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
-
GC12869
JW 55
Tankyrase 1/2 Inhibitor IV
A TNKS1/2 inhibitor -
GC12991
EB 47
A PARP1 and TNKS2 inhibitor
-
GC12680
DR 2313
3,5,7,8-四氢-2-甲基-4H-硫代吡喃并[4,3-D]嘧啶-4-酮
A PARP inhibitor -
GC14434
BYK 49187
Potent PARP-1/PARP-2 inhibitor
-
GC10690
BYK 204165
PARP Inhibitor XIV
A selective inhibitor of PARP1 -
GC16474
4-HQN
4-羟基喹唑啉
A heterocyclic building block -
GC16386
Tubacin
HDAC6抑制剂
Tubacin (tubulin acetylation inducer)是一种选择性抑制组蛋白去乙酰化酶6 (HDAC6),诱导α-微管蛋白乙酰化的小分子,IC50为0.004µM。 -
GC13591
TC-H 106
RGFA-8; TC-H 106; Histone Deacetylase Inhibitor VII
A tight-binding inhibitor of class I HDACs -
GC11095
Pyroxamide
N-羟基-N'-3-吡啶基辛二酰胺
A HDAC inhibitor -
GC15040
NSC 3852
8-羟基-5-硝基喹啉
A tumor cell differentiating agent -
GC15536
NCH 51
NCH-51
An HDAC inhibitor -
GC13435
KD 5170
An inhibitor of class I and II HDACs
-
GC12393
Melphalan
Alanine Nitrogen Mustard, Alkeran, NSC 8806, NSC 241286, L-Phenylalanine Mustard
DNA alkylating agent
-
GC15571
SU 9516
A pro-apoptotic Cdk2/cyclin A inhibitor
-
GC17131
Streptozocin
链脲佐菌素; Streptozotocin; U 9889
Streptozocin 是一种有效的 DNA 甲基化抗生素,是一种天然存在的亚硝基酰胺,在实验模型中广泛用于产生糖尿病。 -
GC16866
Actinomycin D
放线菌素D,DACTINOMYCIN
阿克替诺霉素D(也称为达克替诺霉素)是一种从链霉菌属中分离出来的天然色胺肽,含有一个杂环色团和两个五元环戊肽内酯环。 -
GC17783
Veliparib dihydrochloride
维利帕尼二盐酸盐; ABT-888 dihydrochloride
An orally bioavailable inhibitor of PARP1 and PARP2 -
GC17386
YK-4-279
YK 4-279
YK-4-279 阻断 RNA Helicase A (RHA) 与 EWS-FLI1(致癌蛋白)的结合。 YK-4-279 诱导细胞凋亡并对各种癌细胞显示出抗增殖活性。 YK-4-279 有一个手性中心,它可以分成两种对映体。 YK-4-279可用于癌症研究。 -
GC14022
Voreloxin Hydrochloride
(3S-反式)-1,4-二氢-7-[3-甲氧基-4-(甲基氨基)-1-吡咯烷基]-4-氧代-1-(2-噻唑基)-1,8-萘啶-3-羧酸单盐酸盐,SNS-595 Hydrochloride; Vosaroxin Hydrochloride; AG 7352 Hydrochloride
Voreloxin Hydrochloride 是一流的拓扑异构酶 II 抑制剂,可嵌入 DNA 并诱导位点选择性 DNA DSB、G2 停滞和细胞凋亡。 -
GC13544
Voreloxin
SNS-595; Vosaroxin; AG 7352
An inhibitor of topoisomerase II -
GC10339
VAL-083
去水卫矛醇; Dianhydrodulcitol; Dianhydrogalactitol
VAL-083 是一种烷化剂,可在 DNA 上产生 N7 甲基化,具有抗肿瘤活性。 -
GC10649
TTP 22
TTP22;TTP-22
A CK2 inhibitor -
GC14473
Tipiracil hydrochloride
盐酸替吡嘧啶
A potent TPase inhibitor -
GC11298
TH-302
N,N'-双(2-溴乙基)二氨基膦酸(1-甲基-2-硝基-1H-咪唑-5-基)甲酯,TH 302,TH302,HAP-302,HAP302
A hypoxia-activated anticancer agent -
GC12181
TBB
4,5,6,7-四溴-1H-苯并三唑,NSC 231634; TBB (enzyme inhibitor);1H-Benzotriazole, 4,5,6,7-tetrabromo-
An inhibitor of CK2 -
GC14340
Tasquinimod
他喹莫德; ABR-215050
An orally-active anti-cancer compound -
GC17698
SJB2-043
An inhibitor of the USP1-UAF1 complex and SARS-CoV-2 PLpro
-
GC11455
Silvestrol
(1R,2R,3S,3AR,8BS)-6-[[(2S,3R,6R)-6-[(1R)-1,2-二羟基乙基]-3-甲氧基-1,4-二氧己环-2-基]氧基]-2,3,3A,8B-四氢-1,8B-二羟基-8-甲氧基-3A-(4-甲氧基苯基)-3-苯基-1H-环戊烯并[B]苯并呋喃-2-羧酸甲酯,(-)-Silvestrol
Silvestrol 是一种真核翻译起始因子 4A (eIF4A) 抑制剂,从 Agave americana Linn 中分离出来。Silvestrol 诱导自噬和半胱天冬酶介导的细胞凋亡。 -
GC12064
SB1317
14-甲基-20-氧杂-5,7,14,27-四氮杂四环[19.3.1.1(2,6).1(8,12)]二十七碳-1(25),2,4,6(27),8,10,12(26),16,21,23-十烯,TG02;SB 1317;TG 02;SB-1317;TG-02
A multi-kinase inhibitor -
GC10423
RG2833
RG 2833;RG-2833;RGFP-109;RGFP109;RGFP 109
An HDAC inhibitor -
GC14243
Resminostat hydrochloride
RAS2410 hydrochloride;4SC-201 hydrochloride;RAS 2410 hydrochloride;RAS-2410 hydrochloride
An orally bioavailable HDAC inhibitor -
GC16367
PSI-7977
索非布韦; GS-7977; PSI-7977
A prodrug form of PSI-7411 -
GC10995
PJ34
PJ-34;PJ 34
An inhibitor of poly (ADP-ribose) polymerases -
GC16379
PI-103 Hydrochloride
PI 103 hydrochloride;PI103 hydrochloride
A potent, cell-permeable PI3K inhibitor -
GC11324
PHA-767491
CAY10572;PHA767491;PHA 767491;CAY-10572;CAY 10572
A potent Cdc7 kinase inhibitor -
GC10556
PF-670462
4-[1-环己基-4-(4-氟苯基)-1H-咪唑-5-基]-2-嘧啶胺盐酸盐,PF 670462;PF670462
An inhibitor of the CK1 isoforms CK1ε and CK1δ -
GC17694
Pemetrexed disodium hemipenta hydrate
培美曲塞二钠水合物; LY231514 disodium hemipenta hydrate
Pemetrexed disodium hemipenta hydrate 是一种新型抗叶酸剂,LY231514 的五谷氨酸的 Ki 值分别为 1.3、7.2 和 65 nM,用于抑制胸苷酸合酶 (TS)、二氢叶酸还原酶 (DHFR) 和甘氨酰胺核糖核苷酸甲酰转移酶 (GARFT)。 -
GC14849
Paradol
姜酮酚; [6]-Gingerone; [6]-Paradol
A phenolic ketone with diverse biological activities -
GC14762
Palifosfamide
帕利伐米,Isophosphoramide mustard;IPM;ZIO-201
An active metabolite of ifosfamide -
GC16959
NVP-LCQ195
4-(2,6-二氯苯甲酰基氨基)-1H-吡唑-3-羧酸N-[1-(甲基磺酰基)哌啶-4-基]酰胺,LCQ-195;AT-9311;NVP LCQ195;LCQ 195;AT9311;AT 9311
NVP-LCQ195 (AT9311; LCQ195) 是 CDK1、CDK2、CDK3 和 CDK5 的小分子杂环抑制剂,IC50 为 1-42 nM。 -
GC17802
MK-4827
尼拉帕尼; MK-4827
An orally bioavailable PARP1/2 inhibitor -
GC11823
LY2835219 free base
阿贝西利,CDK4/6 dual inhibitor;LY 2835219 (free base);LY-2835219 (free base)
LY2835219 free base是 CDK4 和 CDK6 的强效选择性抑制剂,在非细胞实验中的 IC50 分别为 2nM 和 10nM。 -
GC11558
Levomefolate calcium
左旋甲状腺素钙
A biologically active form of folic acid -
GC16454
IWP-2
IWP 2
IWP-2 是Wnt信号通路中Porcupine 酶的特异性抑制剂,IC50值为 27 nM。 -
GC15853
Genz-644282
Genz644282;Genz 644282
An inhibitor of topoisomerase I -
GC16063
Flavopiridol
夫拉平度; HMR-1275; Alvocidib; L86-8275
An inhibitor of cyclin-dependent kinases -
GC16044
Emodin
大黄素; Frangula emodin
Natural CK2 inhibitor and ER agonist -
GC15250
DOXO-EMCH
INNO-206;Doxorubicin-EMCH;INNO 206
Prodrug of doxorubicin -
GC17837
DMAT
2-二甲基氨基-4,5,6,7-四溴苯并咪唑,Casein kinase II Inhibitor;CK2 Inhibitor
A cell-permeable inhibitor of CK2 -
GC17412
Deferasirox Fe3+ chelate
地拉罗斯铁螯合物
Deferasirox Fe3+ Chelate 是从专利 WO2003053986 中提取的铁螯合剂。