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Cas号索引 3
- 324769-06-4 | tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate (Catalog# : 91832)Coming soon!
- 33545-98-1 | tert-butyl N-(4-aminobutyl)carbamate,hydrochloride (Catalog# : 90105)Coming soon!
- 301673-16-5 | tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (Catalog# : 81824)Coming soon!
- 313657-42-0 | tert-butyl 3-methylpiperazine-1-carboxylate,hydrochloride (Catalog# : 81730)Coming soon!
- 393781-71-0 | Tert-butyl 2-ethylpiperazine-1-carboxylate (Catalog# : 81708)Coming soon!
- 359629-16-6 | tert-butyl 4-(aminomethyl)piperidine-1-carboxylate,hydrochloride (Catalog# : 81029)Coming soon!
- 312917-14-9 | TCS JNK 5a (Catalog# : 60202)TCS JNK 5a(JNK Inhibitor IX) is a selective inhibitor of JNK2 and JNK3 (pIC50 values
- 380315-80-0 | Tenovin-1 (Catalog# : 52529)Tenovin-1 is a inhibitor of SIRT1 and SIRT2; activator of p21 and p53.
- 393105-53-8 | Tiplaxtinin (Catalog# : 52218)Tiplaxtinin(PAI-039) is a selective and orally efficacious inhibitor of plasminogen a
- 329907-28-0 | TTP 22 (Catalog# : 52244)TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/
- 3039-71-2 | U-18666A (Catalog# : 20110401)U-18666A is an inhibitor of cholesterol synthesis. It acts by inhibiting desmosterol
- 314241-44-5 | UNC-669 (Catalog# : 178312)UNC-669是L3MBTL领域抑制剂。UNC669是专门针对 IC50 5μM的致死3恶性脑肿
- 383392-66-3 | UC-112 (Catalog# : 6111407)UC-112 is a novel potent IAP(Inhibitor of apoptosis) inhibitor; potently inhibit cell
- 312611-92-0 | VK-28 (Catalog# : 24154)VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
- 3034880-93-5 | VVD-130037 ( BAY-3605349 ) (Catalog# : 24110)VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
- 3008290-92-1 | XJTU-L453 (Catalog# : 24074)XJTU-L453 is a PI3Kα inhibitor with an IC50 value of 0.4 nM. XJTU-L453 can inhibit t
- 355406-09-6 | YM-155 hydrochloride (Catalog# : 6111414)YM155 is a potent survivin suppressant by inhibiting Survivin promoter activity with
- 371942-69-7 | YM-201636 (Catalog# : 121426)YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p110.
- 36341-25-0 | YL-109 (Catalog# : 110219)YL-109 has ability to inhibit breast cancer cell growth and invasiveness in vitro and
- 324077-30-7 | ZM 323881 hydrochloride (Catalog# : 122214) ZM323881 is a potent and selective inhibitor of VEGF-R2 tyrosine kinase in vitr
产品分类
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- ---- Epigenetic Reader Domain
- ---- Methionine Adenosyltransferase (MAT)
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- ---- JAK
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- ---- MEK
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- ---- JNK
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- ---- BCRP
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- ---- Na+/Ca2+ Exchanger
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- ---- GlyT1
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- ---- Proton Pump
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- ---- Monoamine Oxidase
- ---- IDO
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- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
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- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- -- Neuronal Signaling
- ---- COX
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- GABA Receptor
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- ---- Amyloid-β
- ---- 5-HT Receptor
- ---- γ-secretase
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- ---- NMDA Receptor
- ---- GlyT1
- ---- Beta-secretase
- ---- Sigma Receptor
- ---- mAChR
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- ---- Glucosylceramide Synthase (GCS)
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- ---- VEGFR
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- ---- FLT3
- ---- FGFR
- ---- c-Kit
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- ---- PI3K
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- ---- GSK-3
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最新产品
- 845959-55-9 | Mitoquinol mesylate (MitoQ) (Catalog# : 26A042)Mitoquinol mesylate (MitoQ) 是一种线粒体靶向抗氧化剂，具体而言，它
- 1246960-09-7 | SPG-601 ( VSN-16R ) (Catalog# : 24042)SPG-601（原名VSN-16R）是一种口服给药、同类首创的小分子药物，是
- 1421438-81-4 | LY3039478 ( Crenigacestat ) (Catalog# : 17021601)LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂，通过阻断 VEGFA/
- 72882-78-1 | PF-9366 (Catalog# : 184107)PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A)，肝外同种型。
- 2925330-18-1 | MAT2A-IN-22 (Catalog# : 26A021)MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
- | Pantothenate kinase-IN-3 (Catalog# : 26A041)泛酸激酶-IN-3（亦称化合物21，https://doi.org/10.1021/acs.jmedchem.5c03452）
- 2361124-03-8 | Claziprotamidum ( Claziprotamide ; BBP-671 ) (Catalog# : 26A040)Claziprotamidum（Claziprotamide；BBP-671）是一种强效、口服有效且能透过
- 2170608-85-0 | PZ-3022 (Catalog# : 26A039)PZ-3022是一种别构型的PanK激活剂，能够抵消C3-CoA的抑制作用。
- 2170608-82-7 | PZ-2891 (Catalog# : 193282)PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂，
- 902614-04-4 | Pantothenate kinase-IN-2 (Catalog# : 26A038)Pantothenate kinase-IN-2是一种泛酸激酶抑制剂，对PanK2的IC50值为92 nM，