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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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T751895-Caroxy uracil-1-yl acetic acid benzyl ester；化合物 5-Caroxy uracil-1-yl acetic acid benzyl ester5-Car
5-Caroxy uracil-1-yl acetic acid benzyl ester, a purine nucleoside analog, exhibits broad antitumor activity primarily 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：T75189产 地：中国大陆
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T751882’-Deoxy-2’-fluorouridine 5’-monophosphate triethyl ammonium；化合物 2’-Deoxy-2’-fluorouridine 5’-monoph
2’-Deoxy-2’-fluorouridine 5’-monophosphate triethyl ammonium, a purine nucleoside analog, exhibits extensive antitumor effects against indolent lymphoid malignancies. Its anticancer mechanisms primarily involve the inhibition of DNA synthesis and the induction of apoptosis [1].
价 格：￥电议型 号：T75188产 地：中国大陆
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T751876-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine；化合物 6-Amino-4-hydrozi
6-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine, a pyrimidine nucleoside analog, boasts a broad spectrum of biochemical and anticancer activities, such as DNA and RNA synthesis inhibition, antiviral effects, and immunomodulatory properties [1].
价 格：￥电议型 号：T75187产 地：中国大陆
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T751865’-O-Benzoyl-3’-O-(4-methoxybenzyl)-2’-O,4’-C-methyleneuridine；化合物 5’-O-Benzoyl-3’-O-(4-methoxybenzy
5’-O-Benzoyl-3’-O-(4-methoxybenzyl)-2’-O,4’-C-methyleneuridine is a purine nucleoside analog with broad antitumor activity, primarily targeting indolent lymphoid malignancies. Its anticancer mechanisms include inhibiting DNA synthesis and inducing apoptosis, among others [1].
价 格：￥电议型 号：T75186产 地：中国大陆
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T751856-Amino-4-methoxy-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine；化合物 6-Amino-4-methoxy-1
6-Amino-4-methoxy-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine, a pyrimidine nucleoside analog, exhibits a broad spectrum of biochemical and anticancer activities. These activities encompass DNA synthesis inhibition, RNA synthesis inhibition, antiviral effects, and immunomodulatory effects [1].
价 格：￥电议型 号：T75185产 地：中国大陆
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T751844-Amino-5-cyano-1-(2-deoxy-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine；化合物 4-Amino-5-cyano-1-(2-d
4-Amino-5-cyano-1-(2-deoxy-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine, a pyrimidine nucleoside analog, exhibits a broad spectrum of biochemical and anticancer activities, encompassing DNA and RNA synthesis inhibition, antiviral effects, and immunomodulatory actions [1].
价 格：￥电议型 号：T75184产 地：中国大陆
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T751833,5’-Bis(O-t-butyldimethylsilyl)-2’-O-methyl-5-methyl cytidine；化合物 3,5’-Bis(O-t-butyldimethylsilyl)-
3,5’-Bis(O-t-butyldimethylsilyl)-2’-O-methyl-5-methyl cytidine, a cytidine analog, inhibits DNA methyltransferases (e.g., Zebularine), exhibiting potential anti-metabolic and anti-tumor activities [1].
价 格：￥电议型 号：T75183产 地：中国大陆
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T75182GK13S；化合物 GK13SGK13S
G13KS is a deubiquitinase UCHL1 ligand and inhibitor. G13KS inhibits recombinant and cellular UCHL1. G13KS reduces levels of monoubiquitin in human glioblastoma cells [1] .
价 格：￥电议型 号：T75182产 地：中国大陆
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T75181Antifungal agent 58；化合物 Antifungal agent 58Antifungal agent 58
Antifungal agent 58 (compound A21) exhibits high potency against Fluconazole-resistant strains and outperforms Miconazole in effectiveness. It inhibits Candida albicans strains with minimum inhibitory concentration (MIC) values ranging from 0.06 to 8 μg/mL [1].
价 格：￥电议型 号：T75181产 地：中国大陆
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T75180Antifungal agent 57；化合物 Antifungal agent 57Antifungal agent 57
Antifungal Agent 57 (Compound A19) demonstrates potent efficacy against Fluconazole-resistant strains, outperforming Miconazole. It effectively inhibits Candida albicans strains, exhibiting minimum inhibitory concentrations (MIC) ranging from 0.5 to 2 μg/mL [1].
价 格：￥电议型 号：T75180产 地：中国大陆
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T75179Antifungal agent 56；化合物 Antifungal agent 56Antifungal agent 56
Antifungal agent 56 (compound A09) is a potent antifungal agent, demonstrating superior efficacy against Fluconazole-resistant strains and outperforming Miconazole. It effectively inhibits Candida albicans strains, with minimal inhibitory concentration (MIC) values ranging from 0.03 to 0.25 μg/mL [1].
价 格：￥电议型 号：T75179产 地：中国大陆
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T75178Antifungal agent 55；化合物 Antifungal agent 55Antifungal agent 55
Antifungal agent 55 (Compound A07) effectively inhibits Fluconazole-resistant strains of Candida albicans, demonstrating greater efficacy than Miconazole. It exhibits minimum inhibitory concentrations (MIC) values ranging from 0.25-1 μg/mL [1].
价 格：￥电议型 号：T75178产 地：中国大陆
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T75177Antifungal agent 54；化合物 Antifungal agent 54Antifungal agent 54
Antifungal agent 54 (compound A05) serves as a potent inhibitor against Fluconazole-resistant strains, outperforming Miconazole in efficacy. It exhibits considerable activity against Candida albicans, with minimum inhibitory concentration (MIC) values ranging from 0.25-1 μg/mL [1].
价 格：￥电议型 号：T75177产 地：中国大陆
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T75176Antifungal agent 53；化合物 Antifungal agent 53Antifungal agent 53
Antifungal Agent 53 (A03), a potent Candida albicans CYP51 inhibitor, exhibits antifungal activity by preventing fungi biofilm formation and demonstrates good safety [1].
价 格：￥电议型 号：T75176产 地：中国大陆
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T75175JHDM-IN-1；化合物 JHDM-IN-1JHDM-IN-1
JHDM-IN-1 (Compound 1), a Jumonji C domain-containing HDMs (JHDM) inhibitor, exhibits IC50s of 3.4 μM against JMJD2C, 4.3 μM against JMJD2A, 5.9 μM against JMJD2E, 10 μM against PHF8, and 43 μM against JMJD3, showcasing its inhibitory effectiveness across a spectrum of JHDM enzymes [1].
价 格：￥电议型 号：T75175产 地：中国大陆
