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T76667Z-Arg-SBzl；化合物 Z-Arg-SBzlZ-Arg-SBzl
Z-Arg-SBzl is a substrate of both bovine and activated human protein C [1] .
价 格：￥电议型 号：T76667产 地：中国大陆
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T76621Suc-Ala-Ala-Pro-Phe-SBzl；化合物 Suc-Ala-Ala-Pro-Phe-SBzlSuc-Ala-Ala-Pro-Phe-SBzl
Suc-Ala-Ala-Pro-Phe-SBzl serves as a substrate for rat intestinal mast cell protease (RMCP I), rat skeletal muscle mast cell protease (RMCP II), and Chymotrypsin. Additionally, it undergoes hydrolysis by glycine (R208G) [1] [2].
价 格：￥电议型 号：T76621产 地：中国大陆
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T7549Talnetant；化合物TalnetantSB 223412；SB 223412
Talnetant (SB 223412) is a selective, competitive, brain-penetrant NK3 receptor antagonist with the ability to modulate mesolimbic and mesocortical dopaminergic neurotransmission
价 格：￥电议型 号：T7549产 地：中国大陆
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T75361BSB；化合物 BSBBSB
BSB, a fluorescent probe derived from Congo red, binds to both extracellular amyloid β protein and various intracellular lesions characterized by abnormal tau and synuclein proteins. Acting as a prototype imaging agent for Alzheimer´s disease, BSB demonstrates versatility in detecting key pathological hallmarks of the condition [1].
价 格：￥电议型 号：T75361产 地：中国大陆
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T75255L1SB-435495 ditartrate；化合物 SB-435495 ditartrateSB-435495 ditartrate
SB-435495 ditartrate is a potent, selective, reversible, non-covalent, and orally active inhibitor of Lp-PLA2, demonstrating an IC50 value of 0.06 nM [1] [3].
价 格：￥电议型 号：T75255L1产 地：中国大陆
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T75255LSB-435495 hydrochloride；化合物 SB-435495 hydrochlorideSB-435495 hydrochloride
SB-435495 hydrochloride is a potent, selective, reversible, non-covalent, and orally active inhibitor of Lp-PLA2, exhibiting an IC50 of 0.06 nM [1] [3].
价 格：￥电议型 号：T75255L产 地：中国大陆
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T75255SB-435495；化合物 SB-435495SB-435495
SB-435495 is a compound characterized by its potent, selective, reversible, and non-covalent inhibition of Lp-PLA2, demonstrating an IC50 value of 0.06 nM. It is effective when administered orally.
价 格：￥电议型 号：T75255产 地：中国大陆
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T75013SB26019；化合物 SB26019SB26019
SB26019 is a potent anti-neuroinflammatory compound that modulates the activation of NF-κB by promoting the formation of monomeric α-tubulin. This action of SB26019, in turn, hinders the translocation of p65, signifying its regulatory effect on neuroinflammatory processes [1].
价 格：￥电议型 号：T75013产 地：中国大陆
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T7428SBI-115；化合物SBI-115SBI-115
SBI-115 is an antagonist of TGR5. SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5
价 格：￥电议型 号：T7428产 地：中国大陆
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T73935MsbA-IN-6；化合物 MsbA-IN-6MsbA-IN-6
MsbA-IN-6 is a potent antibiotic and inhibitor of the gram-negative ATP-binding cassette (ABC) transporter MsbA, an essential protein required for transporting lipopolysaccharide across the inner bacterial membrane. It exerts its bactericidal effect on Escherichia coli by inhibiting the ATPase and transport activity of MsbA, while retaining efficacy against multidrug-resistant clinical strains [1] [2].
价 格：￥电议型 号：T73935产 地：中国大陆
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T7365Inarigivir；化合物InarigivirORI-9020|||SB-9000；ORI-9020|||SB-9000
Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.
价 格：￥电议型 号：T7365产 地：中国大陆
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T73628PSB-12379 disodium；化合物 PSB-12379 disodiumPSB-12379 disodium
PSB-12379 disodium is a nucleotide analogue acting as a potent inhibitor of Ecto-5´-Nucleotidase (CD73), demonstrating inhibitory constants (Ki) of 9.03 nM in rats and 2.21 nM in humans [1] [2].
价 格：￥电议型 号：T73628产 地：中国大陆
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T73409SBI-993；化合物 SBI-993SBI-993
SBI-993, an analog of SBI-477, exhibits enhanced potency and possesses pharmacokinetic properties conducive to in vivo bioavailability. It promotes insulin signaling through the inhibition of the transcription factor MondoA.
价 格：￥电议型 号：T73409产 地：中国大陆
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T7277SB 242084；化合物SB 242084 dihydrochloride hydrateSB 242084 dihydrochloride hydrate；6 - 氯-2,3 - 二氢- 5 -甲
SB 242084 dihydrochloride hydrate is a psychoactive drug and research chemical which acts as a selective antagonist for the 5HT2C receptor.
价 格：￥电议型 号：T7277产 地：中国大陆
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T72578Siegesbeckialide I；化合物 Siegesbeckialide ISiegesbeckialide I
Siegesbeckialide I effectively suppresses LPS-induced NO production in RAW264.7 murine macrophages by directly interacting with IKKα/β.
价 格：￥电议型 号：T72578产 地：中国大陆
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T71950PSB-12054；化合物 PSB-12054PSB-12054
PSB-12054 is a potent P2X4 receptor inhibitor. PSB-12054 has IC(50) of 0.189 μM and good selectivity versus the other human P2X receptor subtypes.
价 格：￥电议型 号：T71950产 地：中国大陆
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T71093SB-1578 citrate；化合物 SB-1578 citrateSB-1578 citrate
SB-1578 citrate is a novel, orally bioavailable JAK2 inhibitor with specificity for JAK2 within the JAK family and also potent activity against FLT3 and c-Fms. SB1578 blocks the activation of these kinases and their downstream signaling in pertinent cells, leading to inhibition of pathological cellular responses. The biochemical and cellular activities of SB1578 translate into its high efficacy in two rodent models of arthritis.
价 格：￥电议型 号：T71093产 地：中国大陆
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T70771PSB-1737；化合物 PSB-1737PSB-1737
PSB-1737 is a Potent Agonists of the Orphan G Protein-Coupled Receptor GPR17 (EC50 270 nM).
价 格：￥电议型 号：T70771产 地：中国大陆
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T70466SB-201076；化合物 SB-201076SB-201076
SB-201076 is a potent ATP citrate-lyase inhibitor. SB-204990 is the prodrug of SB-201076.
价 格：￥电议型 号：T70466产 地：中国大陆
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