40
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4327 |
Prexasertib dihydrochloride
LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368 |
Apoptosis; Chk; S6 Kinase | Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling |
Prexasertib dihydrochloride (LY2606368) 是一种选择性的,ATP 竞争性的细胞周期检测点激酶 1 抑制剂,Ki 为 0.9 nM,IC50为 <1 nM。它抑制 CHK2(IC50=8 nM) 和 RSK1 (IC50=9 nM)。它引起双链 DNA 断裂和复制突变,导致细胞凋亡,有抗肿瘤活性。 | |||
T12516 |
Polyinosinic-polycytidylic acid sodium
双链聚肌胞,Poly(I:C) sodium |
Apoptosis; Others; TLR | Apoptosis; Immunology/Inflammation; Others |
Polyinosinic-polycytidylic acid sodium (Poly(I:C) sodium) 是双链 RNA 的合成类似物,是TLR3和视黄酸诱导型基因 I 受体激动剂。它可以用作疫苗佐剂,直接触发癌细胞发生凋亡,还增强先天性和适应性免疫反应,并改变肿瘤的微环境。 | |||
T4310 |
Prexasertib
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 |
Apoptosis; Chk | Apoptosis; Cell Cycle/Checkpoint |
Prexasertib (LY2606368) 是一种具有潜在抗肿瘤活性的检查点激酶 1 抑制剂。它可引起双链 DNA 断裂和复制突变,导致细胞凋亡。 | |||
T18883 |
2-Di-1-ASP
|
Others | Others |
2-Di-1-ASP 是单苯乙烯基染料,对 G-四链体和双链 DNA 具有选择性。它普遍用作双链 DNA 的线粒体染色和凹槽结合荧光探针。 | |||
T23171 |
Polyinosinic-polycytidylic acid
Poly(I:C),聚胞苷酸 |
TLR | Immunology/Inflammation |
Polyinosinic-polycytidylic acid (Poly(I:C)) 是一种双链 RNA (dsRNA),是一种 TLR3 激动剂。Polyinosinic-polycytidylic acid 可以诱导哺乳动物天然免疫。 | |||
T38709 |
PFM39
|
||
PFM39, a Mirin analog, is a potent and selective inhibitor of MRE11 exonuclease activity, specifically targeting the inhibition of phosphate rotation necessary for double-stranded DNA (dsDNA) exonuclease function. Importantly, PFM39 does not inhibit Thermotoga maritima Mre11 (TmMre11) or human MRE11/MRN complex endonuclease activity. | |||
T19836 |
2-Aminopurine
|
DNA/RNA Synthesis; PKA | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors |
2-Aminopurine 是一种鸟苷和腺苷的荧光类似物,是基于荧光衰变的 DNA 结构探针。当它插入寡核苷酸后,其荧光会通过与天然碱基堆积而被高度淬灭。它可用于核酸的结构和动力学的探测。 | |||
T8637 |
DMNB
6-Nitroveratraldehyde,6-硝基藜芦醛 |
DNA-PK | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
DMNB (6-Nitroveratraldehyde) 可用于合成no-carrier-added 6-[18F]fluoro-L-DOPA (6-FDOPA)。它可用于研究多巴胺能系统的PET。 | |||
T4434 |
Tirapazamine
Tirazone,Win59075,SR4233,替拉扎明,SR259075 |
Others | Others |
Tirapazamine (Win59075) 是抗癌剂,对实体瘤中的缺氧细胞具有选择性细胞毒性,促使 DNA 中的单链和双链断裂,碱基损伤和细胞死亡。 | |||
TD0003 |
CelGreen nucleic acid gel stain *10,000× concentrate in water*
|
Others | Others |
CelGreen 是一种具有独特参与性的荧光染料,可与所有 dsDNA 双螺旋沟区域结合。在游离状态下,侧链和 CelGreen 发出微弱的荧光,但一旦与双链DNA 结合,荧光就会大大增强。因此,CelGreen 的荧光信号强度与双链DNA 的量有关,可以根据荧光信号检测PCR 系统中双链DNA 的量。 | |||
T67931 |
[Tyr3]Octreotate
|
Others | Others |
[Tyr3]Octreotate 是一个含有8个氨基酸的长肽化合物,是具有共价键DOTA 双功能螯合剂。[Tyr3]Octreotate 与SSR2活性的NETs 的跨膜受体结合,并通过内吞作用主动运输到细胞中,可能会增加所需的双链DNA 断裂,是治疗肿瘤的潜在药物。 | |||
T19003 |
HOE-S 785026 trihydrochloride
meta-Hoechst trihydrochloride,Meta-Hoechst trihydrochloride,HOE-S 785026 trihydrochloride (132869-83-1 free base) |
||
HOE-S 785026 trihydrochloride 是一种活细胞标记染料,通过结合 DNA 双链中的小沟而结合核酸。 HOE-S 785026 trihydrochloride 倾向于结合富含 A/T 的 DNA 链(富含 A/T 的双链 DNA 使荧光强度显著增强)。HOE-S 785026 trihydrochloride 可穿过细胞膜,与活细胞或固定细胞结合。HOE-S 785026 trihydrochloride 的荧光强度随着溶液 pH 升高而增加。 | |||
T16283 | Neocarzinostatin | 5-HT Receptor | GPCR/G Protein; Neuroscience |
Neocarzinostatin is an effective DNA-damaging, anti-tumor antibiotic. It recognizes double-stranded DNA bulge and induces DNA double strand breaks (DSBs). Neocarzinostatin leads to apoptosis. Neocarzinostatin has potential for EpCAM-positive cancer treatment. | |||
T39122 |
Inclisiran
ALN-PCSsc |
||
Inclisiran (ALN-PCSsc) is a double-stranded small interfering RNA (siRNA) compound that effectively suppresses PCSK-9 transcription. It proves promising in the investigation of hyperlipidemia and cardiovascular disease (CVD). | |||
TD0003L |
CelGreen nucleic acid gel stain *10,000× concentrate in DMSO*
|
||
CelGreen is a fluorescent dye with a unique involvement that binds to all dsDNA double helix sulcus regions.In the free state, the side strand and CelGreen emit weak fluorescence, but the fluorescence is greatly enhanced once they are combined with the do | |||
T76109 | Nuclease S1 | ||
Nuclease S1 是一种特异性的核酸内切酶,可降解单链 DNA (ssDNA) 和 RNA。Nuclease S1 还可以去除双链 DNA 中突出的单链末端。 | |||
T69283 | Amikhellin HCl | ||
Amikhellin HCl, an antimitotic drug, is a synthetic water-soluble derivative of khellin, an alkaloid extracted from seeds of Ammi Visnaga. Amikhellin has been used so far mostly as a vasodiator. Amikhellin binds to double-stranded DNA by an intercalation process. It inhibits the DNA-polymerase from murine sarcoma leukemia virus. | |||
T36298 |
Tyrocidine Complex
|
||
Tyrocidine complex is a mixture of cyclic decapeptides originally isolated from B. brevis. It is active against Gram-positive and Gram-negative bacteria. It forms a complex with single- and double-stranded DNA to inhibit RNA synthesis. | |||
T76160 | Nuclease P1 | ||
Nuclease P1 (核酸酶 P1) 是一种单链特异性核酸内切酶,它将核酸水解为 5'-单核苷酸,并切割双链核酸的单链区域。Nuclease P1 是分子生物学领域著名的单链特异性核酸酶之一,广泛应用于制药和食品行业。 | |||
T38804 | Patisiran sodium | ||
Patisiran sodium is a double-stranded small interfering RNA (siRNA) that selectively targets a specific sequence within the transthyretin (TTR) messenger RNA (mRNA). By doing so, it effectively blocks the hepatic synthesis of both mutant and wild-type TTR. Patisiran sodium has significant applications in the field of hereditary TTR amyloidosis research. | |||
T82995 | Antiviral agent 33 | ||
Antiviralagent 33(化合物 1c)作为一种抗双链 DNA (dsDNA) 病毒的抑制剂,针对 VACV 和 AdV5 表现出的IC50值分别是 0.0790 µM 和 0.1572 µM,同时展现了潜在的口服给药能力。 | |||
T69669 | Camsirubicin HCl | ||
Camsirubicin, also known as GPX-150, MNPR-201, and CNDO1011, is a synthetic non-cardiotoxic analogue of the anthracycline antibiotic doxorubicin with potential antineoplastic activity. Anthracycline analogue GPX-150 intercalates DNA and impedes the activity of topoisomerase II, inducing single and double-stranded breaks in DNA; inhibiting DNA replication and/or repair, transcription, and protein synthesis; and activating tumor cell apoptosis. | |||
T68895 |
CBP-93872
|
||
CBP-93872 is a G2 checkpoint inhibitor. CBP-93872 specifically abrogates the DNA double-stranded break (DSB)-induced G2 checkpoint through inhibiting maintenance. CBP-93872 is an inhibitor of maintenance of the DSB-specific G2 checkpoint and thus might be a strong candidate as the basis for a drug that specifically sensitizes p53-mutated cancer cells to DSB-inducing DNA damage therapy. | |||
T79925 |
T4 UvsX Recombinase
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
T4 UvsX Recombinase 促进双链DNA模板上DNA复制的启动,通过催化模板DNA与同源单链DNA引物间的突触形成。此酶显著增强了T4 DNA聚合酶全酶在线性单链DNA模板上进行的回跳(发夹引物)DNA合成反应。 | |||
T69024 |
Homidium Cl
|
||
Homidium Chloride is the chloride salt of ethidium (a fluorochrome), Ethidium Chloride intercalates within double-stranded nucleic acids, particularly DNA. In molecular biology, the bromide salt of ethidium is used to detect and visualize DNA after electrophoresis or in cytochemical preparations. In veterinary pharmacology, it is used as a trypanosomicide. Ethidium bromide and chloride are toxic substances and potent noncompetitive antagonists of the nicotinic acetylcholine receptor. | |||
T74248 |
AS-Inclisiran
|
||
AS-Inclisiran为Inclisiran的反义链。Inclisiran(ALN-PCSsc)为双链小干扰RNA(siRNA)分子,目的在于抑制PCSK-9的转录,适用于高脂血症及心血管疾病(CVD)的研究。 | |||
T38620 |
Prexasertib dimesylate
LY2606368 dimesylate |
||
Prexasertib dimesylate (LY2606368 dimesylate) is a highly selective ATP-competitive second-generation inhibitor of checkpoint kinase 1 (CHK1). With a K i of 0.9 nM and an IC 50 of <1 nM, Prexasertib dimesylate effectively inhibits CHK2 (IC 50 = 8 nM) and RSK1 (IC 50 = 9 nM). Its mechanism of action involves inducing double-stranded DNA breakage and replication catastrophe, ultimately leading to apoptosis. Moreover, Prexasertib dimesylate demonstrates potent anti-tumor activity. | |||
T74876 |
GalNAc unconjugated/naked Inclisiran
|
||
GalNAc unconjugated/naked Inclisiran 是一种未偶联GalNAc的双链小干扰RNA (siRNA) 分子,具有抑制PCSK-9转录功能。该化合物主要应用于高脂血症及心血管疾病(CVD)的研究领域。 | |||
T79923 |
T7 RNA polymerase
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
T7 RNA polymerase是一种由大肠杆菌表达的聚合酶,由T7噬菌体的RNA聚合酶基因编码。它在合成mRNA体外转录(IVT)过程中显示出高度专一性。T7 RNA polymerase能在Mg2+的作用下,针对含有T7启动子序列的单链或双链DNA模板,使用NTP作为底物进行RNA合成,产生的RNA与DNA模板的启动子下游区域互补。 | |||
T74249 |
AS(3n-2)-Inclisiran
|
||
AS(3n-2)-Inclisiran 是 Inclisiran 的反义链,其在 2 bp 的间隔后有3n 个随机位点。Inclisiran 是一种双链小干扰 RNA (siRNA) 分子,可抑制PCSK-9的转录。 | |||
T4310L2 |
Prexasertib mesylate
LY-2606368,LY2606368,LY 2606368 |
||
Prexasertib is a potent and selective Chk1/Chk2 inhibitor. Prexasertib increases the effectiveness of conventional therapy in B-/T- cell progenitor acute lymphoblastic leukemia. LY2606368 causes replication catastrophe and antitumor effects through CHK1-d | |||
T35270 |
YO-Pro 1
YO-Pro1,YO-Pro-1 |
||
YO-Pro 1 是一种由苯并恶唑和喹啉环通过连接体连接而成的菁染料,在水中几乎没有荧光,但其荧光在插入双链DNA后大大增强,成为DNA浓度测定的基础,Ex/Em (结合DNA) = 491/509 nm。YO-Pro 1 可用于鉴定凋亡细胞。 | |||
T83217 |
Abetimus
LJP 394 free base |
||
Abetimus (LJP 394 free base)为一种由四个双链DNA (dsDNA) 寡核苷酸构成的免疫抑制剂,其作用机制为通过交联B细胞表面的抗dsDNA抗体,从而降低体内抗dsDNA抗体水平,具备作为系统性红斑狼疮研究工具的潜力。 | |||
T83298 |
5'6-FAM-GGUGAAAGACGAUGGACAATT,UUGUCCAUCGUCUUUCACCTT
|
||
5'6-FAM-GGUGAAAGACGAUGGACAATT,UUGUCCAUCGUCUUUCACCTT 是一种由荧光分子5'6-FAM修饰的双链核糖核酸。其中,5'6-FAM实际为5-FAM与6-FAM的混合物,其激发和发射光谱的特征值分别为Ex/Em= 490 nm/520 nm。 | |||
T73674 | Poly (I:C):Kanamycin (1:1) | ||
Poly (I:C):Kanamycin (1:1) 是一种 Poly (I:C) 与卡那霉素 (kanamycin) 以 1:1 比例混合得到的化合物。Poly (I:C) 为双链 RNA 的合成模拟物,充当 TLR3 受体的激动剂,而卡那霉素则能够增强 Poly (I:C) 的稳定性。 | |||
T11338 |
Furamidine
DB75,NSC 305831 |
Others | Others |
Furamidine is also a selective and cell-permeable protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 9.4 μM. Furamidine is selective for PRMT1 over PRMT5, PRMT6, and PRMT4 (CARM1) (IC50s of 166 μM, 283 μM, and >400 μM, respectively). Furamidine (DB75) is abisbenzamidine derivative and an antiparasite agent. Furamidine is a potent, reversible and competitive tyrosyl-DNA phosphodiesterase 1 (TDP-1) inhibitor. Inhibition of TDP-1 by Furamidine is effective both with single- and ... | |||
T79539 |
Topoisomerase II inhibitor 16
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseII inhibitor 16(化合物CT3)是一个选择性的、口服活性的、能够穿透血脑屏障的,并对锥虫拓扑异构酶 II(trypanosomaltopoisomeraseII)产生不可逆抑制的化合物,能够稳定DNA双螺旋与酶之间的复合物。该抑制剂在恰加斯病的研究中显示出潜在应用价值。 | |||
T63152 |
Prexasertib Mesylate Hydrate
|
||
Prexasertib Mesylate Hydrate (LY2606368 Mesylate Hydrate) 是一种 ATP 竞争性的、选择性的第二代细胞周期检测点激酶 1 (CHK1) 抑制剂 (IC50<1 nM, Ki: 0.9 nM)。Prexasertib Mesylate Hydrate 对 CHK2 (IC50: 8 nM) 和 RSK1 (IC50: 9 nM) 表现出抑制作用。Prexasertib Mesylate Hydrate 能够导致双链 DNA 断裂和复制突变,诱导细胞凋亡,并表现出有效的抗肿瘤作用。 | |||
T74052 | Polyinosinic-polycytidylic acid potassium | ||
Polyinosinic-polycytidylic acid potassium (Poly(I:C) potassium) 是双链 RNA 的合成类似物,是一种TLR3和视黄酸诱导型基因 I 受体 (RIG-I 和MDA5) 的激动剂。Polyinosinic-polycytidylic acid potassium 可以用作疫苗佐剂,以增强先天性和适应性免疫反应,并改变肿瘤的微环境,还可以直接触发癌细胞发生凋亡 (Apoptosis)。 | |||
T74067 | Poly (I:C):Kanamycin (1:1) (sodium) | ||
Poly (I:C):Kanamycin (1:1) sodium 是 Poly (I:C) 和 Kanamycin 的等比例复合物。Poly(I:C) sodium 是双链 RNA 的合成类似物,是一种TLR3和视黄酸诱导型基因 I 受体 (RIG-I 和MDA5) 的激动剂。Poly(I:C) sodium 可以用作疫苗佐剂,增强先天性和适应性免疫反应,并诱导癌细胞凋亡。Kanamycin 是一种具有口服活性的抗菌剂(革兰氏阴性/阳性细菌),可抑制易位并通过与 70 S 核糖体亚基结合引起错误编码。Kanamycin 对结核分枝杆菌(敏感和耐药)和肺炎克雷伯菌均表现出良好的抑制活性,可用于结核病和肺炎的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20041 |
2'-Deoxyadenosine
2'-脱氧腺苷,NSC-141848,NSC141848,NSC 141848 |
Endogenous Metabolite | Metabolism |
2'-Deoxyadenosine (NSC-141848) 是核苷腺苷的一种衍生物,能够与双链 DNA 中的脱氧胸苷配对。 | |||
T13592 |
Calf thymus DNA
DNA from calf thymus, Thymonucleic acid |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Calf thymus DNA (DNA from calf thymus, Thymonucleic acid) 是一种从牛胸腺中提取出来的高质量双链模板DNA,可广泛应用于DNA 结合抗癌剂和调节DNA 结构和功能的DNA 结合剂的研究。 | |||
T6228 |
Irinotecan
CPT-11,Topotecin,伊立替康,(+)-Irinotecan |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Irinotecan (CPT-11) 是喜树碱的衍生物,是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂。Irinotecan 通过与 Topo I 复合物结合来阻止 DNA 链的重新连接,并导致双链 DNA 断裂和细胞死亡,具有抗肿瘤活性。 | |||
T4809 |
Pyrimidine
嘧啶,Metadiazine |
Others; Endogenous Metabolite | Metabolism; Others |
Pyrimidine (Metadiazine) 是内源性代谢产物的一种。 |