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T22697CS 2100；化合物CS 21001-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azeti
CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.
价 格：￥电议型 号：T22697产 地：中国大陆
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T22674Co 101244 hydrochloride；Co 101244盐酸盐4-Piperidinol, 1-[2-(4-hydroxyphenoxy)ethyl]-4-[(4-Methylphenyl)
Co 101244 hydrochloride (4-Piperidinol, 1-[2-(4-hydroxyphenoxy)ethyl]-4-[(4-Methylphenyl)Methyl]-,hydrochloride) is an NR2B-containing NMDA receptor antagonist.
价 格：￥电议型 号：T22674产 地：中国大陆
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T22636Phenyl-benzothiazole；2-(4-氨基苯基)-6-甲基苯并噻唑2-(p-Aminophenyl)-6-methylbenzothiazole|||4-(6-methyl-1,3-be
Phenyl-benzothiazole (2-(4-Aminophenyl)-6-methylbenzothiazole) is an azole for proteomics research.
价 格：￥电议型 号：T22636产 地：中国大陆
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T225195-bromo-3-phenyl Salicylic Acid化合物 T225195bromo3phenyl Salicylic Acid|||5 bromo 3 phenyl Salicylic A
AKR1C1 inhibitor
价 格：￥电议型 号：T22519产 地：中国大陆
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T225083-CPMT；化合物3-CPMTChlortropbenzyl hydrochloride|||3-[(4-chlorophenyl)-phenylmethoxy]-8-methyl-8-azabic
3-CPMT (FC-1) is a dopamine uptake inhibitor and a potent long-acting antihistaminic agent.
价 格：￥电议型 号：T22508产 地：中国大陆
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T22431SU5204；化合物SU52043-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one；3-[(2-Ethoxyphenyl)methylidene]-1H-in
SU5204 (3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one), an analogue of SU5025, pharmacologically inhibits VEGFR2(IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2)
价 格：￥电议型 号：T22431产 地：中国大陆
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T224241-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea；化合物SC-11-(4-Chloro-3-(triflu
SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib. SC-1 potently inhibits the phosphorylation of STAT3 by blocking STAT3 phosphorylation and activation, and induces apoptosis in hepatocellular carcinoma cell lines[1].
价 格：￥电议型 号：T22424产 地：中国大陆
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T22398Phenidone；菲尼酮1-phenyl-3-pyrazolidinone；菲尼酮|||1-phenyl-3-pyrazolidinone
Phenidone (1-phenyl-3-pyrazolidinone) is a dual inhibitor of cyclooxygenases and lipoxygenases that ameliorates rat paralysis in experimental autoimmune encephalomyelitis by suppressing its target enzymes[1]. The lipoxygenase inhibitor phenidone is a potent hypotensive agent in the spontaneously hypertensive rat[2].
价 格：￥电议型 号：T22398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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T22386NSC 31206；化合物NSC 312062,4-Thiazolidinedione,5-[(4-hydroxy-3-methoxyphenyl)methylene]-；2,4-Thiazolidi
NSC 31206 is a bioactive chemical.
价 格：￥电议型 号：T22386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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T22381Antimalarial agent 14；化合物 Antimalarial agent 144-hydroxy-3-phenyl-naphthalene-1,2-dione|||2-Hydroxy-
Antimalarial agent 14 (NSC-102533) is a bioactive chemical.
价 格：￥电议型 号：T22381产 地：中国大陆
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T22330Fenamic acid；N-苯基邻氨基苯甲酸2-Anilinobenzoic acid|||Diphenylamine-2-carboxylic acid|||2-(Phenylamino)benz
Fenamic acid (N-Phenylanthranilic acid) is a chloride channel blocker that causes renal papillary necrosis in rats. Fenamic acid serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including flufenamic acid, tolfenamic acid, mefenamic acid, and meclofenamic acid.
价 格：￥电议型 号：T22330产 地：中国大陆
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T22329Ethyl (triphenylphosphoranylidene) acetate乙氧甲酰基亚甲基三苯基膦Ethyl 2-(triphenylphosphoranylidene)acetate|||
Ethyl (triphenylphosphoranylidene) acetate ((Carbethoxymethylene)triphenylphosphorane) may act as an cholinesterase inhibitor that inhibits AChE and BChE.
价 格：￥电议型 号：T22329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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T22195CBFβ Inhibitor；5-乙基-4-(4-甲氧基苯基)-1,3-噻唑-2-胺5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine；5-乙基-4-(4-甲
CBFβ Inhibitor (5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine) is a cell-permeable CBFβ inhibitor and inhibits its association with Runx1.
价 格：￥电议型 号：T22195产 地：中国大陆
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T217034-Chlorophenylguanidine hydrochloride；洗必泰二乙酸杂质4-Chlorophenylguanidine hydrochloride
4-Chlorophenylguanidine hydrochloride is a potent inhibitor of urokinase selectivity. ?
价 格：￥电议型 号：T21703产 地：中国大陆
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T21667FAUC-365；化合物FAUC-365FAUC-365 Benzo[b]thiophene-2-carboxylic acid {4-[4-(2,3-dichloro-nphenyl)-piper
FAUC-365 is a D3 dopamine receptor agonist.
价 格：￥电议型 号：T21667产 地：中国大陆
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T21444Diphenylcyclopropenone二苯基环丙烯酮DPCP|||Diphencyprone|||二苯基环丙烯酮
Diphenylcyclopropenone (DPCP) is a topical drug used to treat alopecia areata, alopecia totalis, and refractory warts. Diphencyprone acts as a local stimulator that triggers an immune response against the action of autoreactive cells.
价 格：￥电议型 号：T21444产 地：中国大陆
