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16
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10165L |
5-A-RU hydrochloride
5-Amino-6-(D-ribitylamino)uracil hydrochloride |
Others | Others |
5-A-RU hydrochloride (5-Amino-6-(D-ribitylamino)uracil hydrochloride) 是细菌核黄素的中间体,可激活粘膜相关不变 T 细胞(MAIT)。5-A-RU 可用于研究乳腺癌和前列腺癌。 | |||
T35439 |
(E)-5-(2-Bromovinyl)uracil
|
||
(E)-5-(2-Bromovinyl)uracil (BVU) is a pyrimidine base and an inactive metabolite of the antiviral agents sorivudine and (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) that may be regenerated to BVDU in vivo. BVU irreversibly inactivates dihydropyrimidine dehydrogenase (DPD) in an NADPH-dependent manner. It enhances the efficacy of the chemotherapeutic agent and DPD substrate 5-fluorouracil in a P388 murine leukemia model when administered at a dose of 200 μmol/kg, increasing survival time. | |||
T60333 | Cyclopentenyl uracil | ||
Cyclopentenyl uracil 是一种无细胞毒性的尿苷激酶 (uridine kinase) 抑制剂,可有效阻断完整小鼠体内宿主和肿瘤组织对循环尿苷的回收。 | |||
T60780 |
Tegafur-Uracil
|
||
Tegafur-Uracil 是可用于抗实体肿瘤相关研究的,具有口服活性的氟尿嘧啶类抗癌剂,可抑制胸苷酸合成酶。 | |||
T10165 |
5-A-RU
5-Amino-6-(D-ribitylamino)uracil |
Others | Others |
5-A-RU (5-Amino-6-(D-ribitylamino)uracil), a precursor of bacterial Riboflavin, is a mucosal-associated invariant T (MAIT) cells activator. 5-A-RU forms potent MAIT-activating antigens via non-enzymatic reactions with small molecules that are derived from | |||
TNU0014 |
1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil
|
Apoptosis | Apoptosis |
1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil is a Nucleoside, fluoro-modified nucleoside; Arabino-nucleosidde. | |||
TNU1543 |
(S)-DMT-glycidol-uracil
|
||
(S)-DMT-glycidol-uracil is a Nucleoside Derivative - Acyclic nucleoside. | |||
T74868 | Uracil-m7GpppAmpG ammonium | ||
Uracil-m7GpppAmpG ammonium 是一种帽类似物,可用于 mRNA 的合成。 | |||
TNU0870 |
5-(2-Hydroxyethyl)uracil
|
||
5-(2-Hydroxyethyl)uracil bolongs toIntermediates and Building Blocks - Nucleoside base, Nucleophile; Heterocylic Compounds - Pyrimidine; Scaffold and Template. | |||
TNU0872 |
5-(3-Hydroxypropyl)uracil
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5-(3-Hydroxypropyl)uracil bolongs toIntermediates and Building Blocks - Nucleoside base, Nucleophile; Heterocylic Compounds - Pyrimidine; Scaffold and Template. | |||
TNU0264 |
1-(b-D-Xylofuranosyl)uracil
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1-(b-D-Xylofuranosyl)uracil is a Nucleoside Derivative - Xylo-nucleoside. | |||
TNU1446 |
7'-O-DMT-morpholino uracil
|
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7'-O-DMT-morpholino uracil is a Nucleoside Derivative - Morpholino nucleoside. | |||
T20092 |
Lenacil
634 Hexilure,环草定,Herbicide |
Others | Others |
Lenacil (634 Hexilure) 是选择性尿嘧啶取代的除草剂,用于控制甘蔗,豌豆,苜蓿,苹果,桃子,薄荷和甜菜中的一年生草,阔叶杂草和一些多年生杂草,能够抑制光合作用。 | |||
TNU1586 |
7’-OH-N-DMTr morpholino uracil
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7'-OH-N-DMTr morpholino uracil is a Nucleoside Derivative - Morpholino nucleoside. | |||
TNU1453 |
5-Bromo-N1-t-butoxycarbonylmethyl-uracil
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||
5-Bromo-N1-t-butoxycarbonylmethyl-uracil is a PNA-related Derivative. | |||
T75189 | 5-Caroxy uracil-1-yl acetic acid benzyl ester | ||
5-Caroxy uracil-1-yl acetic acid benzyl ester 是一种嘌呤核苷类似物,其抗肿瘤活性广泛,主要针对惰性淋巴系统恶性肿瘤。该化合物通过抑制 DNA 合成、诱导细胞凋亡(apoptosis)等机制发挥抗癌作用。 | |||
TNU1460 | Tr-morpholino-U; 7’-OH-N-trityl morpholino uracil | ||
Nucleoside Derivatives –Morpholino nucleosides | |||
TNU1012 |
1-[6-Phosphono-2-O-methyl-β-D-ribo-hexofuranosyl]uracil
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1-[6-Phosphono-2-O-methyl-β-D-ribo-hexofuranosyl]uracil is a Nucleoside Derivative - Phosphorus-containing nucleotide; 2'-Modified nucleoside; 5'-Modified nucleoside; 2'-Modified nucleoside. | |||
TNU0928 |
1-(5-O-Methoxytrityl-2-deoxy-b-D-xylofuranosyl)uracil
|
||
Nucleoside Derivatives - Xylo-nucleosides, 2’-Deoxy-nucleosides; ; Protected nucleosides with NH2/OH group | |||
TNU1011 |
1-[6-(Diethoxyphosphinyl)-2-O-methyl-β-D-ribo-hexofuranosyl]uracil
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1-[6-(Diethoxyphosphinyl)-2-O-methyl-β-D-ribo-hexofuranosyl]uracil is a Nucleoside Derivative - Phosphorus-containing nucleotide; 2'-Modified nucleoside; 5'-Modified nucleoside; 2'-Modified nucleoside. | |||
TNU1286 | 1-[6-(Diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hexofuranosyl]uracil | ||
Nucleoside Derivatives - Phosphorus-containing nucleosides; 2’-Modified nucleosides; 5’-Modified nucleosides | |||
TNU1010 |
1-[(5E)-5,6-Dideoxy-6-phosphono-2-O-methyl-β-D-ribo-hex-5-enofuranosyl)uracil
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1-[(5E)-5,6-Dideoxy-6-phosphono-2-O-methyl-β-D-ribo-hex-5-enofuranosyl)uracil is a Nucleoside Derivative - Phosphorus-containing nucleotide; 2'-Modified nucleoside; 5'-Modified nucleoside; 2'-Modified nucleoside. | |||
TNU1008 | 1-[(5E)-5,6-Dideoxy-6-(diethoxyphosphinyl)-2-O-methyl-β-D-ribo-hex-5-enofuranosyl]uracil | ||
Nucleoside Derivatives - Phosphorus-containing nucleotide; 2’-Modified nucleoside; 5’-Modified nucleoside | |||
TNU1285 | 1-[(5E)-5,6-Dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil | ||
1-[(5E)-5,6-Dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 TNU1285。 | |||
TNU1288 |
1-[(5E)-3-O-[(Bis-diisopropyl amino)(2-cyano ethoxy)phosphino]-5,6-dideoxy-6-(diethoxy phosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil
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1-[(5E)-3-O-[(Bis-diisopropyl amino)(2-cyano ethoxy)phosphino]-5,6-dideoxy-6-(diethoxy phosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil is a Nucleoside Phosphoramidite; Nucleoside Derivative - Phosphorus-containing nucleotide; 5'-Modified nucleoside. | |||
TNU0087 |
4’-Azido-2’-deoxy-2’-fluoro-beta-D-arabinouridine
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Fluoro-modified nucleoside; Azido-nucleoside; Arabino-nucleoside | |||
TNU1608 |
DMTr-TNA-U-amidite
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DMTr-TNA-U-amidite is a Nucleoside Phosphoramidite. | |||
TNU1009 |
VP-U-6
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VP-U-6 is a Nucleoside Phosphoramidite; Nucleoside Derivative - Phosphorus-containing nucleotide; 5'-Modified nucleoside. | |||
T0984 |
5-Fluorouracil
5-FU,Fluorouracil,5-氟脲嘧啶,NSC 19893,5-Fluoracil,氟尿嘧啶 |
Apoptosis; Nucleoside Antimetabolite/Analog; HIV Protease; DNA/RNA Synthesis; Endogenous Metabolite | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Proteases/Proteasome |
5-Fluorouracil (5-FU) 是一种尿嘧啶类似物,一种 DNA 合成抑制剂。5-Fluorouracil 具有抗肿瘤活性,通过抑制胸苷酸合成酶影响嘧啶的合成。5-Fluorouracil 可以引起细胞凋亡和自噬。 | |||
T9463 |
6-HYDROXYLAMINOURACIL
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Others | Others |
6-HYDROXYLAMINOURACIL 是尿嘧啶的衍生物,它可以诱导肿瘤细胞的 DNA 损伤和凋亡,在体外抑制肿瘤细胞的生长。 | |||
T8613 |
1-Ethyl-6-aminouracil
6-AMINO-1-ETHYL-1H-PYRIMIDINE-2,4-DIONE,1-乙基-6-氨基脲嘧啶 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
1-Ethyl-6-aminouracil (6-AMINO-1-ETHYL-1H-PYRIMIDINE-2,4-DIONE) 是合成一系列新的取代黄嘌呤的中间体,这些黄嘌呤对人腺苷 A2B 受体具有高亲和力和选择性。 | |||
T1309 |
Propylthiouracil
丙硫氧嘧啶,Pseudocapsaicin,NSC 6498,丙基硫氧嘧啶,NSC 70461,6-n-Propylthiouracil,6-Propyl-2-thiouracil |
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Propylthiouracil (6-n-Propylthiouracil) 是一种甲状腺过氧化物酶抑制剂,也是一种5'-脱碘酶抑制剂。 | |||
T7614 |
Eniluracil
GW776C85,5-Ethynyluracil |
Others | Others |
Eniluracil (GW776C85) 是不可逆的二氢嘧啶脱氢酶(DPD)抑制剂,是一种尿嘧啶类似物,能够使 5-FU 的口服生物利用度提高到 100%,促进均匀吸收和可预测的毒性。 | |||
TNU0187 |
2',5-Difluoro-2'-deoxy-1-arabinosyluracil
2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2',5-Difluoro-2'-deoxy-1-arabinosyluracil (2'-Deoxy-2'-fluoro-5-fluoro-arabinouridine) 是一种尿嘧啶核苷类似物,具有潜在的抗癫痫活性和降压活性,可用于研究抗惊厥和焦虑症。 | |||
T0304 |
Methylthiouracil
甲基硫脲嘧啶,甲硫氧嘧啶,NSC-193526,NSC-9378,MTU |
ERK; Antiviral; TNF; NF-κB; Interleukin | Apoptosis; Immunology/Inflammation; MAPK; NF-κB |
Methylthiouracil (NSC-193526) 是一种抗甲状腺剂。它抑制TNF-α和IL-6的产生以及NF-κB 和ERK1/2的活化。 | |||
T24173 |
Iodothiouracil
Iothiouracil,Jodthiouracilum |
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Iodothiouracil is a uracil derivative. It was used as a thyroid antagonist. | |||
T36235 |
5-Chlorouracil
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5-Chlorouracil is a chlorinated derivative of the pyrimidine nucleoside base uracil . In vivo, it is converted into chlorodeoxyuridine, which is mutagenic and genotoxic.1 Uracil is chlorinated at the 5 position in a cell-free myeloperoxidase, peroxide, and chloride system in which hypochlorous acid is formed.2 5-Chlorouracil has been found in human neutrophils stimulated with phorbol 12-myristate 13-acetate in vitro and in inflammatory human exudate isolated from sites of superficial infection. ... | |||
TNU0814 | 5-Azauracil | ||
Heterocyclic Compounds –Triazine; Intermediates and Building Blocks - Nucleophile; Nucleoside base | |||
TNU0700 | 5-Hydroxymethyl-2-thiouracil | ||
Heterocyclic compound - pyrimidine; building block - nucleobase | |||
T36895 |
5-Fluorouracil-13C,15N2
5-Fluorouracil-13C,15N2 |
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5-Fluorouracil-13C,15N2 is intended for use as an internal standard for the quantification of 5-flurouracil by GC- or LC-MS. 5-Fluorouracil is a pyrimidine analog that irreversibly inhibits thymidylate synthase, blocking the synthesis of thymidine which is required for DNA synthesis. Intracellular metabolites of 5-fluorouracil exert cytotoxic effects by either inhibiting thymidylate synthetase, or through incorporation into RNA and DNA, ultimately initiating apoptosis. | |||
TNU0371 |
1-(b-D-Xylofuranosyl)-2-thiouracil
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Nucleoside Derivatives - Xylo-nucleosides, Thio-nucleosides | |||
TNU1060 |
6-Mthyluracil-1-yl acetic acid methyl ester
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6-Mthyluracil-1-yl acetic acid methyl ester is a PNA-related Derivative. | |||
TNU0628 |
5-Iodouracil
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5-Iodouracil is a Heterocyclic compound-pyrimidine, intermediate and building block, halo-. | |||
TNU1052 |
5-Fluorouracil-1-yl acetic acid methyl ester
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5-Fluorouracil-1-yl acetic acid methyl ester is a PNA-related Derivative. | |||
TNU1289 |
1-[(5E)-3-O-[(Bis-di-isopropyl amino)(2-cyanoethoxy) phosphino]-5,6-dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]-5-methyluracil
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1-[(5E)-3-O-[(Bis-di-isopropyl amino)(2-cyanoethoxy) phosphino]-5,6-dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]-5-methyluracil is a Nucleoside Phosphoramidite; Nucleoside Derivative - Phosphorus-containing nucleotide; 5'-Modified nucleoside. | |||
TNU1054 |
5-Trifluoromethyluracil-1-yl acetic acid methyl ester
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5-Trifluoromethyluracil-1-yl acetic acid methyl ester is a PNA-related Derivative. | |||
TNU1053 |
5-Fluorouracil-1-yl acetic acid
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5-Fluorouracil-1-yl acetic acid is a PNA-related Derivative. | |||
TNU1058 |
5-Methoxyuracil-1-yl acetic acid
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5-Methoxyuracil-1-yl acetic acid is a PNA-related Derivative. | |||
T29611 | Acluracil | ||
Acluracil is a biochemical. | |||
T36870 |
5,6-dihydro-5-Fluorouracil
5-fluorodihydrouracil,5-Fluoro-dihydro-pyrimidine-2,4-dione |
Others | Others |
5,6-dihydro-5-Fluorouracil (5-FUH2)是 5-FU 的无活性代谢产物,可用于用于研究机体代谢。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0069 |
Uracil
|
Others; Endogenous Metabolite | Metabolism; Others |
Uracil 是普遍存在的天然嘧啶衍生物,是 RNA 核酸中的四个碱基之一。 | |||
T5255 |
5-Hydroxymethyluracil
5-(Hydroxymethyl)uracil,5-羟甲基脲嘧啶,Hydroxymethyl Uracil,a-Hydroxythymine |
Others; Endogenous Metabolite | Metabolism; Others |
5-Hydroxymethyluracil (a-Hydroxythymine) 是一种氧化性 DNA 损伤的产物,能够增强或抑制细菌 RNA 聚合酶转录的潜在表观遗传标记。 | |||
T4711 |
2,4-Dihydroxypyrimidine-5-carboxylic acid
脲嘧啶-5-羧酸,Isoorotic acid,Uracil-5-carboxylic acid |
Others; Endogenous Metabolite | Metabolism; Others |
2,4-Dihydroxypyrimidine-5-carboxylic acid (Isoorotic acid) 是内源性代谢产物的一种。 | |||
T1721 |
2'-Deoxyuridine
Uracil deoxyriboside,2-deoxyuridine,2'-dU,2'-脱氧尿苷 |
Others; DNA/RNA Synthesis; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Others |
2'-Deoxyuridine (2-deoxyuridine) 可以促使染色体断裂,从而抑制 thymidylate 的合成活性,它也是合成 Edoxudine 的前体。 | |||
T5979 |
1-beta-D-Arabinofuranosyluracil
阿糖尿苷,1-β-D-阿糖尿苷,Uracil 1-β-D-arabinofuranoside |
Others | Others |
1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) 是一种甲氧基腺苷衍生物,从加勒比海绵 Tectitethya crypta 中分离得到。已经证明其具有多种生物活性,如抗炎活性,缓解疼痛和血管舒张特性。它能够抑制小鼠淋巴瘤细胞的增殖。 | |||
T4886 |
Dihydrouracil
二氢尿嘧啶,5,6-Dihydrouracil |
Endogenous Metabolite | Metabolism |
Dihydrouracil (5,6-Dihydrouracil) 是一种尿嘧啶的代谢产物,能够作为鉴定二氢嘧啶脱氢酶 (DPD) 缺陷的标志物。 | |||
T1310 |
2-Thiouracil
Thiouracil,硫代由雪,Deracil,2-硫脲嘧啶 |
Thyroid hormone receptor(THR); NO Synthase | Endocrinology/Hormones; Immunology/Inflammation |
2-Thiouracil (Deracil) 是神经型一氧化氮合酶 (nNOS) 的选择性抑制剂(Ki:20 μM),是一种抗甲状腺化合物,可用作高度特异性的黑色素瘤探测物。 | |||
T0532 |
5,6-Dihydro-5-methyluracil
5, 6-Dihydrothymine,二氢朐腺嘧啶,Dihydrothymine |
Nucleoside Antimetabolite/Analog; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
5,6-Dihydro-5-methyluracil (Dihydrothymine) 是胸腺嘧啶的中间代谢产物之一,来源于动植物,浓度过高时会产生毒性。 | |||
T8060 |
5-Bromouracil
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Others | Others |
5-Bromouracil 通过诱导 A 型样 DNA 破坏核小体定位。 | |||
T40717 |
6-Methyluracil
Pseudothymine,6-甲基尿嘧啶 |
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6-Methyluracil, also known as Pseudothymine, is a metabolite derived from Uracil. It serves as an indicator for the accumulation of acetoacetyl-CoA (AACoA). Additionally, 6-Methyluracil has been observed to possess antiradiation properties in vivo. | |||
T2221 |
Uridine
Uridin,β-Uridine,NSC 20256,尿苷 |
Others; Endogenous Metabolite | Metabolism; Others |
Uridine (Uridin) 是一种核苷化合物, 由核糖环和尿嘧啶组成, 两者通过β-N1-配糖键链接。 | |||
T4718 |
Uridine 5'-monophosphate
Uridylic acid,尿苷5-单磷酸,UMP,Uridine phosphate,Uridine 5'-phosphoric acid,5'-Uridylic acid |
Others; Endogenous Metabolite | Metabolism; Others |
Uridine 5'-monophosphate (Uridylic acid) 是一种单磷酸盐形式的尿嘧啶核苷酸,能够由从头途径或体内核苷酸和核酸的降解产物获得,是哺乳动物乳中的主要核苷酸类似物。 | |||
TWO2759 |
Thymine
胸腺嘧啶,5-methyluracil |
Others; Endogenous Metabolite | Metabolism; Others |
Thymine (5-methyluracil) 是 DNA 的四个碱基之一,在动物癌症模型中,能够作为5-氟尿嘧啶的靶标,其 Km=2.3 μM。 | |||
T4809 |
Pyrimidine
嘧啶,Metadiazine |
Others; Endogenous Metabolite | Metabolism; Others |
Pyrimidine (Metadiazine) 是内源性代谢产物的一种。 | |||
T4919 |
Ureidopropionic acid
Carbamoyl-b-alanine,3-酰脲丙酸,3-Ureidopropionic acid |
Endogenous Metabolite | Metabolism |
Ureidopropionic acid (3-Ureidopropionic acid) 是尿嘧啶代谢的中间体。更具体地说,它是二氢尿嘧啶的分解产物,由二氢嘧啶酶产生。它通过β -脲丙酸酶进一步分解为β -丙氨酸。尿素丙酸本质上是β -丙氨酸的尿素衍生物。高水平的尿丙酸存在于β -尿丙酸酶(UP)缺乏的个体中。嘧啶代谢中的酶缺乏与抗肿瘤药物5-氟尿嘧啶的严重毒性风险有关。 | |||
T35770 |
Cylindrospermopsin
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Cylindrospermopsin, a tricyclic uracil derivative, is a cyanobacterial toxin that was first discovered in an algal bloom contaminating a local drinking supply on Palm Island in Queensland, Australia after an outbreak of a mysterious disease. Cylindrospermopsin targets protein and glutathione synthesis in hepatocytes (IC50s = 1.3 and 2.4 µM, respectively), leading to cell death. [1] It has been shown to inhibit the activity of the uridine monophosphate synthase complex with a Ki value of 10 &... |