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T293492-Furamide, N-(5-(p-aminophenoxy)pentyl)-；化合物 T293492-Furamide, N-(5-(p-aminophenoxy)pentyl)-
2-Furamide, N-(5-(p-aminophenoxy)pentyl)- is a bioactive chemical.
价 格：￥电议型 号：T29349产 地：中国大陆
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T28517Renzapride hydrochloride；化合物 T28517BRL-24924|||ATL1251|||ATL-1251|||Renzapride HCl|||AZM-112；BRL-249
Renzapride is a 5-HT3 antagonist and 5-HT4 agonist. Renzapride also functions as a 5-HT2B antagonist and has some affinity for the 5-HT2A and 5-HT2C receptors.
价 格：￥电议型 号：T28517产 地：中国大陆
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T28492R-18893；化合物 T28492R18893；R18893
R-18893, a RNA-directed DNA polymerase inhibitor, is used potentially for the treatment of HIV-1 infection.
价 格：￥电议型 号：T28492产 地：中国大陆
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T28329PD 134922；化合物 T28329PD134922|||PD-134922；PD134922|||PD-134922
PD 134922 is a HIV-1 protease inhibitors. Inactivation of the protease prevents infectious virion formation.
价 格：￥电议型 号：T28329产 地：中国大陆
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T27878LY 164929；化合物 T27878LY-164929|||LY164929；LY-164929|||LY164929
LY 164929 is a highly selective ligand for the lower affinity [3H]D-Ala2-D-Leu-5-enkephalin binding site.
价 格：￥电议型 号：T27878产 地：中国大陆
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T27743KRH-594 free acid；化合物 T27743WK14922K|||WK-1492|||WK-14922K|||WK1492；WK14922K|||WK-1492|||WK-14922K||
KRH-594 is a potent, specific and insurmountable AT1 receptor antagonist. KRH-594 ameliorates hyperlipidaemia and nephropathy in diabetic spontaneously hypertensive rats. KRH-594 prevents end-organ damage in stroke-prone spontaneously hypertensive/Izm rats.
价 格：￥电议型 号：T27743产 地：中国大陆
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T27492GSK-8062；化合物 T27492GSK 8062；GSK 8062
GSK-8062 is an agonist of farnesoid X receptor (FXR).
价 格：￥电议型 号：T27492产 地：中国大陆
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T27379FR-194921；化合物 T27379FR194921；FR194921
FR-194921 is a potent, selective, and orally active antagonist for central adenosine A1 receptors with cognitive-enhancing and anxiolytic activity. FR194921 has same binding affinity profile among human, rat, and mouse.
价 格：￥电议型 号：T27379产 地：中国大陆
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T27219DuP-532；化合物 T27219DuP 532|||L 694492|||L694492|||L-694492；DuP 532|||L 694492|||L694492|||L-694492
DuP-532, an angiotensin type 1 receptor antagonist, is used potentially for the treatment of hypertension and heart failure.
价 格：￥电议型 号：T27219产 地：中国大陆
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T26897BRD2492；化合物BRD2492BRD2492
BRD2492 is a selective and potent dual inhibitor of HDAC1 and HDAC2 with potential anticancer, antitumour and antiproliferative activities, inhibiting HDAC1/2, HDAC3 and HDAC6.BRD2492 inhibits the growth of breast cancer cell lines and induces apoptosis.
价 格：￥电议型 号：T26897产 地：中国大陆
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T26146RU 24926；化合物 T26146RU-24926|||RU24926；RU-24926|||RU24926
RU 24926 is a di-(phenethyl)-amine derivative that used as a dopamine-D2 receptor agonist.
价 格：￥电议型 号：T26146产 地：中国大陆
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T26052RE 1492；化合物 T26052RE1492|||RE 1492|||RE 1492|||RE-1492|||RE1492|||RE-1492|||RE1492|||RE-1492；RE1492|
RE 1492 is an oligoamine that gives it an antiplatelet effect when combined with antithrombic drugs.
价 格：￥电议型 号：T26052产 地：中国大陆
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T25492Hepln-13；化合物Hepln-13Hepln 13|||Hepln13；Hepln 13|||Hepln13
Hepln-13 is a hepsin inhibitor that acts by hindering prostate cancer bone metastasis.
价 格：￥电议型 号：T25492产 地：中国大陆
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T24929V-06-018；化合物 T24929V 06 018；V 06 018
V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.
价 格：￥电议型 号：T24929产 地：中国大陆
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T24928UPR-IN-17#；化合物 T24928UPR inhibitor-17#|||UPR IN 17#|||UPR inhibitor 17#；UPR inhibitor-17#|||UPR IN 1
UPR-IN-17# is an effective pan-inhibitor of the unfolded protein response.
价 格：￥电议型 号：T24928产 地：中国大陆
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T24927Undecylprodigiosin；化合物 T24927Undecylprodigiosin
Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.
价 格：￥电议型 号：T24927产 地：中国大陆
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T24926UNC2327；化合物 T24926UNC-2327|||UNC 2327；UNC-2327|||UNC 2327
UNC2327 is a potent and selective inhibitor of protein arginine methyltransferase 3 (PRMT3) (IC50:230 nM).
价 格：￥电议型 号：T24926产 地：中国大陆
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T24925UNC-2170；化合物UNC-2170UNC2170 Maleate|||UNC-2170 Maleate|||UNC 2170 Maleate；UNC2170 Maleate|||UNC-2170
UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.
价 格：￥电议型 号：T24925产 地：中国大陆
