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T5942Docosanoic acid二十二酸；Behenic Acid
Docosanoic acid is a long-chain saturated fatty acid. It has been found in peanut and M. oleifera seed oils.
价 格：￥电议型 号：T5942产 地：中国大陆
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T5941Anthraflavic acid2,6-二羟基蒽醌；2,6-Dihydroxyanthraquinone
Anthraflavic acid, a flavonoid, is a potent IQ mutagenicity and cytochrome P-448 inhibitor.
价 格：￥电议型 号：T5941产 地：中国大陆
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T5940Proxyphylline羟丙茶碱；7-(2-Hydroxypropyl)theophylline
Proxyphylline is a dual of adenosine A1/A2a receptor inhibitor and phosphodiesterase (PDE) inhibitor. Proxyphylline acts as a cardiac stimulant, vasodilator and bronchodilator.
价 格：￥电议型 号：T5940产 地：中国大陆
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T5633H3B-5942
H3B-5942 belongs to a class of ERα antagonists referred to as selective estrogen receptor covalent antagonists (SERCA).
价 格：￥电议型 号：T5633产 地：中国大陆
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T5594Cedrol
Cedrol is a cedrane sesquiterpenoid and a tertiary alcohol,Cedrol inhibits the cytochrome P450 (CYP) isoforms CYP2B6 and CYP3A4 (Kis = 0.9 and 3.4 μM, respectively)
价 格：￥电议型 号：T5594产 地：中国大陆
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T4594SR1078SR 1078
SR1078 is an agonist of retinoic acid receptor-related orphan receptor (ROR)α/γ.
价 格：￥电议型 号：T4594产 地：中国大陆
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T3720Tebanicline hydrochloride替巴克兰盐酸盐；Ebanicline hydrochloride；ABT-594 hydrochloride
Tebanicline (ABT-594, Ebanicline), is an effective synthetic nicotinic (non-opioid) analgesic drug.
价 格：￥电议型 号：T3720产 地：中国大陆
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T3015OlaparibAZD2281；KU0059436；奥拉帕尼
Olaparib is a small molecule inhibitor of PARP1/PARP2 (IC50: 5/1 nM) but is less effective against the PARP tankyrase-1 (IC50: 1.5 μM).
价 格：￥电议型 号：T3015产 地：中国大陆
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T25944PhenoxyacetoneNSC 1876；NSC-1876；NSC1876
Phenoxyacetone is an inhibitor of acetylcholinesterase.
价 格：￥电议型 号：T25944产 地：中国大陆
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T2594DextromilnacipranLevomilnacipran；左旋米那普仑
Levomilnacipran is a selective serotonin and norepinephrine reuptake inhibitor.
价 格：￥电议型 号：T2594产 地：中国大陆
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T2242Wnt-C594-(2-甲基-4-吡啶基)-N-[4-(3-吡啶基)苯基]苯乙酰胺；C59
Wnt-C59(C59) is a highly effective and specific Wnt signaling antagonis with PORCN enzymatic activity.
价 格：￥电议型 号：T2242产 地：中国大陆
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T19658EnfluraneNSC 115944；Efrane；NSC-115944；Ethrane；NSC115944；恩氟烷
Enflurane, a volatile anaesthetic, is a potent inhibitor of high conductance Ca2+-activated K+ channels of Chara australis. Enflurane is an internal standard in monitoring halogenated volatile anaesthetics by headspace gas chromatography-mass spectrometry
价 格：￥电议型 号：T19658产 地：中国大陆
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T17594Biotin-PEG8-acidBIOTIN-八聚乙二醇-丙酸
Biotin-PEG8-acid is a biotin-labeled, PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T17594产 地：中国大陆
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T15945MA-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 (D
价 格：￥电议型 号：T15945产 地：中国大陆
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T15942MK-7622M1 receptor modulator
MK-7622 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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T1594Vecuronium bromide维库溴铵；ORG NC 45
Vecuronium 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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T15594MKC8866
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
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
