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T7509PD 117519CI-947,PD-117519,Adenosine Receptor,Inhibitor,P1 receptor,PD117519,PD 117519,inhibit,CI 947
PD 117519 is an agonist of adenosine receptor
价 格：￥电议型 号：T7509产 地：中国大陆
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T7519RS-127445 hydrochlorideInhibitor,RS127445,5-HT Receptor,inhibit,RS-127445,RS127445 hydrochloride,Ser
RS 127445 is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist(pKi : 9.5).
价 格：￥电议型 号：T7519产 地：中国大陆
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T6205AT7519
AT7519 is a CDK1/2/4/6/9 inhibitor (IC50: 10-210 nM). It is less effective to CDK3 and little active to CDK7.
价 格：￥电议型 号：T6205产 地：中国大陆
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T1778AT7519 HydrochlorideAT7519 HCl；AT 7519 hydrochloride salt
AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9.
价 格：￥电议型 号：T1778产 地：中国大陆
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T12429PF-06751979PF-06751979
PF-06751979 is an inhibitor of β-site amyloid precursor protein cleaving enzyme 1 (BACE1) (IC50 of 7.3 nM in BACE1 binding assay).
价 格：￥电议型 号：T12429产 地：美洲
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T1778AT 7519 hydrochloride saltAT 7519 hydrochloride salt,AT7519 Hydrochloride,AT7519 HCl
AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9.
价 格：￥电议型 号：T1778产 地：美洲
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T6205AT7519AT7519
AT7519 is a CDK1/2/4/6/9 inhibitor (IC50: 10-210 nM). It is less effective to CDK3 and little active to CDK7.
价 格：￥电议型 号：T6205产 地：美洲
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T77519FC-116；化合物FC-116FC116；FC116
FC-116 is a potent Tubulin inhibitor with antitumour activity and inhibits tumour growth in mice. FC-116 induces apoptosis in colorectal cancer (CRC) cells and promotes protein degradation.
价 格：￥电议型 号：T77519产 地：中国大陆
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T751995-(2-Hydroxyethyl)-2’,3’-di-O-toluoyl-2’-deoxyuridine；化合物 5-(2-Hydroxyethyl)-2’,3’-di-O-toluoyl-2’-d
5-(2-Hydroxyethyl)-2´,3´-di-O-toluoyl-2´-deoxyuridine, a purine nucleoside analog, exhibits widespread antitumor activity specifically against indolent lymphoid malignancies. Its anticancer effects are primarily through the inhibition of DNA synthesis and the induction of apoptosis, among other mechanisms [1].
价 格：￥电议型 号：T75199产 地：中国大陆
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T751982’-O,4’-C-Methyleneadenosine 5’-monophosphate triethylammonium；化合物 2’-O,4’-C-Methyleneadenosine 5’-m
2’-O,4’-C-Methyleneadenosine 5’-monophosphate (triethylammonium), a purine nucleoside analog, exhibits wide-ranging antitumor activity against indolent lymphoid malignancies. Its anticancer mechanisms include inhibiting DNA synthesis and inducing apoptosis [1].
价 格：￥电议型 号：T75198产 地：中国大陆
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T751972’-Deoxy-2’-fluoroguanosine 5’-monophosphate triethyl ammonium；化合物 2’-Deoxy-2’-fluoroguanosine 5’-mo
2’-Deoxy-2’-fluoroguanosine 5’-monophosphate triethyl ammonium, a purine nucleoside analog, exhibits broad antitumor activity specifically targeting indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, among others [1].
价 格：￥电议型 号：T75197产 地：中国大陆
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T751962’-O-Methyladenosine 5’-monophosphate triethyl ammonium；化合物 2’-O-Methyladenosine 5’-monophosphate tr
2’-O-Methyladenosine 5’-monophosphate triethyl ammonium is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine , Clofarabine , Fludarabine phosphate and Vidarabine [1] .
价 格：￥电议型 号：T75196产 地：中国大陆
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T751952’-Deoxy-2’-fluoroadenosine 5’-monophosphate triethylammonium；化合物 2’-Deoxy-2’-fluoroadenosine 5’-mon
2’-Deoxy-2’-fluoroadenosine 5’-monophosphate (triethylammonium) is a purine nucleoside analog with extensive antitumor properties, particularly effective against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, among others [1].
价 格：￥电议型 号：T75195产 地：中国大陆
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T75194N4-(3,3,3-Trifluoropropanoyl)cytidine；化合物 N4-(3,3,3-Trifluoropropanoyl)cytidineN4-(3,3,3-Trifluoropr
N4-(3,3,3-Trifluoropropanoyl)cytidine, a cytidine analog, acts by inhibiting DNA methyltransferases (such as Zebularine0), exhibiting potential anti-metabolic and anti-tumor activities [1].
价 格：￥电议型 号：T75194产 地：中国大陆
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T751933’-Beta-C-Ethynyl-4-deoxyuridine；化合物 3’-Beta-C-Ethynyl-4-deoxyuridine3’-Beta-C-Ethynyl-4-deoxyuridin
3’-Beta-C-Ethynyl-4-deoxyuridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1] .
价 格：￥电议型 号：T75193产 地：中国大陆
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T751921-(b-D-Xylofuranosyl)-N6-(p-methoxybenzyl) adenine；化合物 1-(b-D-Xylofuranosyl)-N6-(p-methoxybenzyl) ad
1-(β-D-Xylofuranosyl)-N6-(p-methoxybenzyl) adenine, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, among others [1].
价 格：￥电议型 号：T75192产 地：中国大陆
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T751912’-O-(2-Methoxyethyl)guanosine 5’-triphosphate ammonium；化合物 2’-O-(2-Methoxyethyl)guanosine 5’-tripho
2’-O-(2-Methoxyethyl)guanosine 5’-triphosphate (ammonium), a purine nucleoside analog, exhibits extensive antitumor properties, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, among others [1].
价 格：￥电议型 号：T75191产 地：中国大陆
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T751905’-O-DMTr-2’,2’-difluoro-dC(Bz)-methyl phosphonamidite；化合物 5’-O-DMTr-2’,2’-difluoro-dC(Bz)-methyl ph
5’-O-DMTr-2’,2’-difluoro-dC(Bz)-methyl phosphonamidite is a purine nucleoside analog with extensive antitumor activity against indolent lymphoid malignancies. Its anticancer efficacy stems from the inhibition of DNA synthesis and the induction of apoptosis, among other mechanisms [1].
价 格：￥电议型 号：T75190产 地：中国大陆
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T7519RS-127445 hydrochloride；化合物RS 127445RS 127445|||MT 500；4-(4-氟-1-萘基)-6-(1-甲基乙基)-2-嘧啶胺盐酸盐|||RS 127445|
RS-127445 hydrochloride (MT 500) is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist(pKi : 9.5).
价 格：￥电议型 号：T7519产 地：中国大陆
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T7509PD 117519；(R)-N-(2,3-二氢-1H-茚基)腺苷CI947；CI947|||(R)-N-(2,3-二氢-1H-茚基)腺苷
PD 117519 (CI947) is an agonist of adenosine receptor
价 格：￥电议型 号：T7509产 地：中国大陆
