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T82315GIV3727；化合物 GIV3727GIV3727
GIV3727, a bitter taste receptor hTAS2R antagonist, inhibits the activation of hTAS2R31 by saccharin and acesulfame potassium, effectively diminishing the bitter taste in foods, beverages, and pharmaceuticals [1].
价 格：￥电议型 号：T82315产 地：中国大陆
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T81315Raddeanoside R16；化合物 Raddeanoside R16Raddeanoside R16
Raddeanoside R16, an oleanane-type saponin, can be isolated from the rhizome of Anemone raddeana [1].
价 格：￥电议型 号：T81315产 地：中国大陆
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T80315Dermaseptin-S1；化合物 Dermaseptin-S1Dermaseptin-S1
Dermaseptin-S1, an antimicrobial peptide sourced from frog skin, exhibits efficacy against filamentous fungi [1].
价 格：￥电议型 号：T80315产 地：中国大陆
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T79315PROTAC TG2 degrader-2；化合物 PROTAC TG2 degrader-2PROTAC TG2 degrader-2
PROTAC TG2 degrader-2 (compound 7) is a selective competitive degrader of Transglutaminase 2 (TG2), exhibiting a dissociation constant (Kd) greater than 100 μM. It inhibits cell migration and reduces TG2 levels in ovarian cancer cells, making it a valuable tool for ovarian cancer research [1].
价 格：￥电议型 号：T79315产 地：中国大陆
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T78315Foravirumab；福拉韦单抗CR4098；CR4098
Foravirumab (CR4098) is a monoclonal antibody targeting antigenic site III of the rabies virus glycoprotein [1].
价 格：￥电议型 号：T78315产 地：中国大陆
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T76315HKPao；化合物 HKPaoHKPao
HKPao (Hunter-killer peptide ao) is a biologically active peptide with dual functionality, exhibiting anti-obesity and anti-tumor pro-apoptotic activities. It induces the release of cytochrome c from vesicles, thereby playing a significant role in cellular apoptosis [1].
价 格：￥电议型 号：T76315产 地：中国大陆
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T75315Phenacaine；化合物 PhenacainePhenacaine
Phenacaine (Holocaine), a local anesthetic, suppresses the calmodulin-dependent activation of erythrocyte Ca2+-ATPase and inhibits cyclic nucleotide phosphodiesterases in the brain and heart, as evidenced by studies [1] [2].
价 格：￥电议型 号：T75315产 地：中国大陆
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T7431516:0 EPC chloride；化合物 16:0 EPC chloride16:0 EPC chloride
16:0 EPC chloride, a saturated cationic lipid and a P-O-ethyl derivative, functions as a DNA and RNA transfecting agent. It is also utilized as a co-adjuvant in vaccine preparation and to enhance drug delivery [1].
价 格：￥电议型 号：T74315产 地：中国大陆
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T73371BAY-3153；化合物 BAY-3153BAY-3153
BAY-3153 is a selective CCR1 ( C-C motif chemokine receptor 1 ) antagonist (human IC 50 =3 nM ; rat IC 50 =11 nM ; mice IC 50 =81 nM) [1] .
价 格：￥电议型 号：T73371产 地：中国大陆
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T73315(S)-ZG197；化合物 (S)-ZG197(S)-ZG197
(S)-ZG197 is a compound that acts as a highly selective activator of the Staphylococcus aureus Caseinolytic Protease P (Sa ClpP), demonstrating efficacy at a concentration of 1.4 μM (EC50).
价 格：￥电议型 号：T73315产 地：中国大陆
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T73156LabMol-301；化合物 LabMol-301LabMol-301
LabMol-301, a chemical compound, effectively inhibits NS5 RdRp and NS2B-NS3pro activity with IC50 values of 0.8 μM and 7.4 μM, respectively. Additionally, it exhibits cytoprotective effects, safeguarding against Zika virus (ZIKV)-induced cell death.
价 格：￥电议型 号：T73156产 地：中国大陆
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T73155BMS-986339；化合物 BMS-986339BMS-986339
BMS-986339 is an orally active, potent FXR agonist that interacts via H-bond formation with the His298 and ASN287 residues. It is utilized in research focused on primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), and nonalcoholic steatohepatitis (NASH) for its anti-fibrosis properties.
价 格：￥电议型 号：T73155产 地：中国大陆
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T73154EGFR-IN-70；EGFR-IN-70EGFR-IN-70
EGFR-IN-70 is a potent EGFR inhibitor with IC 50 values of 23.6 and 307.5 nM for EGFR LR/TM/CS and EGFR WT , respectively. EGFR-IN-70 has anti-proliferative activity and suppresses phosphorylation of the EGFR . EGFR-IN-70 can be used for cancer research [1] .
价 格：￥电议型 号：T73154产 地：中国大陆
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T73153EGFR-IN-69；化合物 EGFR-IN-69EGFR-IN-69
EGFR-IN-69 is a potent inhibitor of the EGFR enzyme, demonstrating IC50 values of 4.3 nM for EGFR L858R/T790M/C797S, 6.6 nM for EGFR L858R/T790M, and 25.6 nM for EGFR 19del/T790M/C797S. This compound is utilized in the research of non-small-cell lung cancer (NSCLC).
价 格：￥电议型 号：T73153产 地：中国大陆
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T73152SLU-PP-915；化合物 SLU-PP-915SLU-PP-915
SLU-PP-915 is an agonist for Estrogen Related Receptors (ERR), exhibiting an EC50 value of roughly 400 nM across ERRα, ERRβ, and ERRγ. This compound shows promise for applications in enhancing oxidative metabolism and managing heart failure.
价 格：￥电议型 号：T73152产 地：中国大陆
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T73151USP22-IN-1；化合物USP22-IN-1USP22-IN-1
USP22-IN-1 is a ubiquitin-specific peptidase 22 (USP22) inhibitor that can be used to treat proliferative diseases or cancer.
价 格：￥电议型 号：T73151产 地：中国大陆
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T7315BAY1125976；化合物BAY1125976BAY1125976
BAY1125976 is an allosteric inhibitor of Akt1 and Akt2 (IC50s of 5.2 and 18 nM, respectively, in a time-resolved FRET assay)
价 格：￥电议型 号：T7315产 地：中国大陆
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T7295Miridesap；化合物MiridesapRo63-8695|||CPHPC|||GSK2315698；Ro63-8695|||CPHPC|||GSK2315698
Miridesap (GSK2315698) is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. It also produces significant reduction of SAP from cerebrospinal fluid and visceral amyloid deposits
价 格：￥电议型 号：T7295产 地：中国大陆
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T72315Caspase-3/7 activator 2；化合物 Caspase-3/7 activator 2Caspase-3/7 activator 2
Caspase-3/7 Activator 2 is a potent compound that selectively activates Caspase-3/7, demonstrating tumor specificity, anti-proliferative properties, and a high capacity for inducing apoptosis.
价 格：￥电议型 号：T72315产 地：中国大陆
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T71465IDP-73152；化合物 IDP-73152IDP-73152
IDP-73152 is a peptide deformylase inhibitor.
价 格：￥电议型 号：T71465产 地：中国大陆
