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
-
GC12332
NU 7026
2-(4-吗啉基)-4H-萘并[1,2-B]吡喃-4-酮,LY293646
Inhibitor of DNA-dependent protein kinase -
GC17716
Oxaliplatin
奥沙利铂
奥沙利铂(Oxaliplatin)是一种用于治疗癌症的细胞毒性化疗药物。
-
GC15866
Capecitabine
卡培他滨
A prodrug of 5-fluorouracil -
GC12044
Trovafloxacin mesylate
曲伐沙星甲磺酸盐
A topoisomerase IV and DNA gyrase inhibitor -
GC14663
Viomycin
紫霉素
紫霉素是一种针对分枝杆菌的强效抗生素。当将紫霉素添加到积极参与多肽合成的纯化内源性大肠杆菌多核糖体中时,紫霉素会迅速抑制多肽链的延伸。 -
GC17186
Acyclovir
阿昔洛韦
Acyclovir是一种强效的口服抗病毒药物。Acyclovir具有抗疱疹活性,对 HSV-1 和 HSV-2 的 IC50 值分别为 0.85μM 和 0.86μM。Acyclovir诱导细胞周期紊乱和细胞凋亡。 -
GC17400
R547
[4-氨基-2-[(1-甲磺酰基哌啶-4-基)氨基]嘧啶-5-基](2,3-二氟-6-甲氧基苯基)甲酮
A selective Cdk inhibitor -
GC10842
LEE011
瑞博西尼; LEE011
A selective cyclin D1/CDK4 and cyclin D3/CDK6 inhibitor -
GC16425
Flavopiridol hydrochloride
(-)-2-(2-氯苯基)-5,7-二羟基-8-[(3S,4R)-3-羟基-1-甲基-4-哌啶基]-4H-1-苯并吡喃-4-酮盐酸盐,Alvocidib Hydrochloride; L86-8275 Hydrochloride; HMR-1275 Hydrochloride
An inhibitor of cyclin-dependent kinases -
GC15741
LY2603618
LY2603618; IC-83
A Chk1 inhibitor -
GC10196
ETP-46464
ATM Inhibitor III, ATR Inhibitor III
An ATR inhibitor -
GC16489
CP-466722
An ATM kinase inhibitor
-
GC14526
CGK733
ATM/ATR Kinase Inhibitor
An anticancer compound -
GC11548
Tankyrase Inhibitors (TNKS) 49
TNKS 49;TNKS49;TNKS-49
Tankyrase inhibitor -
GC15041
Tankyrase Inhibitors (TNKS) 22
TNKS 22;TNKS22;TNKS-22
Tankyrase inhibitor -
GC16268
Purvalanol B
(2R)-2-[[6-[(3-氯-4-羧基苯基)氨基]-9-(1-甲基乙基)-9H-嘌呤-2-基]氨基]-3-甲基-1-丁醇,NG 95; NG95; NG-95
A CDK inhibitor -
GC10322
Tubastatin A HCl
TubastatinA盐酸盐,TSA HCl;Tubastatin A hydrochloride
A potent HDAC6 inhibitor -
GC17648
Dinaciclib(SCH727965)
(2S)-1-[3-乙基-7-[[(1-氧代-3-吡啶基)甲基]氨基]吡唑并[1,5-A]嘧啶-5-基]-2-哌啶乙醇,SCH 727965
A CDK inhibitor -
GC13070
Cytarabine
阿糖胞苷; Cytosine β-D-arabinofuranoside; Cytosine Arabinoside; Ara-C
Cytarabine(Ara-C)是一种胞嘧啶类似物,主要抑制DNA聚合酶的功能来阻断DNA合成。 -
GC15739
CHIR-124
4-[((3S)-1-氮杂双环[2,2,2]辛-3-基)氨基]-3-(1H-苯并咪唑-2-基)-6-氯喹啉-2(1H)-酮
A selective Chk1 inhibitor -
GC13671
Busulfan
白消安
An alkylating antineoplastic agent -
GC12865
BMS265246
A cell-permeable inhibitor of Cdk1 and Cdk2
-
GC13803
Triflurdine (Viroptic)
曲氟尿苷; Trifluorothymidine; 5-Trifluorothymidine; TFT
A thymidine analog that inhibits DNA synthesis -
GC15392
Triciribine
曲西瑞宾,API-2; NSC 154020; TCN
A selective, potent inhibitor of Akt activation -
GC16084
Teniposide
替尼泊苷; VM26
A topoisomerase II poison -
GC16970
Rifaximin (Xifaxan)
利福昔明
An antibiotic and PXR agonist -
GC15588
PHA-848125
PHA-848125
An inhibitor of Cdks -
GC14075
Nocodazole
诺考达唑
Nocodazole是一种抗有丝分裂药物,是一种快速可逆的微管聚合抑制剂,在无细胞试验中抑制Abl,Abl(E255K)和Abl(T315I),IC50值分别为0.21μM,0.53μM和0.64μM。 -
GC16374
MK-8776(SCH-900776)
6-溴-3-(1-甲基-1H-吡唑-4-基)-5-(3R)-3-哌啶基吡唑并[1,5-A]嘧啶-7-胺,MK-8776
A selective Chk1 inhibitor -
GC16805
Gemcitabine
吉西他滨; LY 188011
An anticancer nucleoside analog
-
GC14404
CX-5461
CX 5461;CX5461
CX-5461是一种具口服活性的rRNA合成抑制剂,在HCT-116、A375和MIA PaCa-2细胞中,它抑制RNA聚合酶(RNA Pol)I驱动的rRNA转录,IC50分别为142、113和54nM。 -
GC12054
KU-60019
KU60019;KU 60019
A potent ATM kinase inhibitor -
GC15421
Palbociclib (PD0332991) Isethionate
帕博西尼羟乙基磺酸盐; PD 0332991 isethionate
Palbociclib (PD 0332991) isethionate 是一种具有口服活性的选择性 CDK4 和 CDK6 抑制剂,IC50 值分别为 11 和 16 nM。 Palbociclib (PD0332991) Isethionate 具有有效的抗增殖活性,可诱导癌细胞的细胞周期停滞,可用于 HR 阳性和 HER2 阴性乳腺癌和肝细胞癌的研究。 -
GC15819
Bleomycin Sulfate
硫酸博来霉素
博来霉素由链霉菌产生。 -
GC13037
CX-4945 (Silmitasertib)
CX 4945;CX4945
A potent, orally bioavailable CK2 inhibitor -
GC12438
AZD-5438
4-[2-甲基-1-异丙基-1H-咪唑-5-基]-N-[4-(甲磺酰基)苯基]-2-嘧啶胺,AZD 5438;AZD5438
A potent inhibitor of CDKs -
GC10970
WP1130
WP 1130; WP-1130
A deubiquitinase inhibitor -
GC11908
Cisplatin
顺铂; cis-Platinum; CDDP; cis-Diaminodichloroplatinum
顺铂是最好的、最早的基于金属的化疗药物之一,用于治疗广泛的实体癌症,如睾丸癌、卵巢癌、膀胱癌、肺癌、宫颈癌、头颈部肿瘤和胃癌等。 -
GC15134
Fludarabine Phosphate (Fludara)
磷酸氟达拉滨; NSC 118218 phosphate
A prodrug form of fludarabine and 2-fluoro-ara-ATP -
GC17935
PD 0332991 (Palbociclib) HCl
帕布昔利布盐酸盐,PD0332991;PD-0332991;PD 0332991
PD 0332991 作为 CDK4 和 CDK6 激酶的口服活性强效和高选择性抑制剂,可以在低纳摩尔浓度下阻断 pRb 磷酸化并随后在敏感细胞系中诱导 G1 期停滞。 -
GC11251
NU7441 (KU-57788)
8-(4-二苯并噻吩基)-2-(4-吗啉基)-4H-1-苯并吡喃-4-酮,KU 57788; NU-7441;KU57788;NU7441;NU 7441
NU7441 (KU-57788)是一种高效的选择性DNA依赖性蛋白激酶(DNA-PK)抑制剂,IC50为13nM。NU7441还抑制磷脂酰肌醇3-激酶(PI3K)和哺乳动物雷帕霉素靶蛋白(mTOR),IC50分别为5.0和1.7μM。 -
GC16822
LY2835219
Abemaciclib; LY2835219 methanesulfonate
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。 -
GC14346
KU-0060648
A dual inhibitor of DNA-PK and PI3K
-
GC10293
VE-821
3-氨基-6-[4-(甲基磺酰基)苯基]-N-苯基-2-吡嗪甲酰胺
An inhibitor of ATR
-
GC10546
AZD7762
3-[(氨基羰基)氨基]-5-(3-氟苯基)-N-(3S)-3-哌啶基-2-噻吩羧胺
A selective checkpoint kinase inhibitor -
GC15870
AT7519
4-[(2,6-二氯苄基)氨基]-N-4-哌啶1H-吡唑-3-羧胺,AT7519M
A Cdk inhibitor -
GC13690
BS-181 HCl
A selective Cdk7 inhibitor
-
GC12292
Ofloxacin
氧氟沙星; Hoe-280
A fluoroquinolone antibiotic -
GC15047
PHA-793887
3-甲基-N-[1,4,5,6-四氢-6,6-二甲基-5-[(1-甲基-4-哌啶基)甲酰基]吡咯并[3,4-C]吡唑-3-基]丁酰胺
A CDK inhibitor -
GC11114
Moxifloxacin HCl
莫西沙星盐酸盐; BAY 12-8039
A fluoroquinolone antibiotic