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36

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T21195	AICAR monophosphate Aica ribonucleotide,AICA riboside,Acadesine 5'-monophosphate,Z-nucleotide	Others	Others
	AICAR monophosphate (Aica ribonucleotide) 是一种具有抗肿瘤活性的嘌呤前体，可用于 2 型糖尿病的研究。
T9210	CD73-IN-4	CD73	Immunology/Inflammation
	CD73-IN-4 是高选择性的亚甲基膦酸 CD73抑制剂，对人 CD73 作用的 IC50值为 2.6 nM，在癌症免疫学中具有研究潜力。
T0297	Clofarabine Clofarex,氯法拉滨,克罗拉滨,Evoltra,Clolar	Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Autophagy	Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Clofarabine (Clofarex) 是一种核糖核苷酸还原酶抑制剂，IC50值为65 nM。它是核苷类似物，可用于癌症研究。
T14864	Caracemide NSC-253272,卡醋胺	Others; DNA/RNA Synthesis; Antibacterial	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others
	Caracemide (NSC-253272) 抑制大肠杆菌的核糖核苷酸还原酶。 Caracemide 可用于抗癌研究。
T3157	COH29 RNR Inhibitor COH29	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	COH29 (RNR Inhibitor COH29) 是一种口服可用的芳香族取代噻唑，是人类核糖核苷酸还原酶 (RNR) 的抑制剂，具有潜在的抗肿瘤活性。它抑制核糖核苷酸还原酶的IC50为 16 μM。
T8855	Polydeoxyribonucleotide(Sodium salt) Polydeoxyribonucleotide from salmon	Others	Others
	Polydeoxyribonucleotide(Sodium salt) 可改善大鼠跟腱损伤模型中各种生长因子的分泌，促进胶原蛋白合成，恢复跟腱的拉伸强度。
T0353	Osalmid Oxaphenamide,4'-Hydroxysalicylanilide,羟苯水杨胺,柳胺酚	HBV; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology
	Osalmid (Oxaphenamide) 是一种利胆药物，通过靶向核糖核苷酸还原酶小亚基 M2 来抑制核糖核苷酸还原酶的活性，IC50值为8.23 μM。
T8800	NSAH 2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	NSAH (2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide) 是一种可逆竞争性非核苷类的核苷酸还原酶抑制剂，无细胞 IC50 为 32 μM，基于细胞的 IC50 约为 250 nM。
T7525	Didox 3,4-二羟基苯甲羟肟酸,NSC-324360	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Didox (NSC-324360) 是一种合成的核糖核苷酸还原酶抑制剂，可降低患有痴呆症的 HIV 患者大脑中氧化损伤标志物的水平。
T1982	3-AP NSC663249,Triapine,PAN-811,OCX191	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	3-AP (Triapine) 是一种新型的核糖核苷酸还原酶 M2 亚基抑制剂，也是一种放射致敏剂。
T31163	Cytidine 5'-diphosphate disodium CDP sodium salt,Cytidine 5'-diphosphate disodium salt,胞苷-5'-二磷酸二钠盐,Cytidine diphosphate sodium salt	Others	Others
	Cytidine 5'-diphosphate disodium (CDP sodium salt) 产生 CTP 以支持 DNA 和 RNA 生物合成和核糖核苷酸还原酶以产生 dCMP。
T15826	Lometrexol LY 264618,DDATHF	DHFR	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism
	Lometrexol (LY 264618) 是一种抗嘌呤类抗叶酸 (Antifolate) 药，可抑制甘氨酰胺核糖核苷酸甲酰基转移酶 (GARFT) 的活性，但不会引起可检测水平的 DNA 链断裂。Lometrexol 可以进一步抑制嘌呤从头合成，导致异常的细胞增殖，凋亡 (Apoptosis) 和细胞周期停滞。Lometrexol 具有抗癌活性。Lometrexol 还是一种有效的人丝氨酸羟甲基转移酶 1/2 (hSHMT1/2) 抑制剂。
T6501	Fludarabine Phosphate NSC 312887 Phosphate,fludara Phosphate,F-ara-A (NSC 312887) Phosphate,F-ara-AMP,磷酸氟达拉滨	Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Fludarabine Phosphate (NSC 312887 Phosphate) 是一种腺苷和脱氧腺苷类似物，与 dATP 竞争，并入到 DNA，可以抑制 DNA 聚合酶 α、核糖核苷酸还原酶和 DNA 引发酶，从而中断 DNA 合成并抑制肿瘤细胞生长。
T14147	Pelitrexol AG 2037	DHFR	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism
	Pelitrexol (AG 2037) is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor.
T68230	Amidox
	Amidox is a ribonucleotide reductase inhibitor.
T11921	LY 222306	DHFR	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism
	LY 222306 is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor with a Ki of 0.77 nM.
T29197	YZ51
	YZ51, a novel potent inhibitor of ribonucleotide reductase (RR), inhibits hepatitis B virus replication by targeting ribonucleotide reductase M2 protein.
T24980	5-DACTHF 543U76,5-Deazacyclotetrahydrofolate
	5-DACTHF is an inhibitor of glycinamide ribonucleotide transformylase and aminoimidazole ribonucleotide transformylase used as an anti-purine drug.
T26572	AG2034 AG-2034,AG 2034
	AG2034 is an inhibitor of the glycinamide ribonucleotide formyltransferase (GARFT).
T15813	LY309887	LTR	Immunology/Inflammation
	LY309887 is a potent inhibitor of glycinamide ribonucleotide formyltransferase (Ki: 6.5 nM). It also has antitumor activity.
TNU0230	2’-Azido-2’-deoxycytidine
	Nucleoside Derivatives - Azido-nucleosides, 2’-Modified nucleosides; Drugs and Inhibitors; antiviral agent, DNA synthesis inhibitor; Ribonucleotide reductase inhibitor
T10068	2'-Azido-2'-deoxyuridine N3dUrd	Others	Others
	2'-Azido-2'-deoxyuridine (N3dUrd) is a ribonucleotide reductase inhibitor with anti-cancer activity.
T11884	LSN 3213128	Others	Others
	LSN 3213128, anti-tumor activity. is a selective, nonclassical, orally bioavailable antifolate with potent and specific inhibitory activity for aminoimidazole-4-carboxamide ribonucleotide formyltransferase (AICARFT), with IC50 of 16 nM for AICARFT enzyme inhibiton and 19 nM in cells.
T82950	ATIC-IN-1
	ATIC-IN-1 (compound 14) 是一种针对ATIC二聚体化的抑制剂，具有Ki值685 nM。ATIC二聚体形成对AICAR转化酶功能是必要的。ATIC-IN-1展现了通过减少细胞数和降低细胞分裂率的抗肿瘤活性。
T40862	Fludarabine triphosphate 三磷酸氟达拉滨,F-ara-ATP
	Fludarabine triphosphate (F-ara-ATP), the cytotoxic metabolite of Fludarabine phosphate , inhibits ribonucleotide reductase and DNA polymerase and ultimately leads to cellular apoptosis.
TNU0133	3’-Azido-3’-deoxycytidine
	Nucleoside Derivatives –Azido-nucleosides, 3’-Modified nucleosides; Drugs and Inhibitors; Ribonucleotide reductase inhibitor
T78814	COH1	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	COH1为核糖核苷酸还原酶(RR)抑制剂，主要应用于癌症、线粒体疾病和神经退行性疾病的研究领域。
T36300	Uridine-5’-monophosphate (sodium salt hydrate)
	Uridine-5’-monophosphate (UMP) is a ribonucleotide.1It is formedviadecarboxylation of orotidine-5’-monophosphate (5’-OMP) by OMP decarboxylase. UMP is further phosphorylated by UMP-CMP kinase to form UDP and UTP during nucleic acid biosynthesis. Formulations containing UMP have been used as dietary supplements. 1.Berg, J.M., Tymoczko, J.L., and Stryer, L.Nucleotide BiosynthesisBiochemistry(2002)
T76517	Herpes virus inhibitor 2
	Herpes virus inhibitor 2 为一种疱疹病毒抑制剂，专门破坏疱疹病毒的核糖核苷酸还原酶四级结构，从而抑制病毒复制。
T76515	Herpes virus inhibitor 1
	Herpes virus inhibitor 1 是一种抑制疱疹病毒的化合物，能破坏疱疹病毒的核糖核苷酸还原酶四级结构，从而抑制病毒复制。
T15378	Gemcitabine elaidate Gemcitabine 5'-elaidate,反油酸吉西他滨,吉西他滨反油酸酯,Gemcitabine (elaidate),CO-101,CP-4126	Apoptosis; Nucleoside Antimetabolite/Analog; Autophagy	Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Gemcitabine elaidate (CP-4126) 是 Gemcitabine 的亲脂性前药。它通过酯酶转化为 Gemcitabine 以被磷酸化。它具有抗肿瘤活性。
T37106	2'-Deoxyadenosine-5'-triphosphate (sodium salt hydrate)
	2'-Deoxyadenosine-5'-triphosphate (dATP) is a purine nucleotide and derivative of the nucleic acid adenosine 5'-triphosphate .1dATP is a substrate for DNA polymerase in the synthesis of DNA.2It is a noncompetitive inhibitor of ribonucleotide reductases, which provides feedback inhibition during DNA synthesis.1dATP has commonly been used in DNA synthesis, sequencing, and labeling in research applications.3,4dATP accumulates in adenosine deaminase deficiency, a disorder characterized by mutations ...
T63240	Lometrexol disodium
	Lometrexol (DDATHF) disodium 是人丝氨酸羟甲基转移酶 1/2 (hSHMT1/2) 的有效抑制剂，也是抗嘌呤类抗叶酸 (antifolate) 药，能够降低甘氨酰胺核糖核苷酸甲酰基转移酶 (GARFT) 的活性，但不引起可检测水平的 DNA 链断裂。Lometrexol disodium 对嘌呤从头合成具有抑制作用，可造成异常的细胞增殖，凋亡 (apoptosis) 和细胞周期停滞，表现出抗癌效果。
T74088	Fludarabine triphosphate trisodium
	Fludarabine triphosphate (F-ara-ATP) trisodium 是Fludarabine 的活性代谢物，是一种有效的、非竞争性的、特异性的DNA 引发酶 (DNA primase) 抑制剂，其IC50为 2.3 μM，Ki 为 6.1 μM。Fludarabine triphosphate trisodium 通过阻断 DNA 引发酶和引物 RNA 形成抑制 DNA 合成 (DNA synthesis)。Fludarabine triphosphate trisodium 可抑制核糖核苷酸还原酶和DNA 聚合酶，导致细胞凋亡 (apoptosis)。
T41297	Lometrexol hydrate
	Lometrexol hydrate (DDATHF hydrate) 是一种抗嘌呤类抗叶酸 (antifolate) 药，可抑制甘氨酰胺核糖核苷酸甲酰基转移酶 (GARFT) 的活性，但不会诱导可检测水平的 DNA 链断裂。Lometrexol hydrate 可以进一步抑制嘌呤从头合成，引起异常的细胞增殖和凋亡，甚至细胞周期停滞。Lometrexol hydrate 具有抗癌活性。Lometrexol hydrate 还是一种有效的人丝氨酸羟甲基转移酶 1/2 (hSHMT1/2) 抑制剂。
T60401	Tezacitabine
	Tezacitabine 是一种抑制细胞生长和细胞毒性的抗代谢物。 Tezacitabine 是一种核苷类似物，具有双重作用机制。 Tezacitabine 不可逆地抑制核糖核苷酸还原酶，并可在复制或修复过程中掺入 DNA，导致 DNA 链终止。 Tezacitabine 在细胞周期的 G1 期和 S 期阻断肿瘤细胞并诱导凋亡细胞死亡。 Tezacitabine 具有治疗白血病和实体瘤的潜力[1][2]。

化合物

AICAR monophosphate

Cat.No: T21195

Synonym: Aica ribonucleotide,AICA riboside,Acadesine 5'-monophosphate,Z-nucleotide

Target: Others

Cat.No: T9210

Target: CD73

Cat.No: T0297

Synonym: Clofarex,氯法拉滨,克罗拉滨,Evoltra,Clolar

Target: Apoptosis, Nucleoside Antimetabolite/Analog, DNA/RNA Synthesis, Autophagy

Cat.No: T14864

Synonym: NSC-253272,卡醋胺

Target: Others, DNA/RNA Synthesis, Antibacterial

Cat.No: T3157

Synonym: RNR Inhibitor COH29

Target: DNA/RNA Synthesis

Polydeoxyribonucleotide(Sodium salt)

Cat.No: T8855

Synonym: Polydeoxyribonucleotide from salmon

Target: Others

Cat.No: T0353

Synonym: Oxaphenamide,4'-Hydroxysalicylanilide,羟苯水杨胺,柳胺酚

Target: HBV, DNA/RNA Synthesis

Cat.No: T8800

Synonym: 2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide

Target: DNA/RNA Synthesis

Cat.No: T7525

Synonym: 3,4-二羟基苯甲羟肟酸,NSC-324360

Target: DNA/RNA Synthesis

Cat.No: T1982

Synonym: NSC663249,Triapine,PAN-811,OCX191

Target: DNA/RNA Synthesis

Cytidine 5'-diphosphate disodium

Cat.No: T31163

Synonym: CDP sodium salt,Cytidine 5'-diphosphate disodium salt,胞苷-5'-二磷酸二钠盐,Cytidine diphosphate sodium salt

Target: Others

Cat.No: T15826

Synonym: LY 264618,DDATHF

Target: DHFR

Fludarabine Phosphate

Cat.No: T6501

Synonym: NSC 312887 Phosphate,fludara Phosphate,F-ara-A (NSC 312887) Phosphate,F-ara-AMP,磷酸氟达拉滨

Target: Apoptosis, Nucleoside Antimetabolite/Analog, DNA/RNA Synthesis

Cat.No: T14147

Synonym: AG 2037

Target: DHFR

Cat.No: T68230

Cat.No: T11921

Target: DHFR

Cat.No: T29197

Cat.No: T24980

Synonym: 543U76,5-Deazacyclotetrahydrofolate

Cat.No: T26572

Synonym: AG-2034,AG 2034

Cat.No: T15813

Target: LTR

2’-Azido-2’-deoxycytidine

Cat.No: TNU0230

2'-Azido-2'-deoxyuridine

Cat.No: T10068

Synonym: N3dUrd

Target: Others

Cat.No: T11884

Target: Others

Cat.No: T82950

Fludarabine triphosphate

Cat.No: T40862

Synonym: 三磷酸氟达拉滨,F-ara-ATP

3’-Azido-3’-deoxycytidine

Cat.No: TNU0133

Cat.No: T78814

Target: DNA/RNA Synthesis

Uridine-5’-monophosphate (sodium salt hydrate)

Cat.No: T36300

Herpes virus inhibitor 2

Cat.No: T76517

Herpes virus inhibitor 1

Cat.No: T76515

Gemcitabine elaidate

Cat.No: T15378

Synonym: Gemcitabine 5'-elaidate,反油酸吉西他滨,吉西他滨反油酸酯,Gemcitabine (elaidate),CO-101,CP-4126

Target: Apoptosis, Nucleoside Antimetabolite/Analog, Autophagy

2'-Deoxyadenosine-5'-triphosphate (sodium salt hydrate)

Cat.No: T37106

Lometrexol disodium

Cat.No: T63240

Fludarabine triphosphate trisodium

Cat.No: T74088

Lometrexol hydrate

Cat.No: T41297

Cat.No: T60401

Cat. No.	Product Name	Target	Signaling Pathways
T5073	Inosine 5'-monophosphate disodium salt hydrate Inosine 5'-monophosphate disodium salt,5'-IMP-Na2,肌苷5-单磷酸二钠盐水合物,Disodium 5'-inosinate monohydrate	Others; Endogenous Metabolite	Metabolism; Others
	Inosine 5'-monophosphate disodium salt hydrate (Inosine 5'-monophosphate disodium salt) 或肌苷酸是次黄嘌呤的核糖核苷酸，是嘌呤合成过程中形成的第一个核苷酸。
T1705	5-Amino-3H-imidazole-4-Carboxamide 4-Amino-5-imidazolecarboxamide,AICA,4-氨基-5-咪唑甲酰胺,5-Aminoimidazole-4-carboxamide	Endogenous Metabolite	Metabolism
	5-Amino-3H-imidazole-4-Carboxamide (AICA) 是一种合成嘌呤（尤其是核碱基腺嘌呤和鸟嘌呤）的重要前体。
T4685	INOSINIC ACID Inosine 5′-monophosphate,IMP,5'-肌苷酸,I-5'-P	Endogenous Metabolite	Metabolism
	Inosinic acid (IMP) 是内源性代谢产物。
T4809	Pyrimidine 嘧啶,Metadiazine	Others; Endogenous Metabolite	Metabolism; Others
	Pyrimidine (Metadiazine) 是内源性代谢产物的一种。
T4826	L-Histidine monohydrochloride monohydrat	Others; Endogenous Metabolite	Metabolism; Others
	L-Histidine monohydrochloride monohydrat 是一种 α-氨基酸。 L-异构体是 22 种蛋白质氨基酸之一，即蛋白质的组成部分。

天然产物

Inosine 5'-monophosphate disodium salt hydrate

Cat.No: T5073

Synonym: Inosine 5'-monophosphate disodium salt,5'-IMP-Na2,肌苷5-单磷酸二钠盐水合物,Disodium 5'-inosinate monohydrate

Target: Others, Endogenous Metabolite

5-Amino-3H-imidazole-4-Carboxamide

Cat.No: T1705

Synonym: 4-Amino-5-imidazolecarboxamide,AICA,4-氨基-5-咪唑甲酰胺,5-Aminoimidazole-4-carboxamide

Target: Endogenous Metabolite

Cat.No: T4685

Synonym: Inosine 5′-monophosphate,IMP,5'-肌苷酸,I-5'-P

Target: Endogenous Metabolite

Cat.No: T4809

Synonym: 嘧啶,Metadiazine

Target: Others, Endogenous Metabolite

L-Histidine monohydrochloride monohydrat

Cat.No: T4826

Target: Others, Endogenous Metabolite

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