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T70481,4-Naphthoquinone；1,4-萘醌α-Naphthoquinone|||Naphthalene-1,4-Dione|||P-Naphthoquinone|||para-naphthoq
1,4-Naphthoquinone (P-Naphthoquinone) was used as a potential inhibitor of monoamine oxidase and DNA topoisomerase activities[2]. It was also used to inhibit the acetyltransferase activity[1].
价 格：￥电议型 号：T7048产 地：中国大陆
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T70421,5-Isoquinolinediol；1,5-二羟基异喹啉1,5-Isoquinolinediol
1, 5-Isoquinolinediol is an inhibitor of poly(ADP-ribose) synthetase (PARP1; IC50: 0.39 μM). The poly(ADP-ribose) polymerases (PARPs) form a family of enzymes with roles in DNA repair and apoptosis. 1, 5-Isoquinolinediol has been used to study the role of PARP1 in both DNA repair and oxidant stress-induced cell death. This compound can be used with cells in culture and in animals.
价 格：￥电议型 号：T7042产 地：中国大陆
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T7035ANTHRAQUINONE-2-CARBOXYLIC ACID；蒽醌-2-羧酸ANTHRAQUINONE-2-CARBOXYLIC ACID
Anthraquinone-2-carboxylic acid acts as a potent anti-inflammatory and antinociceptive component in vivo, thus contributing to the immune regulatory role of fruits and herbs.
价 格：￥电议型 号：T7035产 地：中国大陆
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T70080Methasquin；化合物 MethasquinMethasquin
Methasquin is a folic acid antagonist that has been used in the treatment of experimental leukemia; acts by inhibiting the dihydrofolate reductase in the cell.
价 格：￥电议型 号：T70080产 地：中国大陆
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T7008Vacquinol-1；化合物Vacquinol-1Vacquinol 1；Vacquinol 1
Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death.
价 格：￥电议型 号：T7008产 地：中国大陆
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T6S1538Neochlorogenic acid；新绿原酸trans-5-O-Caffeoylquinic acid|||Neochlorogenate|||5-O-Caffeoylquinic acid；新绿
Neochlorogenic acid (trans-5-O-Caffeoylquinic acid) is an antioxidant compound used in the treatment of oxidative stress and related afflictions.
价 格：￥电议型 号：T6S1538产 地：中国大陆
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T6S1537Cryptochlorogenic acid；隐绿原酸4-O-Caffeoylquinic acid|||4-Caffeoylquinic acid；隐绿原酸|||4-O-Caffeoylquinic
1. Cryptochlorogenic acid (4-O-Caffeoylquinic acid) has antioxidant activity.
价 格：￥电议型 号：T6S1537产 地：中国大陆
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T6S15253,4-Dicaffeoylquinic acid；异绿原酸BIsochlorogenic acid B；Isochlorogenic acid B|||金银花|||异绿原酸B
3,4-Dicaffeoylquinic acid (Isochlorogenic acid B) has antioxidant activity.
价 格：￥电议型 号：T6S1525产 地：中国大陆
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T6964Resiquimod；雷西莫特R848|||S28463；R848|||雷西莫特|||S28463
Resiquimod (R848) is an imidazoquinoline amine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through the TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages, and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activation of other transcription factors. This may lead to an increase in mRNA levels and subsequent production of
价 格：￥电议型 号：T6964产 地：中国大陆
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T6954PRIMA-1化合物PRIMA-12,2-Bis(hydroxymethyl)-3-quinuclidinone|||NSC-281668|||PRIMA 1
PRIMA-1 (NSC-281668) is a mutant p53 reactivator. It induces apoptosis and inhibits growth of human tumors with mutant p53.
价 格：￥电议型 号：T6954产 地：中国大陆
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T69446Cochlioquinone A；化合物 Cochlioquinone ACochlioquinone A
Cochlioquinone A is an inhibitor of diacylglycerol kinase (DGK) and diacylglycerol acyltransferase (DGAT). It has been shown to reduce the concentration of phosphatidic acid in T cell lymphoma and has also been shown to compete with macrophage inflammatory protein-1α for binding to human CCR5 chemokine receptors.
价 格：￥电议型 号：T69446产 地：中国大陆
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T69320Aminoquinuride；化合物 AminoquinurideAminoquinuride
Aminoquinuride, also known as Surfen, is a proteoglycan binding agent that reduces inflammation but inhibits remyelination in murine models of Multiple Sclerosis. Murine T cell activation is regulated by Surfen.
价 格：￥电议型 号：T69320产 地：中国大陆
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T69279Mequitazine sulfoxide；化合物 Mequitazine sulfoxideMequitazine sulfoxide
Mequitazine sulfoxide is a potent histamine H1 antagonist or antihistamine.
价 格：￥电议型 号：T69279产 地：中国大陆
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T68896Daniquidone；达尼喹酮NSC 320846|||BAY-H 2049；NSC 320846|||BAY-H 2049
Daniquidone (Batracylin) is a potent dual inhibitor of DNA topoisomerase I and DNA topoisomerase II with cytotoxic and antiproliferative activity that induces DNA fragmentation for the study of neoplasms, immune disorders, and lymphatic disorders.
价 格：￥电议型 号：T68896产 地：中国大陆
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T68788Ellipticine quinone；化合物 Ellipticine quinoneEllipticine quinone
Ellipticine quinone, also known as NSC-383230, is a Drp1 inhibitor. rpitor1 and Drpitor1a inhibited the GTPase activity of Drp1 without inhibiting the GTPase of dynamin 1. Ellipticine quinone showed greater potency than the current std. Drp1 GTPase inhibitor, mdivi-?1, (IC50 for mitochondrial fragmentation are (0.06, and 10 μM, resp.)?. Ellipticine quinone suppressed lung cancer tumor growth in a mouse xenograft model. Ellipticine quinone also inhibited mitochondrial ROS prodn., prevented mi
价 格：￥电议型 号：T68788产 地：中国大陆
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T68694Quinacrine acetate；化合物 Quinacrine acetateQuinacrine acetate
Quinacrine acetate is a histamine N-methyltransferase inhibitor.
价 格：￥电议型 号：T68694产 地：中国大陆
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T68669Quinpirole；化合物 QuinpiroleQuinpirole
Quinpirole is a dopamine D2/D3 receptor agonist.
价 格：￥电议型 号：T68669产 地：中国大陆
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T68568Encequidar, HCl；化合物 Encequidar, HClEncequidar, HCl
Encequidar, also known as HM-30181, is an oral P-glycoprotein (P-gp) inhibitor developed to enhance the oral bioavailability of P-gp substrate drugs. Encequidar showed the highest potency (IC(50)=0.63nM) among several MDR1 inhibitors, including cycloporin A, XR9576, and GF120918, and effectively blocked transepithelial transport of paclitaxel in MDCK monolayers (IC(50)=35.4nM). Encequidar is currently under clinical trials.
价 格：￥电议型 号：T68568产 地：中国大陆
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T68483Quinagolide Free Base；化合物 Quinagolide Free BaseQuinagolide Free Base
Quinagolide Free Base is a non-ergot dopamine D(2)-agonist.
价 格：￥电议型 号：T68483产 地：中国大陆
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T68133quisultazine；化合物 quisultazinequisultazine
Quisultazine is a phenothiazine derivative with no central effects, can be classified as a non anti H2 antisecretory agent.
价 格：￥电议型 号：T68133产 地：中国大陆
