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T22685CP-471474；化合物 T22685CP 471474；CP 471474
Broad spectrum MMP inhibitor (IC50 values are 0.7, 0.9, 13, 16 and 1170 nM for MMP-2, MMP-13, MMP-9, MMP-3 and MMP-1 respectively). Attenuates early left ventricular dilation after experimental myocardial infarction in mice.
价 格：￥电议型 号：T22685产 地：中国大陆
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T22684CP 339818 hydrochloride；化合物 T22684CP 339818 hydrochloride
KV1.3 channel antagonist
价 格：￥电议型 号：T22684产 地：中国大陆
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T22683CP-316819化合物 CP-316819CP 316819|||GPi 819
CP-316819 (GPi 819) is a potent inhibitor of glycogen phosphorylase (GPase) with hypoglycemic effects, inhibits huSMGPa and huLGPa, maintains neuronal activity during hypoglycemia, and can be used in the study of hyperglycemia.
价 格：￥电议型 号：T22683产 地：中国大陆
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T22681CP 135807；化合物 T22681CP 135807
CP 135807 is a 5-HT1D receptor agonist.
价 格：￥电议型 号：T22681产 地：中国大陆
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T22680CP-100356 hydrochloride；CP-100356 盐酸盐CP-100356 HCl|||CP 100356 hydrochloride；CP-100356 HCl|||CP 1003
CP-100356 hydrochloride is an orally active and low micromolar dual inhibitor of MDR1 (P-gp) and BCRP, a nucleotide-derived substrate analogue with inhibitory effects on MDR1-mediated Calcein-AM transporter and BCRP-mediated Prazosin transporter.CP-100356 Inhibits OATP1B1, induces stomatal opening in the dark.
价 格：￥电议型 号：T22680产 地：中国大陆
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T2268VER49009；化合物VER-49009CCT0129397|||VER 49009|||VER-49009；CCT0129397|||VER 49009|||VER-49009
VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).
价 格：￥电议型 号：T2268产 地：中国大陆
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T22268Benzyldimethylstearylammonium chloride十八烷基二甲基苄基氯化铵Benzyldimethylstearylammonium Chloride Hydrate|||十
Benzyl dimethyl stearyl ammonium chloride hydrate is a kind of mild smell chemical
价 格：￥电议型 号：T22268产 地：中国大陆
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T21268LSemax acetate(80714-61-0 free base)；化合物Semax acetateSemax acetate(80714-61-0 free base)
Semax acetate is a synthetic peptide analog of adrenocorticotropic hormone (ACTH) that has neuroprotective, analgesic, and anxiolytic properties.
价 格：￥电议型 号：T21268L产 地：中国大陆
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T21268Semax；化合物 T21268Semax
Semax is a synthetic peptide analog of adrenocorticotropic hormone (ACTH) that has neuroprotective, analgesic, and anxiolytic properties.
价 格：￥电议型 号：T21268产 地：中国大陆
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T21154Chlorfluazuron；化合物 T21154IKI 7899|||AI3-29785|||CCRIS 2680|||CGA 112913|||Atabron；IKI 7899|||AI3-297
Chlorfluazuron, a chitin synthesis inhibitor, is commonly used as an insect growth regulator for controlling the major insect pests in crops.
价 格：￥电议型 号：T21154产 地：中国大陆
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T19703LG100268化合物 T19703LG 100268|||LG-100268
LG100268 is an effective and selective rexinoid and retinoid-X receptor agonist. LG100268 binds to the α, β, and γ RXR receptors (IC50 = 3-4 nM).
价 格：￥电议型 号：T19703产 地：中国大陆
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T19653CPI-268456；化合物 T19653CPI-268456
CPI-268456 is a compound which has bioactive.
价 格：￥电议型 号：T19653产 地：中国大陆
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T19268D-Sedoheptulose 7-phosphate；化合物 T19268D-Sedoheptulose 7-phosphate
D-Sedoheptulose 7-phosphate is a common precursor of heptaic acid (group III) and hygromycin B (group IV) heptasaccharide. D-heptadecane 7-phosphate can be converted to NDP-heptose by similar biosynthetic pathways in these compounds.
价 格：￥电议型 号：T19268产 地：中国大陆
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T18268Mal-PEG1-Val-Cit-PABC-OH；化合物 T18268Mal-PEG1-Val-Cit-PABC-OH
Mal-PEG1-Val-Cit-PABC-OH is a 1 unit polyethylene glycol (PEG) ADC linker that possesses cleavable properties. This linker, commonly utilized in the synthesis of antibody-drug conjugates (ADCs), serves as a critical component facilitating the conjugation of drugs to antibodies[1].
价 格：￥电议型 号：T18268产 地：中国大陆
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T1769Pardoprunox；帕多芦诺SLV-308|||DU-126891；帕多芦诺|||SLV-308|||DU-126891
Pardoprunox (SLV-308) is a partial dopamine D2 agonist and noradrenergic agonist with serotonin 5-HT1A agonist properties. Pardoprunox has been used in trials studying the treatment of Early Stage Parkinson´s Disease and Advanced Stage Parkinson´s Disease.
价 格：￥电议型 号：T1769产 地：中国大陆
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T17268Y-26763化合物 T17268Y 26763|||Y26763
Y-26763 is a K+ channel opener and active metabolite of Y-27152. This is an ATP-sensitive K+ (KATP) channel activator.
价 格：￥电议型 号：T17268产 地：中国大陆
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T16851SB-267268；化合物 T16851SB-267268
SB-267268 inhibits human and mouse αvβ3 (IC50s: 0.68 and 0.29 nM, respectively). SB-267268 is a selective and nonpeptidic alpha(v)beta3 and alpha(v)beta5 integrins antagonist (Kis: 0.9, 0.5 and 0.7 nM for human αvβ3, monkey αvβ3 and human αvβ5, respectively).
价 格：￥电议型 号：T16851产 地：中国大陆
