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T83514(Z,Z)-3,13-Octadecadienyl acetate；化合物 (Z,Z)-3,13-Octadecadienyl acetate(Z,Z)-3,13-Octadecadienyl ace
(Z,Z)-3,13-Octadecadienyl acetate, extracted from the pheromone glands of female S. bicingulata moths, is crucial for attracting male counterparts and can be employed as bait to ensnare them [1].
价 格：￥电议型 号：T83514产 地：中国大陆
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T82514EAC3I；化合物 EAC3IEAC3I
EAC3I, an autocamtide-3 derived inhibitory peptide with the sequence KKALHRQEAVDAL, is a bioactive peptide that mimics the autoinhibitory region of the CaMKII regulatory domain (residues 278–290). It functions by competitively binding to the enzyme´s catalytic site.
价 格：￥电议型 号：T82514产 地：中国大陆
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T81514Peptide 5f；化合物 Peptide 5fPeptide 5f
Peptide 5f, sourced from wasp venom, exhibits antimicrobial properties effective against both bacterial and fungal pathogens, while demonstrating minimal hemolytic activity on human red blood cells [1].
价 格：￥电议型 号：T81514产 地：中国大陆
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T80514TAT-SAMβA；化合物 TAT-SAMβATAT-SAMβA
TAT-SAMβA, an RNAENFDRF (SAMβA) peptide conjugated to the TAT 47–57 protein-derived cell-penetrating peptide, acts as a selective antagonist of the Mfn1-βIIPKC association. It has been shown to protect mouse embryonic fibroblast cells (MEFs) from cytotoxicity induced by oxidative stress [1].
价 格：￥电议型 号：T80514产 地：中国大陆
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T79514ABCG2-IN-2；化合物 ABCG2-IN-2ABCG2-IN-2
ABCG2-IN-2 is a potent inhibitor of ABCG2, exhibiting favorable oral pharmacokinetic profiles in mice, and is applicable for investigating tumor multidrug resistance (MDR) and erythropoietic protoporphyria (EPP) [1].
价 格：￥电议型 号：T79514产 地：中国大陆
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T79272BDM91514；化合物 BDM91514BDM91514
BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E. coli BW25113 with an EC90 of 8 μM when coupled with 8 μg/mL Pyridomycin. Additionally, BDM91514 exhibits favorable plasma and microsomal stability [1].
价 格：￥电议型 号：T79272产 地：中国大陆
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T78514Timiperone；化合物 TimiperoneTimiperone
Timiperone exhibits a high affinity for cerebral dopamine D2 receptors, demonstrating antipsychotic activity as it mitigates stereotyped behavior. It is utilized in the research of schizophrenia [1] [2] [3].
价 格：￥电议型 号：T78514产 地：中国大陆
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T77625CCG-13514；化合物CCG-13514CCG-13514
CCG-13514 is a biochemical reagent to be developed for biosynthesis.
价 格：￥电议型 号：T77625产 地：中国大陆
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T775143-Chlorophenylboronic acid；3-氯苯硼酸3-Chlorophenylboronic acid
3-Chlorophenylboronic acid, a phenylboronic acid derivative, is an important intermediate in the synthesis of prolyl hydroxylase inhibitors, and can be used to synthesize a variety of compounds.The IC50 of 3-Chlorophenylboronic acid for lysophospholipase LYPLA2 was 0.418 ?M.
价 格：￥电议型 号：T77514产 地：中国大陆
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T76514HCV-1 e2 Protein (554-569)；化合物 HCV-1 e2 Protein (554-569)HCV-1 e2 Protein (554-569)
HCV-1 e2 Protein (554-569), a primary antigenic region within the Hepatitis C Virus envelope 2 (e2) protein, features a putative N-glycosylation site believed to impact the immune recognition of e2 [1].
价 格：￥电议型 号：T76514产 地：中国大陆
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T75514Blestrin D；化合物 Blestrin DBlestrin D
Blestrin D, a potent mixed-type butyrylcholinesterase (BChE) inhibitor with an IC50 value of 8.1 μM, is isolated from Bletilla striata and has applications in Alzheimer´s disease (AD) research [1].
价 格：￥电议型 号：T75514产 地：中国大陆
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T75149PROTAC BRD4 Degrader-19；化合物 PROTAC BRD4 Degrader-19PROTAC BRD4 Degrader-19
PROTAC BRD4 Degrader-19 (compound 176) is a proteolysis-targeting chimera (PROTAC) designed to specifically degrade the BRD4 protein, offering potential utility in cancer research [1].
价 格：￥电议型 号：T75149产 地：中国大陆
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T75148Hedgehog IN-3；化合物 Hedgehog IN-3Hedgehog IN-3
Hedgehog IN-3 (compound 3), with an IC50 value of 0.01 ?M, serves as a hedgehog pathway inhibitor, proving beneficial for cancer research applications [1].
价 格：￥电议型 号：T75148产 地：中国大陆
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T75147PCSK9-IN-18；化合物 PCSK9-IN-18PCSK9-IN-18
PCSK9-IN-18 (compound 188) is a potent PCSK9 inhibitor with a K D value of <200 nM [1] .
价 格：￥电议型 号：T75147产 地：中国大陆
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T75146KAT6-IN-1；化合物 KAT6-IN-1KAT6-IN-1
KAT6-IN-1 is a potent KAT6 inhibitor. KAT6-IN-1 can be used in research of cancer [1] .
价 格：￥电议型 号：T75146产 地：中国大陆
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T75145TRV-7019；化合物 TRV-7019TRV-7019
TRV-7019 is a butyrylcholinesterase-targeting radioligand capable of penetrating the blood-brain barrier (BBB) for brain imaging. It is utilized for diagnosing conditions such as amyloid diseases, multiple sclerosis, brain tumors, or to assess butyrylcholinesterase activity [1].
价 格：￥电议型 号：T75145产 地：中国大陆
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T75144WU-FA-01；化合物 WU-FA-01WU-FA-01
WU-FA-01, a hydrogenated derivative of WU-FA-00, functions as an antibacterial agent with robust activity against Gram-positive strains and possesses anti-inflammatory properties [1].
价 格：￥电议型 号：T75144产 地：中国大陆
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T75143Mcl-1 inhibitor 12；化合物 Mcl-1 inhibitor 12Mcl-1 inhibitor 12
Mcl-1 Inhibitor 12 (Example 10), with a K i of 0.22 nM, functions as an MCL-1 inhibitor. It is utilized in cancer research [1].
价 格：￥电议型 号：T75143产 地：中国大陆
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T75142Acid Ceramidase-IN-2；化合物 Acid Ceramidase-IN-2Acid Ceramidase-IN-2
Acid Ceramidase-IN-2 (compound 1), an acid ceramidase inhibitor, exhibits potentially antiproliferative and cytostatic effects. This compound is of interest due to the overexpression of human acid ceramidase in prostate cancer cells, suggesting its potential anti-tumor efficacy. Furthermore, the hydrolysis of Acid Ceramidase-IN-2 can be inhibited by 3 a-ketoamides: GT85, GT98, and GT99 in vitro [1].
价 格：￥电议型 号：T75142产 地：中国大陆
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T75141Aflatoxin Q1；化合物 Aflatoxin Q1Aflatoxin Q1
Aflatoxin Q1, a hydroxy metabolite of Aflatoxin B1 (AFB1)—a mycotoxin synthesized by Aspergillus flavus (A. flavus)—and aflatoxin B1 8,9-oxide are principal oxidative derivatives produced from Aflatoxin B1 in human liver microsomes across all substrate concentrations. The conversion of Aflatoxin B1 to Aflatoxin Q1 through 3 alpha-hydroxylation represents a critical detoxification route [1] [2].
价 格：￥电议型 号：T75141产 地：中国大陆
