemopressin is orally active, selective and inverse agonist of CB2 cannabinoid receptors.?Hemopressin exerts antinociceptive action in inflammatory pain models.
价 格：￥电议型 号：TP1901L1产 地：中国大陆
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TN5894ToddanolToddanol
Toddanol is a coumarin extracted from the roots of Toddalia.
价 格：￥电议型 号：TN5894产 地：中国大陆
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T6148CX-6258 hydrochlorideCX6258 hydrochloride,Pim,CX6258,CX-6258,Pim kinases,4E-BP1,CX 6258 hydrochlorid
CX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
价 格：￥电议型 号：T6148产 地：中国大陆
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T7584zanubrutinibBtk,zanubrutinib,BGB3111,Inhibitor,inhibit,BGB 3111,Bruton tyrosine kinase
Zanubrutinib is an inhibitor of Bruton tyrosine kinase (BTK).
价 格：￥电议型 号：T7584产 地：中国大陆
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TN1858LeptomerineCholinesterase (ChE),acetyl,inhibit,Inhibitor,cholinesterase,Anticholinesterasic,Leptomer
Leptomerine is an alkaloid from stems of Esenbeckia leiocarpa Engl. (Rutaceae). Leptomerine shows as anticholinesterasic activity and can be used in Alzheimer Disease studies.
价 格：￥电议型 号：TN1858产 地：中国大陆
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TN5888Toddaculininhibit,Toddaculin,osteoclast,Inhibitor,differentiation,leukemic,Apoptosis,osteoblast,anti
Toddaculine may be beneficial for the prevention and treatment of osteoporosis, it can not only inhibit the differentiation of osteoclasts via activation of the NF-κB, ERK 1/2, and p38 MAPK signaling pathways, but can induce differentiation and mineralization of osteoblasts by regulating differentiation factors. Toddaculine also may serve as a pharmacological prototype for the development of novel anti-leukemic agents, it displays a dual effect as a cell differentiating agent and apoptosis induc
价 格：￥电议型 号：TN5888产 地：中国大陆
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T7586trifaroteneRAR/RXR,inhibit,trifarotene,CD-5789,Autophagy,RAR,Retinoid X receptors,acne,CD 5789,Retin
trifarotene is a potent and selective RARγ agonist with 65-fold and 16-fold selectivitiy for the RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM).
价 格：￥电议型 号：T7586产 地：中国大陆
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T6853GSK591GSK 591,EPZ-015866,GSK591,Inhibitor,GSK 3203591,EPZ 015866,inhibit,GSK-3203591,GSK-591,Histone
GSK591, Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).
价 格：￥电议型 号：T6853产 地：中国大陆
