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产品数：86101
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T9777THP104cTHP-104c,Mitochondrial Metabolism,THP104c,inhibit,Inhibitor
THP104c is an inhibitor of mitochondrial fission.
价 格：￥电议型 号：T9777产 地：中国大陆
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T9768LNinerafaxstat trihydrochlorideNinerafaxstat trihydrochloride
Ninerafaxstat trihydrochloride shifts cellular metabolism to glucose oxidation from fatty acid oxidation. Ninerafaxstat trihydrochloride improves overall mitochondrial respiration and reduces fatty acid oxidation, thereby inhibiting the proliferation and growth of cancer cells.
价 格：￥电议型 号：T9768L产 地：中国大陆
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T97356-(4-methylpiperazin-1-yl)-4-o-tolylnicotinamide6(4methylpiperazin1yl)4otolylnicotinamide,6 (4 methy
6-(4-methylpiperazin-1-yl)-4-o-tolylnicotinamide can be used in the synthesis of befetupitant and netupitant.
价 格：￥电议型 号：T9735产 地：中国大陆
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TN12975-O-Methylvisamminolinhibit,Inhibitor,5 O Methylvisamminol,5OMethylvisamminol
5-O-Methylvisamminol is a natural product
价 格：￥电议型 号：TN1297产 地：中国大陆
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T9575MRTX9768SDMA,toxicity,glioblastoma,orally,MRTX9768,low,Inhibitor,hematological,MRTX-9768,MTAP,CDKN2A
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
价 格：￥电议型 号：T9575产 地：中国大陆
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T9766GW590735lipid,LDLc,GW-590735,GW 590735,HDLc,Peroxisome proliferator-activated receptors,GW590735,PPA
GW590735 is an effective and selective PPARα agonist with an EC50 of 4 nM on PPARα and at least 500-fold selectivity versus PPARδ and PPARγ. GW590735 can be used in dyslipidemia studies.
价 格：￥电议型 号：T9766产 地：中国大陆
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T9733PAL-4PAL-4,inhibit,PAL 4,LYPLAL1,Lysophospholipase-like 1,Metabolic disorders,Inhibitor,PAL4,1H1,2,4
PAL-4 stimulates the activity of LYPLAL1, a poorly characterized serine hydrolase with complex genetic links to human metabolic traits.
价 格：￥电议型 号：T9733产 地：中国大陆
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T9788SN32976SN-32976,SN32976
SN32976 is a pan PI3K inhibitor. SN32976 potently inhibited PI3K isoforms and mTOR, displaying preferential activity for PI3Kα and sparing of PI3Kδ.
价 格：￥电议型 号：T9788产 地：中国大陆
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T9497Niraparib tosylate monohyrateNiraparib tosylate,Apoptosis,cancer,MK-4827 tosylate,inhibit,breast,PAR
Niraparib, also know as MK-4827, is an inhibitor of poly (ADP-ribose) polymerase (PARP) with potential antineoplastic activity. MK4827 inhibits PARP activity, enhancing the accumulation of DNA strand breaks and promoting genomic instability and apoptosis. The PARP family of proteins detect and repair single strand DNA breaks by the base-excision repair (BER) pathway.
价 格：￥电议型 号：T9497产 地：中国大陆
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T7367Acumapimodinhibit,p38 MAPK,BCT197,BCT 197,Acumapimod,Inhibitor,Autophagy
Acumapimod is an orally active inhibitor of p38α MAPK (IC50 <1 μM).
价 格：￥电议型 号：T7367产 地：中国大陆
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T60007WAY-329764WAY329764,WAY 329764
WAY-329764 is an antibacterial agent (extracted from patent RU2371444 C1).
价 格：￥电议型 号：T60007产 地：中国大陆
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T7343PF-04979064Inhibitor,Phosphoinositide 3-kinase,Mammalian target of Rapamycin,PF 04979064,PF04979064,
PF-04979064 is a potent and selective PI3K and mTOR dual kinase inhibitor(Ki of 0.13 nM and 1.42 nM,respectively).
价 格：￥电议型 号：T7343产 地：中国大陆
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T98977-Methoxy-1-naphthaleneacetic acid7Methoxy1naphthaleneacetic acid,7 Methoxy 1 naphthaleneacetic acid
7-Methoxy-1-naphthaleneacetic acid is an inhibitor of auxin action in plants. 7-Methoxy-1-naphthaleneacetic acid inhibits polar auxin transport and tropic responses associated with asymmetric auxin distribution in Arabidopsis and maize. 7-Methoxy-1-naphthaleneacetic acid inhibits auxin transport mediated by AUX1, PIN, and ABCB proteins expressed in yeast.
价 格：￥电议型 号：T9897产 地：中国大陆
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T6611NSC697923
NSC697923 is a potent UBE2N (ubiquitin-conjugating enzyme E2 N, Ubc13) inhibitor. NSC697923 induces neuroblastoma (NB) cell death via promoting nuclear importation of p53 in p53 wild-type NB cells. NSC697923 also induces cell death in p53 mutant NB cells by activation of JNK-mediated apoptotic pathway. NSC697923 inhibits DNA damage and NF-κB signaling. Antitumor activity.
价 格：￥电议型 号：T6611产 地：中国大陆
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TP1973LOXA (17-33) acetateOXA (1733) acetate,OXA (17 33) acetate
OXA (17-33) acetate is a more potent agonist of orexin-1 receptor (OX1, EC50 = 8.29 nM)) over OX2 (EC50 = 187 nM).
价 格：￥电议型 号：TP1973L产 地：中国大陆
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T6515Go6976Go6976,Influenza Virus,arrest,inhibit,Go 6976,Protein kinase C,Go-6976,cell,PKC,Inhibitor
Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat brain), PKCα, and PKCβ1, respectively. Also a potent inhibitor of JAK2 and Flt3.
价 格：￥电议型 号：T6515产 地：中国大陆
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T17197UCL 2077UCL-2077,Inhibitor,UCL 2077,UCL2077,inhibit
UCL 2077 is a subtype-selective blocker of the epilepsy-associated KCNQ channels and it also is a selective slow-afterhyperpolarization channel blocker，with IC50 of 500 nM in hippocampal neurons in culture, having minimal effects on Ca2+ channels, action potentials, input resistance, and the medium afterhyperpolarization.
价 格：￥电议型 号：T17197产 地：中国大陆
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T6897Monomethyl auristatin ESGD1010,Microtubule/Tubulin,SGD 1010,Apoptosis,Monomethyl auristatin E,inhibi
Monomethyl auristatin E (MMAE), an antimitotic agent, inhibits cell division by blocking the polymerization of tubulin and also has inhibition of antibody-drug conjugates (ADCs) activity.
价 格：￥电议型 号：T6897产 地：中国大陆
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T23397ST 91ST 91
ST-91 is an agonist of α2-adrenoceptor with a mixed α-adrenergic receptor type/subtype selection profile.
价 格：￥电议型 号：T23397产 地：中国大陆
