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T76653Polybia-MP1；化合物 Polybia-MP1Polybia-MP1
Polybia-MP1 is an antimicrobial mastoparan peptide [1] .
价 格：￥电议型 号：T76653产 地：中国大陆
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T76652PHF6；化合物 PHF6PHF6
PHF6 (VQIVYK), a sequence within the third microtubule-binding repeat region of the tau protein, initiates the aggregation of the full-length tau protein through its self-assembly capabilities [1].
价 格：￥电议型 号：T76652产 地：中国大陆
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T76651Peptide YY (13-36) (canine, mouse, porcine, rat)；化合物 Peptide YY (13-36) (canine, mouse, porcine, rat
Peptide YY (13-36) (canine, mouse, porcine, rat) is a Y 2 receptor subtype agonist [1] .
价 格：￥电议型 号：T76651产 地：中国大陆
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T76650PAR-2 (1-6) (human)；化合物 PAR-2 (1-6) (human)PAR-2 (1-6) (human)
PAR-2 (1-6) (human) (SLIGKV), a peptide ligand, is a PAR-2 agonist [1] .
价 格：￥电议型 号：T76650产 地：中国大陆
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T7665[Leu5]-Enkephalin TFA(58822-25-6(free bas))化合物[Leu5]-Enkephalin TFALeu-enkephalin|||Leucine enkephal
[Leu5]-Enkephalin TFA(58822-25-6(free bas)) (Leucyl-enkephalin) is the most potent δ-receptor ago
价 格：￥电议型 号：T7665产 地：中国大陆
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T756653-O-Methylellagic acid；化合物 3-O-Methylellagic acid3-O-Methylellagic acid
3-O-Methylellagic acid, a natural product isolated from Myrciaria cauliflora, exhibits anti-inflammatory and antibacterial activities. This compound not only inhibits glucose transport but also demonstrates a minimum inhibitory concentration (MIC) of 32 μg/mL against Staphylococcus aureus ATCC 25923 [1] [2] [3].
价 格：￥电议型 号：T75665产 地：中国大陆
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T74665KTX-955；化合物 KTX-955KTX-955
KTX-955, a potent IRAK4 degrader, exhibits DC50 values of 5 nM for IRAK4 and 130 nM for Ikaros. It is primarily utilized in anticancer research [1] [2].
价 格：￥电议型 号：T74665产 地：中国大陆
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T73665Bufrolin；化合物 BufrolinBufrolin
Bufrolin, an analog of Cromoglycate (histamine release inhibitor) and a potent agonist of GPR35, enhances the interaction between β-arrestin-2 and both human GPR35a and rat GPR35. It stabilizes mast cells, exhibiting antiallergic properties, and inhibits anti-inflammatory responses triggered by internalization peptides. Furthermore, Bufrolin is researched for its anti-inflammatory properties in pharmaceutic applications associated with internalization peptides [1] [2] [3].
价 格：￥电议型 号：T73665产 地：中国大陆
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T73522CR 665；化合物 CR 665FE 200665|||JNJ 38488502 ; FE 200665|||JNJ 38488502；FE 200665|||JNJ 38488502 ; FE
CR 665 (JNJ 38488502) is a peripherally selective κ-opioid agonist, capable of activating the kappa opioid receptor with an EC50 value of 10.9 nM. It is utilized in the research of peripheral pain.
价 格：￥电议型 号：T73522产 地：中国大陆
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T72665P-gp inhibitor 3；化合物 P-gp inhibitor 3P-gp inhibitor 3
P-gp Inhibitor 3, an effective P-glycoprotein (P-gp) inhibitor, activates P-gp ATPase to inhibit P-gp´s efflux function. It demonstrates a relatively stronger multidrug resistance (MDR) reversal ability, thereby enhancing the anti-tumor efficacy of Paclitaxel.
价 格：￥电议型 号：T72665产 地：中国大陆
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T71665INCB-9471；化合物 INCB-9471INCB-9471
INCB-9471 is a CCR5 antagonist with anti-HIV activity and inhibits the interaction between HIV-1 gp120.
价 格：￥电议型 号：T71665产 地：中国大陆
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T71376Tzc 5665；化合物 Tzc 5665Tzc 5665
Tzc 5665 is a pyridazinone derivative with vasodilatory and beta-adrenergic blocking activities and type III phosphodiesterase inhibitory action.
价 格：￥电议型 号：T71376产 地：中国大陆
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T70875BI-665915；化合物 BI-665915BI-665915
BI-665915 is a 5-lipoxygenase activating protein inhibitor.
价 格：￥电议型 号：T70875产 地：中国大陆
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T70665PF-06284674；化合物 PF-06284674PF-06284674
PF-06284674 is a cell permeable, potent and selective M2 isoform of pyruvate kinase (PKM2) activator.
价 格：￥电议型 号：T70665产 地：中国大陆
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T70620VU0466551；化合物 VU0466551VU0466551
VU0466551 is a selective activator of homomeric G protein gated, inwardly rectifying, potassium subunit 1 (GIRK1) channels.
价 格：￥电议型 号：T70620产 地：中国大陆
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T70370PF-06658607；化合物 PF-06658607PF-06658607
PF-06658607 is an alkynylated irreversible Brutons tyrosine kinase (BTK) inhibitor.
价 格：￥电议型 号：T70370产 地：中国大陆
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T6S1665Irisflorentin；次野鸢尾黄素Irisflorentin
1. Irisflorentin blocks apoptosis pathways, by exerting its effects by promoting rpn-3 expression to enhance the activity of proteasomes and down-regulating egl-1 expression. 2. Irisflorentin has anti-inflammatory mechanism in LPS-activated RAW 264.7 macrophages, by reducing the transcriptional and translational levels of inducible nitric oxide synthase (iNOS) as well as the production of NO.
价 格：￥电议型 号：T6S1665产 地：中国大陆
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T6997SU6656；化合物SU6656SU6656
SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, 20 nM, 130 nM, and 170 nM for Src, Yes, Lyn, and Fyn, respectively.
价 格：￥电议型 号：T6997产 地：中国大陆
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T69665Zelasudil；化合物 ZelasudilRXC007；RXC007
Zelasudil (RXC007) is a Rho-related (ROCK) kinase inhibitor for the study of idiopathic pulmonary fibrosis and inflammation.
价 格：￥电议型 号：T69665产 地：中国大陆
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T68665Yonkenafil；化合物 Tunodafil (free base)Tunodafil；Tunodafil
Yonkenafil (Tunodafil), a novel phosphodiesterase 5 (PDE5) inhibitor, effectively reduces cerebral infarction, neurological deficits, edema, and neuronal damage in the infarcted area. It potentially enhances cognitive function through neurogenesis modulation and may have therapeutic effects on Alzheimer´s disease.
价 格：￥电议型 号：T68665产 地：中国大陆
