Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2627 |
Nolatrexed dihydrochloride
盐酸诺拉曲塞,Thymitaq,AG 337 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nolatrexed dihydrochloride (Thymitaq) 是一种非竞争性的胸苷酸合酶抑制剂,能够在癌细胞 S 期诱导细胞周期停滞,具有抗癌活性。它与该酶的叶酸辅因子结合位点相互作用,对人胸苷酸合酶的Ki 值为 11 nM。 | |||
T33762 |
Fosifloxuridine nafalbenamide
NUC-3373,NUC3373,NUC 3373 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Fosifloxuridine nafalbenamide (NUC 3373) 是一种胸腺嘧啶合酶抑制剂,属于嘧啶核苷酸类似物,具有抗癌活性。它能诱发宿主免疫反应,有潜力增强免疫治疗。 | |||
T3658 |
Trifluridine/tipiracil hydrochloride mixture
Trifluridine-tipiracil hydrochloride mixture,TAS102,TAS-102,TAS 102 |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Trifluridine/tipiracil hydrochloride mixture (TAS-102) 是一种新型口服组合药物,含有摩尔比为 2:1 的曲氟尿苷(TFT) 和盐酸替吡嘧啶 (TTP)。它主要通过抑制胸苷酸合酶 (TS) 和掺入 DNA 来显示抗肿瘤活性。 | |||
T6632 |
Raltitrexed
ZD1694,雷替曲塞,D1694,ICI-D1694,Tomudex |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Raltitrexed (D1694) 是一种抗代谢药物,通过抑制胸苷酸合成酶起作用,可用于化疗。 | |||
T1428 |
Trifluridine
曲氟尿苷,NSC 529182,Trifluorothymidine,5-Trifluorothymidine,NSC 75520,曲氟胸苷,Viroptic,Trifluridina |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Trifluridine (NSC-75520) 是一种氟化胸苷类似物,具有潜在的抗肿瘤活性,还具有抗病毒活性。它掺入 DNA 并抑制胸苷酸合酶,从而抑制 DNA 合成、抑制蛋白质合成和细胞凋亡。 | |||
T4228 |
Nolatrexed
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nolatrexed 是一种胸苷酸合成酶抑制剂,具有潜在的抗癌活性。 | |||
T27399 |
Galocitabine
RO 091390,RO-091390,RO091390,RO-09-1390,Neofrutulon |
Others | Others |
Galocitabine (Neofrutulon) 是一种胸苷酸合成酶抑制剂,可能用于治疗癌症。 | |||
T0189 |
Pemetrexed
Pemetrexed acid,培美曲塞,LY231514,培美曲唑,LY-231514 Disodium Hydrate |
DHFR; DNA/RNA Synthesis; Antifolate; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Pemetrexed (LY-231514 Disodium Hydrate) acid 是一种鸟嘌呤衍生的抗肿瘤药物,可结合并抑制胸苷酸合酶、二氢叶酸还原酶和甘氨酰胺核苷酸甲酰转移酶的 Ki 分别为 1.3 nM、7.2 nM 和 65 nM。 | |||
T0964 |
Floxuridine
氟尿苷,5-Fluorouracil 2'-deoxyriboside,FUDR,Deoxyfluorouridine,NSC 27640 |
Apoptosis; Nucleoside Antimetabolite/Analog; Others; DNA/RNA Synthesis; Antibacterial; HSV | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Floxuridine (FUDR) 是一种嘧啶类似物,也是一种抗肿瘤代谢物。它抑制胸苷酸合成酶,导致 DNA 合成中断和细胞毒性。它是一种可诱导细胞凋亡的金黄色葡萄球菌感染抑制剂 ,具有抗HSV 和CMV 病毒的作用。 | |||
T19833 |
5-Fluoroorotic acid
|
DNA/RNA Synthesis; Antifungal | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
5-Fluoroorotic 是一种胸苷酸合成酶的抑制剂,是酵母分子遗传学中的一种选择性试剂。它具有与 5-fluorocytosine 相近的良好表达的抗念珠菌作用,以及适度的抗皮肤真菌作用。 | |||
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。 | |||
T4382 |
Proguanil hydrochloride
Paludrine hydrochloride,盐酸氯胍,Chlorguanide hydrochloride,Chloroquanil |
Others; Dehydrogenase; DNA/RNA Synthesis; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Others |
Proguanil hydrochloride (Chloroquanil) 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 | |||
T21314 |
Amsilarotene
TAC-101,TAC 101,TAC101 |
CDK | Cell Cycle/Checkpoint |
Amsilarotene (TAC101) 是口服有活性的合成类视黄醇,对视黄酸受体 α (RAR-α) 具有选择性亲和力,对 RAR-α 和 RAR-β 的 Ki=为 2.4 nM 和 400 nM。它可造成人胃癌、卵巢癌细胞及肝细胞癌的凋亡,可用于研究癌症。 | |||
T1852 |
Rac-Belinostat
NSC726630,PXD101,PX-105684 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Rac-Belinostat (PX-105684) 是一种具有抗肿瘤活性的新型异羟肟酸型组蛋白脱乙酰酶 (HDAC) 抑制剂。 Belinostat 靶向 HDAC 酶,从而抑制肿瘤细胞增殖、诱导细胞凋亡、促进细胞分化和抑制血管生成。这种药物可以使耐药肿瘤细胞对其他抗肿瘤药物敏感,可能是通过一种涉及胸苷酸合酶下调的机制。 | |||
T30761 |
CB 3703
CB3703,NSC 289522,CB-3703 |
||
CB 3703 is an inhibitor of dihydrofolate reductase and thymidylate synthase. | |||
T24454 |
Metesind Glucuronate
AG 331,AG331,AG-331 |
||
Metesind Glucuronate is an antineoplastic. It also is a specific thymidylate synthase inhibitor. | |||
T24991 |
8-Deazahomofolic acid
|
||
8-Deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor. | |||
T28023 |
Metesind
AG331,AG-341,AG-331,AG341 |
||
Metesind, a thymidylate synthase inhibitor, is used potentially for the treatment of brain cancer and solid tumours. | |||
T30760 |
CB 30900
CB30900,CB-30900 |
||
CB30900 is a novel and effective thymidylate synthase inhibitor. | |||
T25519 |
ICI 198583
CB 3819,ICI198583,ICI-198583 |
||
ICI 198583 is an inhibitor of antifolate thymidylate synthase. | |||
T12674 |
(Rac)-Plevitrexed
(Rac)-ZD 9331,(Rac)-BGC9331 |
Others | Others |
(Rac)-Plevitrexed is a racemate of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS). | |||
T30763 |
CB 3731
CB3731,CB-3731 |
||
CB 3731 is used in fluorine-19 nuclear magnetic resonance studies of binary and ternary complexes of thymidylate synthase. | |||
T27349 |
Fosfluridine tidoxil
HDP 990006,HDP990006,HDP-990006 |
||
Fosfluridine tidoxil, a thymidylate synthase inhibitor, is used potentially for the treatment of colorectal cancer, and breast cancer. | |||
T71623 |
ICI-M247496
|
||
ICI-M247496 is a non-polyglutamated analog of CB3717 and quinazoline-based inhibitor of thymidylate synthase. | |||
T12635 |
(R)-Plevitrexed
(R)-ZD 9331,(R)-BGC9331,(R)-普来曲塞 |
Others | Others |
(R)-Plevitrexed is a less active enantiomer of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS). | |||
T21315 |
Folitixorin
ANX-510 |
||
ANX-510 is a folate-based biomodulator. It stabilizes the covalent binding of the fluorouracil metabolite FdUMP to thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituen | |||
T24981 |
5,6,7,8-Tetrahydro-8-deazahomofolic acid
5,6,7,8-Tdfa |
||
5,6,7,8-Tetrahydro-8-deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor. | |||
T24572 |
OSI-7904L free acid
OSI 7904,OSI-7904L,OSI7904,OSI 7904L,OSI7904L,OSI-7904 |
||
OSI-7904L is a folate-based thymidylate synthase inhibitor. It also has antimalarial and antitumor properties. | |||
T62996 | 10-Formyl-5,8-dideazafolic acid | ||
10-Formyl-5,8-dideazafolic acid 是一种胸苷酸合成酶 (thymidylate synthase) 抑制剂。 | |||
T69268 |
BGC-638
|
||
BGC-638, an analogue of BGC-945, is a thymidylate synthase inhibitor specifically transported into α-folate receptor (α-FR)–overexpressing tumors. | |||
T70583 |
Pemetrexed Diethyl Ester
|
||
Pemetrexed Diethyl Ester is a protected intermediate in the synthesis of Pemetrexed, a multi-targeted anti-folate that inhibits thymidylate synthase as well as other folate dependent enzymes. | |||
T12635L |
Plevitrexed
BGC9331,ZD 9331 |
Others | Others |
Plevitrexed is taken up via the α-folate receptor as well as the reduced folate carrier. Plevitrexed is an orally active and effective thymidylate synthase (TS) inhibitor (Ki: 0.44 nM). Plevitrexed is used for gastric cancer in clinical. | |||
T38490 |
ONX 0801 trisodium
Idetrexedtrisodium,BGC 945 trisodium,CB300945trisodium |
||
ONX 0801 (BGC 945) trisodium is a targeted thymidylate synthase (TS) inhibitor specifically designed to act against tumors overexpressing the α-folate receptor. | |||
T63401 | EGFR/HER2/TS-IN-1 | ||
EGFR/HER2/TS-IN-1 是 EGFR、HER2和TS (Thymidylate synthase)抑制剂,他们的IC50值分别为 0.203、0.088 和 0.168 μM,具有诱导 MCF7 细胞凋亡(apoptosis)的作用。 | |||
T66032 |
Pemetrexed disodium heptahydrate
|
||
Pemetrexed disodium is a guanine-derived antineoplastic agent that functions as a nucleic acid synthesis inhibitor through its binding to, and inhibition of, thymidylate synthase. | |||
T36895 |
5-Fluorouracil-13C,15N2
5-Fluorouracil-13C,15N2 |
||
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. | |||
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。 | |||
T78751 |
DG1
|
||
DG1(化合物8Nc)是一种Thymidylate Synthase(TS)抑制剂,具有抑制NSCLC细胞的血管生成和代谢重编程作用。此外,DG1还能有效下调CD26、ET-1、FGF-1和EGF的表达,并在A549异种移植小鼠模型中显著抑制肿瘤组织的增殖。 | |||
T77237 |
N,O-Didansyl-L-tyrosine cyclohexylammonium
|
||
N,O-Didansyl-L-tyrosine cyclohexylammonium 是一种有效的选择性胸苷酸合成酶 (TS) 抑制剂,作用于Escherichia coli,Lactobacillus casei 和人的 TS 的IC50值分别是 5.0,3.4 和 119 μM。 | |||
T36096 |
Thiocoraline
|
||
Thiocoraline is a depsipeptide and DNAbis-intercalator originally isolated fromMicromonosporawith antibacterial and anticancer activities.1,2It is active against the Gram-positive bacteriaS. aureus,B. subtilis, andM. luteus(MICs = 0.05, 0.05, and 0.03 μg/ml, respectively) but not Gram-negativeE. coli,K. pneumoniae, orP. aeruginosa(MICs = >100 μg/ml for all).1Thiocoraline inhibits RNA and DNA polymerase and thymidylate synthase (IC50s = 6, 6, and 15 μg/ml, respectively), as well as RNA and DNA sy... |