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T16529BEBT-908；化合物BEBT-908PI3Kα inhibitor 1|||MDK9521；PI3Kα inhibitor 1|||MDK9521
BEBT-908 (PI3Kα inhibitor 1) is a selective PI3Kα inhibitor (IC50 <0.1 μM). BEBT-908 also inhibits HDAC (0.1 μM≤IC50≤1 μM).
价 格：￥电议型 号：T16529产 地：中国大陆
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T16528PI-828；化合物PI-828LY 294002, 4gamma-NH2；LY 294002, 4gamma-NH2
PI-828 is a phosphatidylinositol 3-kinase (PI3K) inhibitor, which is widely used to study the physiological function of PI3K and also promotes stem cell differentiation into mesoderm.
价 格：￥电议型 号：T16528产 地：中国大陆
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T16527Phytic acid dodecasodium salt hydrate；植酸十二钠盐myo-Inositol, hexakis(dihydrogen phosphate) dodecasodium
Phytic acid dodecasodium salt hydrate (myo-Inositol, hexakis(dihydrogen phosphate) dodecasodium salt hydrate) is a phosphorus storage compound of seeds and cereal grains. Phytic acid dodecasodium salt hydrate inhibits the enzymatic superoxide source xanthine oxidase with an IC50 of 6 mM and has antioxidative, neuroprotective, and anti-inflammatory effects.
价 格：￥电议型 号：T16527产 地：中国大陆
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T16526Phorbol 12,13-dibutyrate；化合物 T16526PDBu|||Phorbol dibutyrate；PDBu|||Phorbol dibutyrate
Phorbol 12,13-dibutyrate is a PKC activator. It also is a potent skin tumor promoter.
价 格：￥电议型 号：T16526产 地：中国大陆
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T16525PhIP；化合物PhIPPhIP
PhIP is a heterocyclic aromatic amine (HAA) from cooked meat. It belongs to pyridine heterocyclic amine and is a 2B carcinogen with estrogen activity. PhIP forms adducts with DNA that promote cancer.
价 格：￥电议型 号：T16525产 地：中国大陆
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T16524Philanthotoxin 74 dihydrochloride；化合物Philanthotoxin 74 盐酸盐PhTx-74 HCl|||PhTx 74 dihydrochloride；PhTx
Philanthotoxin 74 dihydrochloride is an antagonist of AMPAR with IC50s of 263 and 296 nM for GluR3 and GluR1.
价 格：￥电议型 号：T16524产 地：中国大陆
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T16523LPhiKan 083；化合物PhiKan 083PhiKan 083
PhiKan 083 is a carbazole derivative
价 格：￥电议型 号：T16523L产 地：中国大陆
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T16523PhiKan 083 hydrochloride化合物 T16523PhiKan 083 hydrochloride
PhiKan 083 hydrochloride is a carbazole derivative. Which binds to the surface cavity and stabilizes Y220C (Kd: 167 μM). It also a relative binding affinity (Kd) of 150 μM in Ln229 cells.
价 格：￥电议型 号：T16523产 地：中国大陆
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T16522Phenoxodiol脱氢雌马酚脱氢雌马酚|||Dehydroequol|||Idronoxil|||Haginin E
Phenoxodiol (Idronoxil) activates the mitochondrial caspase system, inhibits X-linked inhibitor of apoptosis(XIAP), disrupts FLICE inhibitory protein(FLIP) expression, and sensitizes the cancer cells to Fas-mediated apoptosis. Phenoxodiol induces cell cycle arrest in the G1/S phase of the cell cycle and upregulates p21WAF1 via a p53 independent manner. Phenoxodiol also inhibits DNA topoisomerase II.
价 格：￥电议型 号：T16522产 地：中国大陆
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T16521Phenglutarimid；化合物 T16521Phenglutarimide|||Ciba 10870；Phenglutarimide|||Ciba 10870
Phenglutarimid is an anticholinergic. It is used as an antiparkinsonian agent.
价 格：￥电议型 号：T16521产 地：中国大陆
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T16520Ph-Bis(C1-N-(C2-NH-Boc)2)；化合物 T16520Ph-Bis(C1-N-(C2-NH-Boc)2)
Ph-Bis(C1-N-(C2-NH-Boc)2) is a versatile alkyl chain-derived linker employed in the synthesis of PROTACs[1].
价 格：￥电议型 号：T16520产 地：中国大陆
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T16519LBIM-46187 4HCl；化合物BIM-46187 4HClPH-064 4HCl；PH-064 4HCl
BIM-46187 4HCl (PH-064 4HCl) is a heterotrimeric G-protein complex inhibitor.
价 格：￥电议型 号：T16519L产 地：中国大陆
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T16519PH-064；化合物PH-064BIM-46187；BIM-46187
PH-064 (BIM-46187) is a heterotrimeric G-protein complex inhibitor.
价 格：￥电议型 号：T16519产 地：中国大陆
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T16518PH-002；化合物PH-002PH-002
PH-002, an inhibitor targeting the intramolecular domain interaction of apolipoprotein (apo) E4 in neuronal cells, additionally enhances mitochondrial motility and promotes neurite outgrowth, thereby countering related impairments.
价 格：￥电议型 号：T16518产 地：中国大陆
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T16517PGMI-004A；化合物PGMI-004APGMI-004A
PGMI-004A is an effective inhibitor of phosphoglycerate mutase 1 (IC50: 13.1 μM).
价 格：￥电议型 号：T16517产 地：中国大陆
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T16516PG01；化合物PG01Phenylglycine-01；Phenylglycine-01
PG01 is a potent CFTR Cl-channel potentiator, effective against ΔF508 (Ka 0.3 μM), and also against E193K, G970R and G551D (CFTR mutants), with Kd values of 0.22 μM, 0.45 μM and 1.94 μM, respectively.PG01 increases ΔF508-CFTR Cl- currents upon addition of forskolin. F508-CFTR Cl-current upon addition of Forskolin, correcting the gating defect of CFTR mutants.
价 格：￥电议型 号：T16516产 地：中国大陆
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T16515PF 750；化合物PF 750PF-750|||UNII-7756CPP14K|||ZINC27647189；PF-750|||UNII-7756CPP14K|||ZINC27647189
PF 750 (ZINC27647189) is a selective and covalent inhibitor of FAAH. PF 750 shows IC50s varying from 16.2 to 595 nM in different incubation times.
价 格：￥电议型 号：T16515产 地：中国大陆
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T16514PF 04531083；化合物PF 04531083PF 04531083
PF 04531083 is a selective blocker of the NaV1.8 channel. PF 04531083 can be used for neuropathic and inflammatory pain studies.
价 格：￥电议型 号：T16514产 地：中国大陆
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T16513PF 03709270；化合物 T16513ulopenem etzadroxil；ulopenem etzadroxil
PF 03709270 is an orally available ester prodrug form of sulopenem. It has broad-spectrum antibacterial activity against most gram-positive and gram-negative bacteria.
价 格：￥电议型 号：T16513产 地：中国大陆
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T16512PFE-360；化合物PFE-360PF-06685360；PF-06685360
PFE-360 (PF-06685360) is a potent and selective inhibitor of LRRK2 kinase (IC50: 2.3 nM in vivo).
价 格：￥电议型 号：T16512产 地：中国大陆
