DNA Damage/DNA Repair(DNA损伤/DNA修复)
- MTH1(4)
- PARP(106)
- ATM/ATR(28)
- DNA Alkylating(22)
- DNA Ligases(3)
- DNA Methyltransferase(29)
- DNA-PK(28)
- HDAC(151)
- Nucleoside Antimetabolite/Analogue(145)
- Telomerase(13)
- Topoisomerase(142)
- tankyrase(5)
- Antifolate(32)
- CDK(235)
- Checkpoint Kinase (Chk)(28)
- CRISPR/Cas9(9)
- Deubiquitinase(64)
- DNA Alkylator/Crosslinker(71)
- DNA/RNA Synthesis(441)
- Eukaryotic Initiation Factor (eIF)(22)
- IRE1(22)
- LIM Kinase (LIMK)(11)
- TOPK(6)
- Casein Kinase(42)
- DNA Intercalating Agents(8)
- DNA/RNA Oxidative Damage(13)
- Cat.No. 产品名称 Information
- GC34356 Casein Kinase II Inhibitor IV Hydrochloride CaseinKinaseIIInhibitorIVHydrochloride是表皮角质形成细胞分化的小分子诱导剂。
- GC34355 SEL120-34A monohydrochloride A dual inhibitor of Cdk8 and Cdk19
- GC34354 GSK2643943A GSK2643943A is an inhibitor of deubiquitylating enzyme (DUB) with IC50 of 160 nM for USP20/Ub-Rho.
- GC34309 Cycloguanil D6 (Chlorguanide triazine D6) CycloguanilD6是Cycloguanil的氘代化合物标准品。
- GC34305 Bendamustine D4 (SDX-105 D4) BendamustineD4是Bendamustine的氘代化合物标准品。Bendamustine是一种DNA交联剂(DNAcrosslinker),能够导致DNA断裂,具有烷基化和抗代谢物的作用。
- GC34205 GSK2850163 hydrochloride GSK2850163hydrochloride是一个新型的肌醇需要酶-1α(IRE1α)抑制剂,它可抑制IRE1α的激酶活性和RNA酶活性,其IC50值分别为20和200nM。
- GC34204 JSH-150 JSH-150 is a highly selective and potent inhibitor of CDK9 with IC50 of 1 nM.
- GC34195 K-756 K-756是一种直接的选择性tankyrase(TNKS)抑制剂,抑制TNKS1和TNKS2的ADP-核糖基化活性,IC50分别为31和36nM。
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GC34169
Banoxantrone D12 dihydrochloride (AQ4N D12 dihydrochloride)
AQ4N-d12 dihydrochloride
Banoxantrone-d12 (AQ4N-d12) dihydrochloride 是氘标记的 Banoxantrone dihydrochloride。 Banoxantrone 是一种新型生物还原剂,可以还原为稳定的 DNA 亲和化合物 AQ4,它是一种有效的拓扑异构酶 II 抑制剂。 - GC34165 Corin Corin是组氨酸赖氨酸特异性去甲基化酶(LSD1)和组氨酸脱乙酰化酶(HDAC)的双重抑制剂,其对LSD1的Ki(inact)值为110nM,对HDAC1的IC50值为147nM。
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GC34163
Lerociclib (G1T38)
G1T38
G1T38 (Lerociclib) is a novel, potent, selective, and orally bioavailable CDK4/6 inhibitor with IC50 values of 0.001 μM, 0.002 μM and 0.028 μM for CDK4, CDK6 and CDK9 respectively. -
GC34156
Namitecan (ST-1968)
ST-1968
Namitecan (ST-1968) 是一种有效的拓扑异构酶 I 抑制剂,具有抗肿瘤特性。 -
GC34144
Karenitecin (Cositecan)
(4S)-4-乙基-4-羟基-11-(2-三甲基硅基)乙基)-1H-吡喃并[3',4':6,7]氮茚并[1,2-B]喹啉-3,14(4H,12H)-二酮,Cositecan; BNP 1350
Karenitecin (Cositecan) (Cositecan) 是一种拓扑异构酶 I 抑制剂,具有有效的抗癌活性。 -
GC34127
GDC-0575 dihydrochloride (ARRY-575 dihydrochloride)
ARRY-575 dihydrochloride; RG7741 dihydrochloride
A Chk1 inhibitor -
GC34124
(rel)-MC180295
(rel)-MC180295
MC180295 ((rel)-MC180295) is a novel potent and selective CDK9 inhibitor with an IC50 of 5 nM and is at least 22-fold more selective for CDK9 over other CDKs. -
GC34123
Deoxycytidine triphosphate (dCTP)
脱氧胞苷三磷酸; dCTP; 2′-Deoxycytidine-5′-triphosphate
脱氧胞苷三磷酸 (dCTP) (dCTP) 是一种核苷三磷酸,可用于 DNA 合成。 - GC34121 CC-115 hydrochloride A dual inhibitor of mTOR and DNA-PK
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GC34120
Niraparib R-enantiomer (MK 4827 (R-enantiomer))
MK 4827 (R-enantiomer)
Niraparib R-enantiomer (MK-4827 R-enantiomer) 是一种出色的 PARP1 抑制剂,IC50 为 2.4 nM。 -
GC34118
Trilaciclib (G1T28)
曲拉西利,G1T28
Trilaciclib (G1T28, G1T28-1) is a highly potent, selective and reversible cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor. Trilaciclib inhibits CDK4/cyclin D1 and CDK6/cyclin D3 with IC50 of 1 nM and 4 nM, respectively. -
GC34112
Ethynylcytidine (ECyD)
ECyD; TAS-106; 3'-C-Ethynylcytidine
A nucleoside analog with anticancer activity -
GC34111
NSC95682 (6-Bromo-2-hydroxy-3-methoxybenzaldehyde)
6-溴-2-羟基于-甲氧基苯甲醛,NSC95682
6-Bromo-2-hydroxy-3-methoxybenzaldehyde is a bromobenzaldehyde derivative that participates in the synthesis of (±)-norannuradhapurine. 6-Bromo-2-hydroxy-3-methoxybenzaldehyde is an IRE-1α inhibitor with an IC50 of 0.08 μM. -
GC34100
Lerociclib dihydrochloride (G1T38 dihydrochloride)
G1T38 dihydrochloride
Lerociclib dihydrochloride (G1T38 dihydrochloride) (G1T38 dihydrochloride) 是一种有效的选择性 CDK4/CDK6 抑制剂,对 CDK4/CyclinD1 和 CDK6/CyclinD3 的 IC50 分别为 1 nM 和 2 nM。 -
GC34090
Acelarin (NUC-1031)
N-(2'-脱氧-2',2'-二氟-P-苯基-5'-胞苷酰)-L-丙氨酸苄酯,NUC-1031
A prodrug form of gemcitabine -
GC34087
Trilaciclib hydrochloride (G1T28 hydrochloride)
曲拉西利双盐酸盐,G1T28 hydrochloride
Trilaciclib hydrochloride (G1T28 hydrochloride) (G1T28 hydrochloride) 是一种 CDK4/6 抑制剂,对 CDK4 和 CDK6 的 IC50 分别为 1 nM 和 4 nM。 -
GC34086
SJG-136 (NSC-694501)
NSC-694501
SJG-136 (NSC-694501) 是一种 DNA 交联剂,对于 pBR322 DNA 的 XL50 为 45 nM。 SJG-136 (NSC-694501) 具有有效的抗肿瘤活性。 -
GC34085
Banoxantrone dihydrochloride (AQ4N dihydrochloride)
AQ4N dihydrochloride
Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种缺氧活化拓扑异构酶 II 抑制剂,AQ4N 以非共价方式与 DNA 结合,促进缺氧和缺氧肿瘤细胞的抗肿瘤活性。 - GC34083 EOAI3402143 EOAI3402143 is a dose-dependent inhibitor of Usp9x, Usp24 and Usp5 that increases tumor cell apoptosis, and fully blocks or regresses myeloma tumors in mice.
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GC34071
Pamiparib (BGB-290)
帕米帕利,BGB-290
A PARP1 and PARP2 inhibitor -
GC34059
Atuveciclib Racemate (BAY-1143572 Racemate)
BAY-1143572 Racemate
Atuveciclib (BAY-1143572) is potent and highly selective PTEFb/CDK9 inhibitor with IC50 values of 13 nM for CDK9/CycT and the ratio of IC50 values for CDK2/CDK9 is about 100. Outside the CDK family, It inhibits GSK3 kinase with IC50 values of 45 nM and 87 nM for GSK3α and GSK3β respectively. - GC34056 NVP-2 A Cdk9/cyclin T1 complex inhibitor
- GC33959 Nucleoside-Analog-2 Nucleoside-Analog-2是针对丙型肝炎病毒(HCV)复制的4'-叠氮胞苷类似物。
- GC33956 Nucleoside-Analog-1 Nucleoside-Analog-1是抗病毒核苷R1479的类似物,用于HCV看病毒核苷类似物的合成。
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GC33944
Pseudothymidine (5-Methyl-2'-Deoxypseudouridin)
5-(2-脱氧-BETA-D-赤式-呋喃戊糖基)-1-甲基-2,4(1H,3H)-嘧啶二酮,5-Methyl-2'-Deoxypseudouridin
Pseudothymidine (5-Methyl-2'-Deoxypseudouridin) 是胸苷的 C-核苷类似物。 -
GC33662
Isoguanine
异鸟嘌呤
An isomer of guanine -
GC33577
7-Aminoactinomycin D (7-AAD)
7-氨基放线菌素D; 7-AAD
7-Aminoactinomycin D是放线菌素D的荧光衍生物,选择性地与DNA的GC区域结合。
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GC33496
2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine)
6-羟基-2-氨甲基嘌呤,N2-methylguanine
2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) (N2-Methylguanine) 是一种修饰的核苷。 -
GC33494
Deoxypseudouridine
脱氧假尿苷
Deoxypseudouridine是一种核苷酸类似物。 - GC33430 2'-Deoxypseudoisocytidine 2'-Deoxypseudoisocytidine是一个核苷类似物。
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GC33426
Rocaglamide (Rocaglamide A)
楝酰胺,Rocaglamide A; Roc-A
Rocaglamide (Rocaglamide A) 是从 Aglaia 属(楝科)中分离出来的。 -
GC33420
BAY-1895344
BAY 1895344
An ATR inhibitor -
GC33411
MB-7133
4-氨基-1-[5-O-[(2R,4S)-2-氧代-4-(4-吡啶基)-1,3,2-二氧磷杂环己烷-2-基]-BETA-D-呋喃阿拉伯糖基]-2(1H)-嘧啶酮
MB-7133是一种DNAsynthesis抑制剂。 - GC33406 B I09 BI09是IRE-1核糖核酸酶的一个抑制剂,其IC50值为1230nM。
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GC33404
KU 59403
KU59403是ATM的一个有效抑制剂,其IC50值为3nM。
- GC33395 HDAC-IN-5 HDAC-IN-5是组蛋白去乙酰化酶(HDAC)的一个抑制剂。
- GC33392 CHK-IN-1 CHK-IN-1是一种CHK1和CHK2的抑制剂,具有抗增殖作用。
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GC33389
LMP744 (MJ-III65)
MJ-III65; NSC706744
LMP744 (MJ-III65) (MJ-III65) 是一种 DNA 嵌入剂和拓扑异构酶 I (Top1) 抑制剂,具有抗肿瘤活性。 - GC33373 LY309887 LY309887是一种有效的二氢叶酸还原酶(GARFT)抑制剂,Ki值为6.5nM,具有抗肿瘤活性。
- GC33366 CDK8-IN-4 CDK8-IN-4是CDK8的抑制剂,来自专利WO2014090692A1,化合物实例16,IC50值为0.2nM。
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GC33360
Roniciclib (BAY 1000394)
BAY 1000394
Roniciclib (BAY 1000394) 是一种可口服的泛细胞周期蛋白依赖性激酶 (CDK) 抑制剂,对 CDK1、CDK2、CDK3、CDK4、CDK7 和 CDK9 的 IC50 为 5-25 nM。 - GC33358 WD2000-012547 WD2000-012547是一种选择性的PARP-1抑制剂,pKi为8.221。