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T63603-deazaneplanocin A HCl；3-去氮腺嘌呤A盐酸盐3-deazaneplanocin A HCl
3-deazaneplanocin A HCl is both an S-adenosyl-l-homocysteine hydrolase inhibitor and an enhancer of zeste homolog 2(EZH2) inhibitor.
价 格：￥电议型 号：T6360产 地：中国大陆
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T63585HCV-IN-37；化合物 HCV-IN-37HCV-IN-37
HCV-IN-37 is a potent inhibitor of HCV. HCV-IN-37 is able to persist in rat plasma after oral administration to rats at a single dose of 15 mg/kg. The high potency of the active derivative HCV-IN-37 is mainly driven by the inhibition of the entry phase of the virus.
价 格：￥电议型 号：T63585产 地：中国大陆
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T63567HCV-IN-34；化合物 HCV-IN-34HCV-IN-34
HCV-IN-34 is an orally active HCV entry inhibitor. HCV-IN-35 exhibits good antiviral efficacy (EC50: 0.010 μM, CC50 (half of the maximum cytotoxic concentration): 7.50 μM).
价 格：￥电议型 号：T63567产 地：中国大陆
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T63566HCV-IN-33；化合物 HCV-IN-33HCV-IN-33
HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.
价 格：￥电议型 号：T63566产 地：中国大陆
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T6356(R)-Nepicastat HCl；盐酸内匹司他RS-25560-198 HCl；RS-25560-198 HCl|||盐酸内匹司他
(R)-Nepicastat HCl (RS-25560-198 HCl), the R-enantiomer of Nepicastat HCl, is a potent and selective inhibitor with IC50 of 25.1 nM and 18.3 nM for bovine and human dopamine-β-hydroxylase, with negligible affinity for twelve other enzymes and thirteen neurotransmitter receptors.
价 格：￥电议型 号：T6356产 地：中国大陆
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T63557hCA I-IN-1；化合物 hCA I-IN-1hCA I-IN-1
hCA I-IN-1 is a human carbonic anhydrase I (hCA I) inhibitor that acts on hCA I (Ki: 38.3 nM), hCA II (Ki: 716.4 nM), hCAIX (Ki: 940.1 nM) and hCAXII (Ki: 192.8 nM).
价 格：￥电议型 号：T63557产 地：中国大陆
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T63487AMG 925 HCl；化合物 AMG 925 HClAMG 925 HCl
AMG 925 HCl is a selective and potent dual inhibitor of FLT3 (IC50: 2±1 nM) and CDK4 (IC50: 3±1 nM).
价 格：￥电议型 号：T63487产 地：中国大陆
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T63467hCAII-IN-5；化合物 hCAII-IN-5hCAII-IN-5
hCAII-IN-5 (compound 12h) is a potent, selective inhibitor of human carbonic anhydrase II (hCA II) with an inhibition constant (IC50) of 4.55 ?M [1].
价 格：￥电议型 号：T63467产 地：中国大陆
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T6344Sevelamer hydrochloride；化合物Sevelamer HClSevelamer HCl；Sevelamer HCl
Sevelamer hydrochloride (Sevelamer HCl) is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.
价 格：￥电议型 号：T6344产 地：中国大陆
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T63407HCV-IN-36；化合物 HCV-IN-36HCV-IN-36
HCV-IN-36 is an orally active HCV entry inhibitor that exhibits good antiviral activity (EC50: 0.016 μM, CC50 (half of the maximum cytotoxic concentration): 8.78 μM).
价 格：￥电议型 号：T63407产 地：中国大陆
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T63406HCV-IN-35；化合物 HCV-IN-35HCV-IN-35
HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.
价 格：￥电议型 号：T63406产 地：中国大陆
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T63400hA2A/hCA XII modulator 1；化合物 hA2A/hCA XII modulator 1hA2A/hCA XII modulator 1
hA2A/hCA XII modulator 1 is a potent antagonist of the hA2A adenosine receptor (hA2AAR), a triazolopyrazine that acts on hA2AAR (Ki: 6.4 nM), hA1AR (Ki: 4.819 μM), and hA3AR (Ki>30 μM). hA2A/hCA XII modulator 1 Also a potent inhibitor of human carbonic anhydrase XII (hCA XII), capable of acting on hCA XII (Ki: 6.2 nM), hCA II (Ki: 46 nM), hCA IX (Ki: 466 nM) and hCA I (Ki: 8.351 μM). hA2A/hCA XII modulator 1 exhibits potential for cancer research.
价 格：￥电议型 号：T63400产 地：中国大陆
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T63399LmTOR/HDAC-IN-1 HCl；mTOR/HDAC抑制剂1盐酸盐mTOR/HDAC-IN-1 HCl（2815286-02-1 Free base)；mTOR/HDAC-IN-1 HCl（281
mTOR/HDAC-IN-1 HCl is a potent dual inhibitor of mTOR and HDAC with potential anti-inflammatory, anti-proliferative, autophagy and apoptosis-inducing effects for cancer research.
价 格：￥电议型 号：T63399L产 地：中国大陆
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T63396HCV-IN-38；化合物 HCV-IN-38HCV-IN-38
HCV-IN-38 is a selective, potent, orally active hepatitis C virus (HCV) inhibitor with an EC50 value of 15 nM and an SI value of 431. HCV-IN-38 has a good safety profile and oral pharmacokinetics, exhibiting high anti-HCV activity and low cytotoxic effects.
价 格：￥电议型 号：T63396产 地：中国大陆
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T63351LMS8511 HCl；MS8511盐酸盐MS8511 HCl(2866408-21-9 Free base)；MS8511 HCl(2866408-21-9 Free base)
MS8511 HCl is a selective and potent covalent inhibitor of G9a/GLP that acts by targeting cysteine residues in the substrate binding site. MS8511 has anticancer activity and antiproliferative activity and reduces intracellular H3K9me2 levels.MS8511 can be used to study a wide range of cancers including brain, breast, and ovarian cancers .
价 格：￥电议型 号：T63351L产 地：中国大陆
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T63276hCAXII-IN-4；化合物 hCAXII-IN-4hCAXII-IN-4
hCAXII-IN-4 is a selective and potent CA XII inhibitor with a Ki value of 6.4 nM for human CA XII.
价 格：￥电议型 号：T63276产 地：中国大陆
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T63158hCAIX-IN-10；化合物 hCAIX-IN-10hCAIX-IN-10
hCAIX-IN-10 (Compound 6i) is a selective inhibitor of carbonic anhydrase IX and XII, acting on hCA IX (Ki: 61.5 nM) and hCA XII (Ki: 586.8 nM). hCA IX and hCA XII are transmembrane isoforms of carbonic anhydrase that act as biomarkers for some types of tumours. hCA XII contributes to the maintenance of acid-base homeostasis in normal and tumour cells.
价 格：￥电议型 号：T63158产 地：中国大陆
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T63151IHCH-3064；化合物 IHCH-3064IHCH-3064
IHCH-3064 is a tumour immunotherapeutic agent that targets both the adenosine A2A receptor and HDAC. IHCH-3064 effectively binds A2AR (Ki: 2.2 nM) and selectively inhibits HDAC1 (IC50: 80.2 nM). Prexasertib Mesylate
价 格：￥电议型 号：T63151产 地：中国大陆
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T6310GW3965 hydrochloride；化合物GW3965 HClGW3965 HCl；GW3965 HCl
GW3965 hydrochloride (GW3965 HCl) is an effective and specific LXR agonist for hLXRα/β (EC50: 190/30 nM).
价 格：￥电议型 号：T6310产 地：中国大陆
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T62949(1R,3S)-THCCA-Asn；化合物 (1R,3S)-THCCA-Asn(1R,3S)-THCCA-Asn
(1R,3S)-THCCA-Asn (4j) is a selective inhibitor of thrombin (IC50: 0.07-0.14 μM) with anti-thrombotic effects.
价 格：￥电议型 号：T62949产 地：中国大陆
