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T16594Propargyl-PEG10-amine；化合物 T16594Propargyl-PEG10-amine
Propargyl-PEG10-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T16594产 地：中国大陆
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T16427Padsevonil；帕塞沃尼UCB-0942|||UCB1415943-000；UCB-0942|||UCB1415943-000
Padsevonil (UCB-0942) is a potential GABA A receptor orthosteric modulator with antiepileptic activity for the treatment of epilepsy.
价 格：￥电议型 号：T16427产 地：中国大陆
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T15949Mahanimbine；马汉九里香碱Mahanimbine
Mahanimbine is found in the roots, leaves and stems of Murraya koenigii and is an orally active alkaloid extracted from Murraya koenigii. Bifidobacterium bifidum leaves on histopathological changes in pancreatic beta cells of streptozotocin-induced diabetic rats.
价 格：￥电议型 号：T15949产 地：中国大陆
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T15947MAC13243 HCl；化合物MAC13243 HClMAC13243 HCl
MAC13243 HCl, an inhibitor of LolA, a periplasmic chaperone that transports lipoproteins from the inner membrane to the outer membrane, is an antimicrobial agent with specificity and significant inhibitory effects on Gram-negative bacteria.
价 格：￥电议型 号：T15947产 地：中国大陆
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T15946MA-2029；化合物 T15946MA-2029
MA-2029 is selective for the motilin receptor over various other receptors and ion channels. MA-2029 is a selective and competitive motilin receptor antagonist (IC50=4.9 nM). MA-2029 may be useful for gastrointestinal disorders associated with disturbed gastrointestinal motility.
价 格：￥电议型 号：T15946产 地：中国大陆
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T15945MA-0204；化合物MA-0204MA-0204
MA-0204 is a highly selective and orally available peroxisome proliferator-activated receptor δ (PPARδ) modulator (EC50s: 0.4 nM, 7.9 nM and 10 nM for human, mouse and rat PPARδ, respectively). It is a potential treatment for Duchene Muscular Dystrophy (DMD).
价 格：￥电议型 号：T15945产 地：中国大陆
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T15944M77976；化合物M77976M77976
M77976 is a selective ATP-competitive inhibitor of pyruvate dehydrogenase kinase 4 (PDK4) with an inhibitory effect on PDK4, having an IC50 value of 648 μM. It is used for research related to obesity and diabetes.
价 格：￥电议型 号：T15944产 地：中国大陆
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T15943M443；化合物 M443M443
M443 is a potent small molecule inhibitor of MRK that inhibits radiation-induced activation of p38 and Chk2 and can be used in cancer research.
价 格：￥电议型 号：T15943产 地：中国大陆
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T15942MK-7622；化合物MK-7622M1 receptor modulator；M1 receptor modulator
MK-7622 (M1 receptor modulator) is a modulator of muscarinic M1 receptor positive allosteric.
价 格：￥电议型 号：T15942产 地：中国大陆
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T15940m-PEG9-Amine；化合物 T15940m-PEG9-Amine
m-PEG9-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15940产 地：中国大陆
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T1594Vecuronium bromide；维库溴铵ORG NC 45；ORG NC 45|||维库溴铵
Vecuronium bromide (ORG NC 45) is a synthetic, intermediate-acting mono-quaternary steroid and non-depolarizing neuromuscular blocking agent, with muscle relaxant activity.
价 格：￥电议型 号：T1594产 地：中国大陆
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T15673KU 59403；化合物 T15673KU 59403
KU 59403 is an effective ATM inhibitor (IC50: 3 nM, 9.1 μM, and 10 μM for ATM, DNA-PK, and PI3K, respectively).
价 格：￥电议型 号：T15673产 地：中国大陆
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T15594MKC8866；化合物MKC8866MKC8866
MKC8866 is a selective IRE1 RNase inhibitor (IC50: 0.29 μM in human vitro). MKC8866 inhibits IRE1 RNase in breast cancer cells leading to the decreased production of pro-tumorigenic factors and it can inhibit prostate cancer (PCa) tumor growth.
价 格：￥电议型 号：T15594产 地：中国大陆
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T14944CGS 15943；化合物CGS 15943CGS 15943
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
价 格：￥电议型 号：T14944产 地：中国大陆
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T14594Biotin-PEG3-NHS ester；化合物Biotin-PEG3-NHS esterBiotin-PEG3-NHS ester
Biotin-PEG3-NHS ester is a PROTAC linker based on the PEG structure and can be used to prepare PROTAC.
价 格：￥电议型 号：T14594产 地：中国大陆
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T14551Bevenopran；化合物BevenopranCB-5945|||ADL-5945；CB-5945|||ADL-5945
Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
价 格：￥电议型 号：T14551产 地：中国大陆
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T12869Sch59498；化合物 T12869Sch59498
Sch59498 is a potent phosphodiesterase 1c (Pde1c) inhibitor.
价 格：￥电议型 号：T12869产 地：中国大陆
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T1259497-[(7-Methoxy-3,7-dimethyl-2,5-octadienyl)oxy]-2H-；化合物 7-[(7-Methoxy-3,7-dimethyl-2,5-octadienyl)oxy
7-[(7-Methoxy-3,7-dimethyl-2,5-octadienyl)oxy]-2H- is a useful organic compound for research related to life sciences. The catalog number is T125949 and the CAS number is 1388140-07-5.
价 格：￥电议型 号：T125949产 地：中国大陆
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T125948Hymatoxin D；化合物 Hymatoxin DHymatoxin D
Hymatoxin D is a useful organic compound for research related to life sciences. The catalog number is T125948 and the CAS number is 138935-17-8.
价 格：￥电议型 号：T125948产 地：中国大陆
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T125947Amorphispironone；化合物 AmorphispirononeAmorphispironone
Amorphispironone is a useful organic compound for research related to life sciences. The catalog number is T125947 and the CAS number is 139006-28-3.
价 格：￥电议型 号：T125947产 地：中国大陆
