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T23746APA-H-MPO；化合物 T23746APAHMPO；APAHMPO
APA-H-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.
价 格：￥电议型 号：T23746产 地：中国大陆
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T23652AFD-21；化合物 T23652AFD21|||NS-2 Class 1 antiarrhythmic agent；AFD21|||NS-2 Class 1 antiarrhythmic agent
AFD-21 is a class I antiarrhythmic drug. It binds to sodium channels in their inactivated state and exerts use- and voltage-dependent inhibition of sodium channels with unbinding rates comparable to those of class I antiarrhythmic drugs with moderate kinetics.
价 格：￥电议型 号：T23652产 地：中国大陆
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T22661CHM-1；化合物CHM-1CHM-1
CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.
价 格：￥电议型 号：T22661产 地：中国大陆
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T2236RU 58841；化合物RU58841RU58841|||PSK-3841|||HMR-3841；4-[3-(4-羟基丁基)-4,4-二甲基-2,5-二氧代-1-咪唑烷基]-2-(三氟甲基)苯腈|||
RU 58841 (PSK-3841) is a specific androgen receptor antagonist or anti-androgen; RU 58841(PSK-3841) has a significant effect on hair regrowth.
价 格：￥电议型 号：T2236产 地：中国大陆
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T22067CHMFL-ABL-053；化合物 T22067CHMFL-ABL-053
CHMFL-ABL-053 (Compound 18a) is a potent, selective, and orally available BCR-ABL, SRC and p38 kinase inhibitor with IC 50 values of 70, 90 and 62 nM against ABL1, SRC and p38, respectively. CHMFL-ABL-053 is a potentially useful drug candidate for Chronic Myeloid Leukemia(CML)[1].
价 格：￥电议型 号：T22067产 地：中国大陆
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T21607Ataciguat；化合物AtaciguatHMR-1766；HMR-1766
Ataciguat (HMR-1766) (HMR-1766) is a potent and specific soluble guanylate cyclase (sGC) activator.
价 格：￥电议型 号：T21607产 地：中国大陆
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T21252DHMB；化合物DHMB2,3-Dihydroxy-4-Methoxybenzaldehyde；2,3-Dihydroxy-4-Methoxybenzaldehyde
DHMB (2,3-Dihydroxy-4-Methoxybenzaldehyde) exerts protective effects on intestinal epithelial cells. DHMB exhibits anti-inflammatory and antifungal capacity.
价 格：￥电议型 号：T21252产 地：中国大陆
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T19798Flurtamone；化合物 T19798Benchmark|||RE40885|||RE-40885|||RE 40885；Benchmark|||RE40885|||RE-40885|||RE 4
Flurtamone is an agricultural chemical. Flurtamone mainly used as an herbicide.
价 格：￥电议型 号：T19798产 地：中国大陆
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T18229m-PEG9-SH；化合物m-PEG9-SHm-PEG9-SH
m-PEG9-SH 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：T18229产 地：中国大陆
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T18226m-PEG9-CH2COOH；化合物m-PEG9-CH2COOHm-PEG9-CH2COOH
m-PEG9-CH2COOH is a PEG-based PROTAC linker. m-PEG9-CH2COOH can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T18226产 地：中国大陆
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T18184m-PEG3-SH化合物m-PEG3-SHM-PEG3-Thiol|||2-(2-(2-Methoxyethoxy)Ethoxy)Ethanethiol
m-PEG3-SH (M-PEG3-Thiol) is a PEG-based PROTAC linker. m-PEG3-SH can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T18184产 地：中国大陆
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T16570Pralnacasan；化合物 T16570VX-740|||HMR 3480；VX-740|||HMR 3480
Pralnacasan inhibits proinflammatory cytokines IL-18, IL-1β , and IFN-γ. Pralnacasan is an effective, non-peptide, and orally active interleukin-1β converting enzyme inhibitor (Ki: 1.4 nM). Pralnacasan has the potential for osteoarthritis and rheumatoid arthritis treatment.
价 格：￥电议型 号：T16570产 地：中国大陆
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T15487HMR 1556化合物 T15487HMR1556|||HMR 1556|||HMR-1556
HMR 1556 is a chromanol derivative and is an IKs blocker (IC50s of 10.5 nM and 34 nM in canine and guinea pig left ventricular myocytes, respectively).
价 格：￥电议型 号：T15487产 地：中国大陆
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T15480HG6-64-1；化合物 T15480HMSL 10017-101-1；HMSL 10017-101-1
HG6-64-1 is a potent and selective inhibitor of B-Raf (IC50: 0.09 μM on B-raf V600E transformed Ba/F3 cells).
价 格：￥电议型 号：T15480产 地：中国大陆
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T15159Dorzagliatin化合物DorzagliatinHMS5552
Dorzagliatin (HMS5552) is a dual-acting glucokinase (GK) activator. It also improves glycaemic control and pancreatic β-cell function in type 2 diabetes.
价 格：￥电议型 号：T15159产 地：中国大陆
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T14956CHMFL-BTK-01；化合物 T14956CHMFL-BTK-01
CHMFL-BTK-01 is an irreversible inhibitor of BTK (IC50: 7 nM) and also potently inhibits BTK Y223 auto-phosphorylation.
价 格：￥电议型 号：T14956产 地：中国大陆
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T13573Arrhythmias-Targeting Compound 1；化合物 T13573Arrhythmias-Targeting Compound 1
Arrhythmias-Targeting Compound 1 is a compound. It is used in the research of arrhythmias.
价 格：￥电议型 号：T13573产 地：中国大陆
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T13462(+)-DHMEQ；化合物 T13462(1R,2R,6R)-Dehydroxymethylepoxyquinomicin|||(1R,2R,6R)-DHMEQ；(1R,2R,6R)-Dehydrox
(+)-DHMEQ is an antioxidant transcription factor Nrf2 activator. (+)-DHMEQ is the enantiomer of (-)-DHMEQ.
价 格：￥电议型 号：T13462产 地：中国大陆
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T12902SHMT-IN-1；化合物SHMT-IN-1SHMT-IN-1
SHMT-IN-1 is a potent plasmodial serine hydroxymethyltransferase (SHMT) inhibitor with antitumor activity.
价 格：￥电议型 号：T12902产 地：中国大陆
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T125491Lehmbachol C；化合物 Lehmbachol CLehmbachol C
Lehmbachol C is a useful organic compound for research related to life sciences and the catalog number is T125491.
价 格：￥电议型 号：T125491产 地：中国大陆
