DNA Damage/DNA Repair(DNA损伤/DNA修复)
- MTH1(4)
- PARP(120)
- ATM/ATR(29)
- DNA Alkylating(23)
- DNA Ligases(3)
- DNA Methyltransferase(32)
- DNA-PK(31)
- HDAC(176)
- Nucleoside Antimetabolite/Analogue(158)
- Telomerase(15)
- Topoisomerase(182)
- tankyrase(5)
- Antifolate(33)
- CDK(269)
- Checkpoint Kinase (Chk)(32)
- CRISPR/Cas9(9)
- Deubiquitinase(76)
- DNA Alkylator/Crosslinker(73)
- DNA/RNA Synthesis(466)
- Eukaryotic Initiation Factor (eIF)(26)
- IRE1(23)
- LIM Kinase (LIMK)(12)
- TOPK(6)
- Casein Kinase(47)
- DNA Intercalating Agents(8)
- DNA/RNA Oxidative Damage(13)
- Poly(ADP-ribose) Glycohydrolase (PARG)(1)
- Early 2 Factor (E2F)(1)
- Cat.No. 产品名称 Information
-
GC15033
Azathioprine
硫唑嘌呤; BW 57-322
An immunosuppressive purine analog -
GC14106
Adenosine
腺苷; Adenine riboside; D-Adenosine
A purine nucleoside -
GC12423
Mycophenolate mofetil hydrochloride
RS 61443 hydrochloride; TM-MMF hydrochloride
A prodrug form of mycophenolic acid -
GC13729
Cytidine
胞苷; Cytosine β-D-riboside; Cytosine-1-β-D-ribofuranoside
A pyrimidine nucleoside -
GC13432
Adenine
腺嘌呤; 6-Aminopurine; Vitamin B4
腺嘌呤(6-氨基嘌呤)是一种嘌呤,是DNA核酸中的四种核碱基之一。腺嘌呤是DNA和RNA的化学成分。腺嘌呤还在涉及细胞呼吸、ATP 和辅因子(NAD 和 FAD)的形式以及蛋白质合成的生物化学中发挥重要作用。 -
GC11099
Doxifluridine
去氧氟尿苷; Ro 21-9738; 5-Fluoro-5'-deoxyuridine; 5'-DFUR
An antitumor prodrug of 5-fluorouracil -
GC13401
SJB3-019A
SJB3-019A 是一种有效的新型 USP1 抑制剂,在促进 K562 细胞中 ID1 降解和细胞毒性方面的作用是 SJB2-043 的 5 倍,IC50 为 0.0781 μM。
-
GC15663
LY2606368
5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368
LY2606368 是一种 ATP 竞争性 CHK1 抑制剂,目前处于临床阶段,Ki 为 0.9 nM,IC50 <1 nM。 -
GC17635
ML-323
A selective USP1-UAF1 deubiquitinase complex inhibitor
-
GC17848
Penciclovir
喷昔洛韦; BRL 39123; VSA 671
An antiviral guanosine analog -
GC10637
Zidovudine
叠氮胸苷; Azidothymidine; AZT; ZDV
A nucleoside reverse transcriptase inhibitor -
GC13831
FT-207 (NSC 148958)
替加氟; FT 207; NSC 148958
A prodrug form of 5-fluorouracil -
GC13667
Temozolomide
替莫唑胺; NSC 362856; CCRG 81045; TMZ
替莫唑胺是一种口服活性烷化剂,可诱导 DNA 中 O6-甲基鸟嘌呤的形成,其在随后的 DNA 复制周期中与胸腺嘧啶错配,从而激活细胞凋亡途径,替莫唑胺可穿过血脑屏障并适用于恶性神经胶质瘤和转移性黑色素瘤。 -
GC11048
Irinotecan HCl Trihydrate
盐酸伊立替康三水合物; (+)-Irinotecan hydrochloride trihydrate; CPT-11 hydrochloride trihydrate
A potent inhibitor of DNA topoisomerase I -
GC15377
LEE011 succinate
瑞博西尼琥珀酸盐; LEE011 succinate
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC15922
LEE011 hydrochloride
瑞博西尼盐酸盐; LEE011 hydrochloride
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC17466
LH846
A selective inhibitor of CK1δ
-
GC13328
XL413 hydrochloride
BMS-863233 hydrochloride
A potent inhibitor of Cdc7 -
GC18117
XL413
A potent inhibitor of Cdc7
-
GC12350
T 705
法匹拉韦; T-705
An antiviral agent -
GC11648
BML-277
Chk2 Inhibitor II
A selective DNA damage control kinase inhibitor -
GC13359
Topotecan HCl
盐酸拓扑替康; SKF 104864A Hydrochloride; NSC 609669 Hydrochloride
A potent inhibitor of DNA topoisomerase I -
GC17522
LY2334737
2'-脱氧-2',2'-二氟-N-(1-氧代-2-丙基戊基)胞苷
LY2334737 是一种核苷类似物,是吉西他滨的口服活性前药。 -
GC17865
Lomustine
洛莫司汀; CCNU; NSC 79037
A DNA alkylating agent -
GC14961
Cytarabine hydrochloride
盐酸阿糖胞苷; Cytosine β-D-arabinofuranoside hydrochloride; Cytosine Arabinoside hydrochloride; Ara-C hydrochloride
A nucleoside analog and prodrug form of ara-CTP -
GC11747
Amsacrine hydrochloride
盐酸胺苯吖啶,m-AMSA hydrochloride; acridinyl anisidide hydrochloride
A topoisomerase II poison -
GC12326
Amsacrine
安吖啶; m-AMSA; acridinyl anisidide
A topoisomerase II poison -
GC12828
Daunorubicin
柔红霉素; Daunomycin; RP 13057; Rubidomycin
Daunorubicin (Daunomycin) 是一种拓扑异构酶 II 抑制剂,具有有效的抗肿瘤活性。
-
GC10354
Daunorubicin HCl
盐酸柔红霉素; Daunomycin hydrochloride; RP 13057 hydrochloride; Rubidomycin hydrochloride
Antitumor antibiotic used in the treatment of acute myeloid leukemias -
GC13858
Torin 2
9-(6-氨基-3-吡啶基)-1-[3-(三氟甲基)苯基]苯并[H]-1,6-萘啶-2(1H)-酮
Selective inhibitor of mTOR -
GC11537
MK-4827 tosylate
尼拉帕尼对苯甲磺酸盐; MK-4827 tosylate
An orally bioavailable PARP1/2 inhibitor -
GC12756
MK-4827 hydrochloride
MK-4827 hydrochloride
MK-4827 hydrochloride (MK-4827 hydrochloride) 是一种高效且具有口服生物利用度的 PARP1 和 PARP2 抑制剂,IC50 分别为 3.8 和 2.1 nM。 MK-4827 hydrochloride 抑制 DNA 损伤的修复,激活细胞凋亡并显示出抗肿瘤活性。 -
GC11424
Valproic acid
丙戊酸; VPA; 2-Propylpentanoic Acid
A class I HDAC inhibitor -
GC17651
Sunitinib
舒尼替尼; SU 11248
舒尼替尼Sunitinib(SU 11248)是一种具口服活性的多靶点受体酪氨酸激酶抑制剂,对血管内皮生长因子受体(VEGFR2)和血小板衍生生长因子受体(PDGFRβ)的IC50分别为80nM和2nM。 -
GC14234
PF-477736
PF 00477736
A selective inhibitor of checkpoint kinase 1 -
GC16143
Varenicline Hydrochloride
6,7,8,9-四氢-6,10-甲桥-6H-吡嗪并[2,3-H][3]苯并氮杂卓盐酸盐,CP 526555 hydrochloride
Varenicline Hydrochloride (CP 526555 hydrochloride) 是一种高亲和力、选择性的 α4β2 尼古丁乙酰胆碱受体 (nAChR) 部分激动剂和完整的 α7 nAChR 激动剂。 -
GC15306
Calcium N5-methyltetrahydrofolate
N5-甲基四氢叶酸钙; NSC173328
N5-甲基四氢叶酸钙 (NSC173328) 是左旋叶酸的钙盐,已被提议用于治疗心血管疾病和晚期癌症,如乳腺癌和结肠直肠癌。 -
GC17139
APY29
A modulator of IRE1α function
-
GC14974
AMG 925
A dual inhibitor of FLT3 and Cdk4
-
GC10734
Beta-Lapachone
3,4-二氢-2,2-二甲基-2H-萘并[1,2-B]吡喃-5,6-二酮,ARQ-501; NSC-26326
An anti-cancer quinone -
GC14364
SGI-1027
DNA Methyltransferase Inhibitor II
A DNA methyltransferase inhibitor -
GC13013
TCID
4,5,6,7-四氯茚满-1,3-二酮,4,5,6,7-Tetrachloroindan-1,3-dione
A potent, selective inhibitor of UCH-L3 -
GC12011
P276-00
P276-00
P276-00 (P276-00) 是一种有效的细胞周期蛋白依赖性激酶 (CDK) 抑制剂,可抑制 CDK9-cyclinT1、CDK4-cyclin D1 和 CDK1-cyclinB,IC50 分别为 20 nM、63 nM 和 79 nM。 P276-00 (P276-00) 对顺铂耐药细胞具有抗肿瘤活性。 -
GC15337
VE-822
ATR抑制剂
-
GC17897
Triapine
[(3-氨基吡啶-2-基)亚甲基氨基]硫脲
核糖核苷酸还原酶抑制剂 -
GC17231
CRT0044876
7-硝基吲哚-2-甲酸
A cell-permeable inhibitor of Ape-1 -
GC13419
ME0328
A selective PARP3 inhibitor
-
GC17703
TMP269
TMP 269;TMP-269
A selective class IIa HDAC inhibitor -
GC14285
RGFP966
RGFP 966;RGFP-966
RGFP966是一种N-(o-aminophenyl)carboxamide HDAC抑制剂,对HDAC3的IC50为0.08 μM,是一类针对HDAC3的慢开/慢关竞争性紧密结合抑制剂。 -
GC13136
(S)-Crizotinib
An MTH1 inhibitor