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T22564Ambenonium dichloride；化合物 T22564Ambenonium dichloride
AChE inhibitor
价 格：￥电议型 号：T22564产 地：中国大陆
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T22562Altanserin hydrochloride化合物 T22562Altanserin hydrochloride
Altanserin hydrochloride is a 5-HT2A receptor antagonist.
价 格：￥电议型 号：T22562产 地：中国大陆
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T22560ALK5 Inhibitor II (hydrochloride)；化合物 T22560ALK5 Inhibitor II (hydrochloride)
ALK5 Inhibitor II is an ALK5 inhibitor. IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-β cellular assay, and ALK5 binding in HepG2 cells, respectively.
价 格：￥电议型 号：T22560产 地：中国大陆
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T2256CNX-1351化合物CNX13511-[4-[[2-(1H-吲唑-4-基)-4-(4-吗啉基)噻吩并[3,2-D]嘧啶-6-基]甲基]-1-哌嗪基]-6-甲基-5-庚烯-1,4-二酮
CNX-1351 is a potent and isoform-selective targeted covalent PI3Kα inhibitor.
价 格：￥电议型 号：T2256产 地：中国大陆
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T22456Voreloxin hydrochloride；化合物Voreloxin hydrochlorideSNS-595 hydrochloride|||Vosaroxin；SNS-595 hydrochl
Voreloxin hydrochloride (SNS-595 hydrochloride) is a potent inhibitor of Topoisomerase II with broad-spectrum anti-tumor activity.
价 格：￥电议型 号：T22456产 地：中国大陆
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T22387NSC 55655；化合物NSC556555-[(2-nitrophenyl)methylidene]thiazolidine-2,4-dione；5-[(2-nitrophenyl)methylid
NSC 55655 (5-[(2-Nitrophenyl)methylene]-2,4-thiazolidinedione) possesses antimicrobial and antioxidant activities and inhibits the proliferation of B. subtilis, S. aureus, K. pneumonia, E. coli, S. typhi , A. niger and C. albicans. A. niger and C. albicans, and can be used in diabetes mellitus.
价 格：￥电议型 号：T22387产 地：中国大陆
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T22385NSC 31156；化合物NSC 311565-[(3,4-dimethoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione；5-[(3,4-dimeth
NSC 31156 is a bioactive chemical.
价 格：￥电议型 号：T22385产 地：中国大陆
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T22356LLY-284化合物LLY-284LLY284|||LLY 284
LLY-284 is the diastereomer of LLY-283, which is a selective and potent SAM-competitive chemical probe for PRMT5. LLY-284 is much less active than LLY-283 and can be used as a negative control for LLY-283.
价 格：￥电议型 号：T22356产 地：中国大陆
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T22256c-Kit-IN-5-1；化合物AMG-253-(2-Aminoquinazolin-6-yl)-4-methyl-1-(4-(oxazol-2-yl)phenyl)pyridin-2(1H)-one
c-Kit-IN-5-1 (AMG-25) is a novel selective and potent c-Kit inhibitor.
价 格：￥电议型 号：T22256产 地：中国大陆
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T222505WKS；化合物5WKSZINC97756584；ZINC97756584
5WKS also known as ZINC97756584 is a biochemical. It is a G9a protein inhibitor.G9A/EHMT2 is a nuclear histone lysine methyltransferase that catalyzes H3K9me2, a reversible modification commonly associated with transcriptional gene silencing.5WKS can be used in the study of autoimmune diseases or tumors.
价 格：￥电议型 号：T22250产 地：中国大陆
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T2221Uridine；尿苷Uridin|||β-Uridine|||NSC 20256；Uridin|||β-Uridine|||NSC 20256|||尿苷
Uridine (Uridin), a nucleoside, consists of uracil and D-ribose by a β-N1-glycosidic bond.
价 格：￥电议型 号：T2221产 地：中国大陆
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T22192BMS 195614；化合物BMS 195614BMS614；BMS614
BMS 195614 (BMS614) is a selective RARα antagonist. BMS 195614 can bind to the RARα subunit.
价 格：￥电议型 号：T22192产 地：中国大陆
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T2204Diaveridine二氨藜芦啶二氨藜芦啶|||EGIS-5645|||敌菌净|||CCRIS-3784|||AI3-23935
Diaveridine (AI3-23935) (DVD) is a popular antibacterial synergist that is widely used in combination with sulfonamide. It has been reported to be genotoxic to mammalian cells, but more studies are required to clarify this.
价 格：￥电议型 号：T2204产 地：中国大陆
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T22009CB2 receptor agonist 2；CB2受体拮抗剂2ZINC72105556|||4-Quinolone-3-Carboxamide Furan CB2 Agonist；ZINC72105
CB2 receptor agonist 2 (ZINC72105556) is a potent and selective agonist for the CB2 (cannabinoid type 2) receptor, Ki = 8.5 nM. CB2 receptor agonist 2 has high affinity and selectivity for CB2.
价 格：￥电议型 号：T22009产 地：中国大陆
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T21957Guanabenz hydrochloride；化合物Guanabenz hydrochlorideNE56490；NE56490
Guanabenz hydrochloride (NE56490) is an orally active α2-adrenoceptor agonist with hypotensive effects.
价 格：￥电议型 号：T21957产 地：中国大陆
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T21956GSK3β inhibitor II；GSK3β 抑制剂IIGSK3β inhibitor II
GSK3β inhibitor II is a GSK3β inhibitor. GSK3β inhibitor II exhibits the research potential of Alzheimer´s disease (AD).
价 格：￥电议型 号：T21956产 地：中国大陆
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T21944LBIM 23056 Acetate；化合物BIM 23056 AcetateBIM 23056 Acetate (150155-61-6 Free base)；BIM 23056 Acetate (1
BIM 23056 Acetate is a??potent and surmountable human recombinant sst5 receptor antagonist.
价 格：￥电议型 号：T21944L产 地：中国大陆
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T21874CID 2745687；化合物CID 2745687CID 2745687
CID 2745687 is a GPR35 antagonist that inhibited the effects at human GPR35 of cromolyn disodium and zaprinast, two agonists that share an overlapping binding site.
价 格：￥电议型 号：T21874产 地：中国大陆
