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T6422Brimonidine TartrateBrimonidine Tartrate,AGN190342 (tartrate),UK 14304 (tartrate)
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：美洲
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T6423BRL-15572BRL-15572,BRL15572,BRL 15572
BRL-15572 is a 5-HT1D receptor antagonist with pKi of 7.9, also shows a considerable affinity at 5-HT1A and 5-HT2B receptors, exhibiting 60-fold selectivity over 5-HT1B receptor.
价 格：￥电议型 号：T6423产 地：美洲
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T6424Bromfenac SodiumBromfenac Sodium,AHR 10282R,Bronuck
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：美洲
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T6425BTZ043 RacemateBTZ043 Racemate,Benzothiazinone 10526038,BTZ10526038
BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2´-epimerase (DprE1) inhibitor, used as a new antimycobacterial agent.
价 格：￥电议型 号：T6425产 地：美洲
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T6426Buclizine HClBuclizine HCl,UCB-4445,Longifene
Buclizine HCl is the hydrochloride salt form of buclizine, a piperazine histamine H1 receptor antagonist with primarily antiemetic and antivertigo activities. Buclizine binds to and blocks the histamine H1 receptor, thereby preventing the symptoms that ar
价 格：￥电议型 号：T6426产 地：美洲
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T6427ButeinButein,2’,3,4,4’-tetrahydroxy Chalcone,
Butein, a plant polyphenol, is isolated from Rhus verniciflua. It can inhibit the activation of protein tyrosine kinase, NF-κB and STAT3, and also can inhibit EGFR.
价 格：￥电议型 号：T6427产 地：美洲
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T6428BV6BV6
BV6 is an antagonist of c-IAP1 and XIAP, members of the inhibitors of apoptosis (IAP) family.
价 格：￥电议型 号：T6428产 地：美洲
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T6429Caffeic Acid Phenethyl EsterCaffeic Acid Phenethyl Ester,CAPE,Phenylethyl Caffeate
Caffeic Acid Phenethyl Ester (CAPE) inhibits the activation of nuclear transcription factor NF-kappa B and may suppress p70S6K and Akt-driven signaling pathways, with antineoplastic, cytoprotective and immunomodulating activities. CAPE is the phenethyl al
价 格：￥电议型 号：T6429产 地：美洲
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T86424-CMTB；化合物4-CMTB4-CMTB
4-CMTB is a selective agonist of FFA2 and GPR43.It also is a positive allosteric modulator (pEC50=6.38).
价 格：￥电议型 号：T8642产 地：中国大陆
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T836423,3’-Selenobisalanine；化合物 3,3′-selenobis-L-Alanine dihydrochloride3,3′-selenobis-L-Alanine 2HCl|||3,
3,3´-Selenobisalanine is a derivative of amino acids.
价 格：￥电议型 号：T83642产 地：中国大陆
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T82642Cyclo(RGDfK(Mal))；化合物 Cyclo(RGDfK(Mal))Cyclo(RGDfK(Mal))
Cyclo(RGDfK(Mal)), a pentapeptide, enhances the attachment and infiltration of human pluripotent stem cells and is utilized in three-dimensional stem cell culture and expansion [1].
价 格：￥电议型 号：T82642产 地：中国大陆
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T81642NS2B-NS3pro-IN-1；化合物 NS2B-NS3pro-IN-1NS2B-NS3pro-IN-1
NS2B-NS3pro-IN-1, a potent Zika Virus NS2B-NS3 protease inhibitor, exhibits an EC50 of 50 μM and is significant in the ZIKV replication cycle [1].
价 格：￥电议型 号：T81642产 地：中国大陆
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T80642Foramsulfuron；化合物 ForamsulfuronForamsulfuron
Foramsulfuron, a postemergence sulfonylurea herbicide, selectively controls grass and certain broadleaved weeds in maize (Zea mays L.). It targets acetolactate synthase (ALS), an essential enzyme in the biosynthesis of branched chain amino acids, thus inhibiting weed growth [1].
价 格：￥电议型 号：T80642产 地：中国大陆
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T79642IV-275；化合物 IV-275IV-275
IV-275 is a dual inhibitor targeting the bromodomains of both BRG1 and BRM. This compound not only augments DNA damage when combined with Temozolomide and Bleomycin but also suppresses the invasiveness of GBM cells. Furthermore, IV-275 amplifies Temozolomide-induced cell death and its apoptosis-inducing activity [1].
价 格：￥电议型 号：T79642产 地：中国大陆
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T79019JNJ-64264681；化合物 JNJ-64264681JNJ-64264681
JNJ-64264681 is a potent, orally active, selective, and irreversible covalent inhibitor of Bruton´s tyrosine kinase (BTK). This compound demonstrates favorable pharmacokinetic properties and is applicable in the research of cancer and autoimmune diseases [1].
价 格：￥电议型 号：T79019产 地：中国大陆
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T78642Piperidine-4-sulfonic acid；4-哌啶磺酸Piperidine-4-sulfonic acid
Piperidine-4-sulfonic acid is a potent GABA agonist, demonstrating an IC50 value of 0.034 μM for the inhibition of H-GABA binding [1].
价 格：￥电议型 号：T78642产 地：中国大陆
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T776421-(aminomethyl)cyclopropanecarboxylic acid hydrochloride；1-(氨基甲基)环丙烷羧酸1-(aminomethyl)cyclopropanecar
1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride inhibits L amino acid transporter proteins and the α2δ subunit of voltage-gated calcium channels.1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride can be used as a biological module for the synthesis of active biochemical reagents.
价 格：￥电议型 号：T77642产 地：中国大陆
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T76642Acetyl-ACTH (2-24) (human, bovine, rat)；化合物 Acetyl-ACTH (2-24) (human, bovine, rat)Acetyl-ACTH (2-24
Acetyl-ACTH (2-24) (human, bovine, rat), a proopiomelanocortin (POMC) peptide fragment, includes adrenocorticotrophin (ACTH) precursor of α-MSH and acts as an agonist at the MC-1 receptor [1].
价 格：￥电议型 号：T76642产 地：中国大陆
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T76429Neurokinin Receptor (393-407), rat；化合物 Neurokinin Receptor (393-407), ratNeurokinin Receptor (393-40
Neurokinin Receptor (393-407), rat (SPR393–407), a fragment of the rat neurokinin 1 receptor (NK1R), undergoes rapid endocytosis and subsequent recycling to the plasma membrane upon substance P (SP) binding. This compound is instrumental in researching neurogenic inflammation [1] [2].
价 格：￥电议型 号：T76429产 地：中国大陆
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T76428(β-Ala8)-Neurokinin A (4-10)；化合物 (β-Ala8)-Neurokinin A (4-10)(β-Ala8)-Neurokinin A (4-10)
(β-Ala8)-Neurokinin A (4-10), a neuropeptide, acts as a potent and selective agonist for the NK-2 tachykinin receptor [1].
价 格：￥电议型 号：T76428产 地：中国大陆
