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T37189BTCP maleate；BTCP maleateBTCP maleate
Preincubation of guinea pig brain membranes with BTCP was shown to produce an increase in the dissociation rate of [3H]TCP from PCP site。
价 格：￥电议型 号：T37189产 地：中国大陆
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T36189CAY10406CAY10406CAY10406|||CAY-10406
CAY10406 is a trifluoromethyl analog of an isatin sulfonamide compound that selectively inhibits caspases 3 and 7. The non-trifluoromethyl compound exhibits Ki values of 1.2 nM and 6 nM for caspases 3 and 7, respectively. For all of the other caspases tested, it is 100 to 1,000 times less potent. Caspases 3 and 7 are ´effector caspases´ that are downstream from the initiating steps of apoptosis, and are implicated in the main proteolytic processing of the apoptotic signal. No data is
价 格：￥电议型 号：T36189产 地：中国大陆
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T3561CPI1189；化合物CPI1189CPI-1189|||REN-1189|||CPI 1189；CPI-1189|||REN-1189|||CPI 1189
CPI1189 (REN-1189) is a TNF-a release inhibitor potentially for the treatment of sciatica and postherpetic neuralgia.
价 格：￥电议型 号：T3561产 地：中国大陆
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T35449α-(difluoromethyl)-DL-Arginine；2-(二氟甲基)精氨酸DFMA|||RMI 71897|||α-(difluoromethyl)-DL-Arginine；DFMA|||R
α-(difluoromethyl)-DL-Arginine (RMI 71897) is an enzyma-activated, irreversible inhibitor of arginine decarboxylase for E. coli (Ki = 800 μM), Pseudomonas aeruginosa, and Klebsiella pneumoniae. At 0.01 mM, it has been shown to prevent osmotic stress-induced increases in arginine decarboxylase activity and putrescine synthesis in oat leaf cells. When combined with a variety of polyamine analogues, α-(difluoromethyl)-DL-Arginine inhibited the growth of Trypanosoma Crui in mammalian host cells at a
价 格：￥电议型 号：T35449产 地：中国大陆
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T35348LDN-193189 2HCl乙磺普隆LDN-193189 2HCl|||DM-3189 2HCl
LDN-193189 2HCl (DM-3189 2HCl) is a selective BMP signaling inhibitor that inhibits ALK1,ALK2,ALK3 and ALK6, showing IC50s of 0.8 nM, 0.8 nM, 5.3 nM, and 16.7 nM, respectively, in kinase assays.LDN-193189 2HCl inhibited the transcriptional activity of BMP type I receptors in C2C12 cells, with IC50s of 5 nM and 30 nM, respectively. LDN-193189 2HCl inhibited the transcriptional activity of BMP type I receptors ALK2 and ALK3 in C2C12 cells, with IC50s of 5 nM and 30 nM, respectively, and was 200-fo
价 格：￥电议型 号：T35348产 地：中国大陆
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T35189XRD 489；化合物 T35189XRD489|||XRD-489|||D 489；XRD489|||XRD-489|||D 489
XRD 489 is a biochemical.
价 格：￥电议型 号：T35189产 地：中国大陆
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T34661SMDC818909；化合物 T34661SMDC 818909|||SMDC-818909；SMDC 818909|||SMDC-818909
SMDC818909 is an effective and selective p97 inhibitor.
价 格：￥电议型 号：T34661产 地：中国大陆
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T34409RS 1893；化合物 T34409RS-1893|||RS1893；RS-1893|||RS1893
RS 1893 is an orally active cardiotonic agent and its structure is different from that of cardiac glycosides and beta-stimulants.
价 格：￥电议型 号：T34409产 地：中国大陆
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T34286Remogliflozin etabonate；瑞格列净乙酸酯GSK189075|||GSK 189075|||GSK-189075A|||GSK189075A|||GSK-189075|||GSK
Remogliflozin etabonate (GSK189075A) is a prodrug of regaliflozin and an inhibitor SGLT2 with Ki values of 1.95, 2.14, 8.57, and 43.1μM for hSGLT2, rSGLT2, rSGLT1, and hSGLT1, respectively.
价 格：￥电议型 号：T34286产 地：中国大陆
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T34189PTZ-256；化合物 T34189phenothiazine derivative|||PTZ256；phenothiazine derivative|||PTZ256
PTZ-256 is a phenothiazine derivative with chemical name: 3-(10H-phenothiazin-10-yl)propane-1-amine. PTZ-256 has molecule weight 256, therefore, we call it as PTZ-256.
价 格：￥电议型 号：T34189产 地：中国大陆
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T33189m-Anisidine, 4-((5-p-tolylpentyl)oxy)-；化合物 T33189m-Anisidine, 4-((5-p-tolylpentyl)oxy)-
m-Anisidine, 4-((5-p-tolylpentyl)oxy)- is a Drug / Therapeutic Agent.
价 格：￥电议型 号：T33189产 地：中国大陆
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T3306PF-04418948；化合物PF04418948PF 04418948|||PF04418948；PF 04418948|||PF04418948
PF-04418948 is a potent EP2 receptor antagonist (IC50 = 16 nM for human EP2 receptors). Displays over 2000-fold selectivity for EP2 receptors over EP1, EP3, EP4, DP1 amd CRTH2 receptors; exhibits <30% binding at a diverse panel of GPCRs and ion channels at a concentration of 10 μM. Inhibits PGE2-induced increases in intracellular cAMP; reverses PGE2-invoked relaxation of mouse trachea (IC50 = 2.7 nM).
价 格：￥电议型 号：T3306产 地：中国大陆
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T32189Iproplatin；化合物 T32189JM-9|||CHIP|||Code name: JM9|||JM 9；JM-9|||CHIP|||Code name: JM9|||JM 9
Iproplatin is a synthetic second-generation platinum-containing compound related to cisplatin. Iproplatin binds to and forms DNA crosslinks and platinum-DNA adducts, resulting in DNA replication failure and cell death. Although less prone to glutathione inactivation compared to cisplatin, resistance to this agent has been observed in vitro due to repair of platination damage by tumor cells. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus)
价 格：￥电议型 号：T32189产 地：中国大陆
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T32134Icopezil maleate；化合物 T32134CP 118954-11|||CP-118,954-11；CP 118954-11|||CP-118,954-11
Icopezil maleate is a bio-active chemical.
价 格：￥电议型 号：T32134产 地：中国大陆
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T32037H 189；化合物 T32037H-189|||H189；H-189|||H189
H 189 is a decapeptide analog of human renin substrate with statine replacing leucine.
价 格：￥电议型 号：T32037产 地：中国大陆
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T31899FY26；化合物 T31899FY 26|||FY-26；FY 26|||FY-26
FY26 is a potent Os(II) anticancer drug candidate, exerts its activity by generating reactive oxygen species and disrupting the redox balance in cancer cells Coadministration of FY26 and nontoxic doses of L-BSO allows the potentiation of its anticancer activity, and most remarkably, it improves the selectivity for cancer cells versus normal fibroblasts.
价 格：￥电议型 号：T31899产 地：中国大陆
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T31898Fuzlocillin；化合物 T31898Fuzlocillinum|||Fuzlocilline；Fuzlocillinum|||Fuzlocilline
Fuzlocillin is a bio-active chemical. Detailed information has not been published.
价 格：￥电议型 号：T31898产 地：中国大陆
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T31896Furylfuramide；化合物 T31896NSC 44973；NSC 44973
Furylfuramide (also known as AF-2), a synthetic nitrofuran derivative, can be widely used as a food preservative in Japan.
价 格：￥电议型 号：T31896产 地：中国大陆
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T31895Furylacryloylglycylleucinamide；化合物 T31895NSC-334344|||Furylacryloylglycyl leucinamide|||Furylacryloy
furylacryloylglycyl leucinamide is a bioactive chemical.
价 格：￥电议型 号：T31895产 地：中国大陆
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T31894Furothiazole；化合物 T31894C 132|||NSC 523298|||C 132 (VAN)|||CCRIS 1194；C 132|||NSC 523298|||C 132 (VAN
Furothiazole is a bioactive chemical.
价 格：￥电议型 号：T31894产 地：中国大陆
