66
13
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21899 |
Misonidazole
SR-1354,SR1354,Ro 7-0582 |
GPX | oxidation-reduction |
Misonidazole 是一种缺氧肿瘤细胞放射增敏剂,具有抗菌活性。 | |||
T2046 |
Nimorazole
Nimorazol,Nitrimidazine,尼莫唑,K-1900,Naxogin,尼莫拉唑 |
Others; Antibiotic; Parasite | Microbiology/Virology; Others |
Nimorazole (Nimorazol) 是一种 2-硝基咪唑,是一种低氧细胞辐射敏化剂。它具有抗感染,抗滴虫等原生动物的作用。它有头颈癌的研究潜力。 | |||
T1478 |
Ondansetron hydrochloride dihydrate
盐酸昂丹司琼,SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ondansetron hydrochloride dihydrate (GR 38032) 是5- HT3受体拮抗剂,可治疗化疗后的恶心和呕吐,有抗焦虑和抗精神病作用。 | |||
T19957 |
Bismaleimide
XU 292A,XU-292A,XU292A |
Others | Others |
Bismaleimide (XU 292A) 具有抗热性、抗氧化性、抗辐射性,可用于制备电器绝缘材料、耐磨材料、增强塑料添加剂、砂轮粘结剂等。 | |||
T2068 |
(Rac)-LB-100
|
Phosphatase | Metabolism |
LB-100 是一种新型蛋白磷酸酶 2A (PP2A) 抑制剂,可使恶性脑膜瘤细胞对放射治疗效果敏感。 | |||
T20109 |
Cystamine dihydrochloride
|
Others | Others |
Cystamine dihydrochloride 是一种辐射防护剂。它还可以防止四氯化碳肝损伤。 | |||
T0698 |
Dioxybenzone
UV-24,二羟苯宗,Benzophenone-8,2,2'-Dihydroxy-4-methoxybenzophenone,Dioxybenzon,Cyasorb UV 24,Advastab 47 |
Others | Others |
Dioxybenzone (Benzophenone-8) 是一种能够阻断 UVB 和短波 UVA 紫外线照射的有机试剂。 | |||
T24184 |
Itasetron
DAU6215CL,UNII-00S0D0OEKR,U-98079A,U 98079A,DAU 6215CL |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Itasetron (U 98079A) 是一种5-羟色胺3受体拮抗剂,可用于预防大鼠与年龄有关的记忆缺陷。Itasetron 在癌症化疗和放疗动物模型中的止吐活性,可用于研究健忘症。 | |||
T15943 |
M443
|
p38 MAPK; Chk | Cell Cycle/Checkpoint; MAPK |
M443 是一种高效的 MRK 小分子抑制剂,抑制辐射诱导的 p38 和 Chk2 的激活,可用于研究癌症。 | |||
TP1024 |
Rusalatide acetate (497221-38-2 free base)
Rusalatide acetate,TP508 amide acetate |
Others | Others |
Rusalatide acetate (TP508 amide acetate) 是一种再生肽,可诱导干细胞再生修复,保护隐窝完整性,减缓辐照引起的胃肠道损伤。 | |||
T12019 |
Methylproamine
|
Others | Others |
Methylproamine 是一种与DNA 结合的辐射保护剂,可以修复辐射诱导的短暂活性氧。 | |||
T7465 |
4-Methylbenzylidene camphor
Enzacamene,4-甲基苄亚基樟脑,3-(4-甲基苯亚甲基)樟脑,4-MBC |
AChE | Neuroscience |
4-Methylbenzylidene camphor 是有机的樟脑衍生物,应用于化妆品行业,具有保护皮肤抵抗紫外线(特别是紫外线B 辐射)的能力。 | |||
T31929 |
Giripladib
PLA 695,PLA-695,PLA695 |
Phospholipase | Metabolism |
Giripladib (PLA695)(PLX-695)是一种cPLA2特异性抑制剂,可抑制辐射诱导的内皮细胞磷酸化ERK 和磷酸化Akt 的增加。 | |||
T6616 |
Ondansetron hydrochloride
SN 307,盐酸昂丹司琼,帕罗西汀杂质A,Ondansetron HCl,Emeset,GR 38032 HCl,NSC 665799,Zofran |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ondansetron hydrochloride (Zofran) 是5-HT3受体的拮抗剂,可用作化疗后止吐剂。 | |||
T2020 |
RGW 611
|
Others | Others |
RGW 611 是一种能够增强辐射且诱导缺氧 V79-379A 细胞死亡的吗啉衍生物。 | |||
T6970 |
RK33
RK-33,RK 33 |
COX | Immunology/Inflammation; Neuroscience |
RK33 (RK 33) 是 DDX3(一种 RNA 解旋酶)的一流小分子抑制剂,可导致 G1 细胞周期停滞,诱导细胞凋亡,并促进 DDX3 过表达细胞的辐射增敏。 | |||
T1110 |
Meclizine dihydrochloride
Meclozine dihydrochloride,NSC28728,Meclizine 2HCl,盐酸美克洛嗪 |
Apoptosis; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Meclizine dihydrochloride (NSC28728) 是一种组胺 H1 拮抗剂,用于治疗妊娠期间的晕动病、眩晕和恶心以及放射病。它是小鼠组成型雄甾烷受体激动剂,是人 CAR 的反向激动剂。它可透过血脑屏障,可用于多聚谷氨酰胺毒性障碍方面的研究。 | |||
T14133 |
AEOL-10150 pentachloride
|
Others | Others |
AEOL-10150 pentachloride 是一种超氧化物歧化酶模拟物,也是一种金属卟啉催化抗氧剂,可保护肺免受辐射损伤。 | |||
T2386 |
Pirfenidone
S-7701,AMR-69,S-7701,AMR69,吡非尼酮 |
CCR; TGF-beta/Smad | Immunology/Inflammation; Microbiology/Virology; Stem Cells |
Pirfenidone (AMR69) 是一种抗纤维化剂,可减弱纤维细胞中CCL2和CCL12的产生。它可抑制细胞生长,并能降低人胶质瘤细胞系中的TGF-β2蛋白水平,具有抗炎活性。 | |||
T22070 |
DBIBB
|
LPA Receptor | GPCR/G Protein |
DBIBB 是一种特异性溶血磷脂酸 (LPA2) 的 2 型 G 蛋白偶联受体的非脂质激动剂,是一种能够治疗高强度γ 射线对造血和胃肠系统引起的急性放射综合征的潜在活性分子 ,是一种作未有机合成和药物研究中的中间体。 DBIBB 可用于制备各种化合物,可减轻胃肠道辐射综合征,增加肠隐窝存活率和肠细胞增殖,并减少细胞凋亡 。 | |||
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。 | |||
T20681 |
Estramustine
NSC-89201,NSC 89201,LEO 275,LEO275,雌莫司汀,NSC89201,LEO-275 |
Microtubule Associated | Cytoskeletal Signaling |
Estramustine (LEO-275) 是一种与雌二醇相连的氮芥,通常为磷酸盐。它已被用于治疗前列腺肿瘤;还具有防辐射功能。它被前列腺细胞选择性吸收,并通过干扰微管动力学和降低血浆睾酮水平发挥抗肿瘤作用。 | |||
T33701 |
NM-3
NM-3,isocoumarin,NM 3,Isocoumarin NM-3,NM3 |
Apoptosis; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB |
NM-3 是一种可口服的抗血管生成的抑制剂,具有抗肿瘤活性。NM-3在体外和体内可当作辐射调节剂使用。NM-3抑制血管内皮生长因子(VEGF),从而抑制内皮细胞的增殖。NM-3与活性氧的机制诱导细胞凋亡有关。 | |||
T34467 |
S 75
S75,S-75 |
||
S 75 is a compound with radiation protective action. | |||
T13862L |
Recilisib sodium
Brand name: Ex-RAD,ON 01210.Na,ON01210,ON-01210 |
||
Recilisib, also known as ON 01210.Na, is a radioprotectant, which modifys cell cycle distribution patterns in cancer cells subjected to radiation therapy, and it has been identified as a potential candidate for radiation protection studies. It appears tha | |||
T4451L |
Estramustine phosphate
LS 299,NSC 89199,NSC-89199,LS-299,LS299 |
||
Estramustine phosphate can be used to treat prostatic neoplasms; also has radiation protective properties. | |||
T3289L2 |
Amifostine sodium
WR-2721 sodium,WR2721 sodium,WR 2721 sodium |
||
Amifostine sodium is a phosphorothioate proposed as a radiation-protective agent. It causes splenic vasodilation and may block autonomic ganglia. | |||
T31825 |
Fluoromisonidazole
|
||
Fluoromisonidazole, a Radiation-Sensitizing Agent, can be used for imaging tumor hypoxia: imaging the microenvironment for personalized cancer therapy. | |||
T33292 |
Meradine
NSC 22721,NSC-22721,NSC22721 |
||
Meradine can be used for the treatment of radiation injury. | |||
TP2405 |
Romurtide
MDP-lys(L18),CCRIS 1220,DJ-7041,Nopia |
||
Romurtide is a synthetic muramyl dipeptide analog and can be used for the prophylaxis of leukocytopenia during radiation therapy. | |||
T3289L |
Amifostine Hydrate
|
||
Amifostine Hydrate is a radiation protective agent that induces splenic vasodilation and blocks autonomic ganglion. | |||
T33407 |
MitoEbselen-2 chloride
MitoPeroxidase-2,MitoPeroxidase 2,MitoEbselen 2,MitoEbselen-2 |
||
MitoEbselen-2 is a radiation mitigator which reduces lipid hydroperoxides and prevents apoptotic cell death. When administered 24 hours postirradiation, MitoEbselen-2 was shown to increase the survival of mice exposed to whole body γ-irradiation. | |||
T34357 |
Ro 31-0313
Ro 310313,Ro-31-0313 |
||
Ro 31-0313 is a metabolite of Ro 03-8799, radiation sensitizing agent. | |||
T11118 |
Duocarmycin SA
|
Others | Others |
Duocarmycin SA is an extremely potent cytotoxic agent and antitumor antibiotic that induces sequence-selective alkylation of duplex DNA, with an IC50 of 10 pM. It demonstrates synergistic cytotoxicity against glioblastoma multiforme (GBM) cells when combined with proton radiation in vitro. | |||
T82768 |
CBLB 612
|
||
CBLB 612是一种具有双重功效的化合物,既能作为抗辐射辅助剂,也能用作抗肿瘤剂。 | |||
T38267 |
Valeryl-L-carnitine (chloride)
Valeryl-L-carnitine (chloride),L-Valerylcarnitine |
||
Valeryl-L-carnitine is a short-chain acylcarnitine and a derivative of L-carnitine . Valeryl-L-carnitine levels increase in the serum of rhesus monkeys following exposure to 7 and 10 Gray units (Gy) of ionizing radiation.[1] | |||
T72969 |
Actinoquinol
阿克汀喹 |
||
Actinoquinol 是一种 UVB 吸收剂,有助于人眼抵御光氧化和其他氧化。 | |||
T35821 |
CAY10721
|
||
CAY10721 is an inhibitor of sirtuin 3 (SIRT3), a class III HDAC (39% SIRT3 inhibition at 200 μM). Upregulation of SIRT3 transcription is associated with oral squamous cell carcinoma (OSCC) and breast cancer with lymph node involvement, while SIRT3 down-regulation inhibits the growth of OSCC cells and sensitizes them to radiation and chemotherapy. | |||
T36704 |
CCT241533 dihydrochloride
CCT 241533 dihydrochloride |
||
Potent Chk2 inhibitor (IC50 = 3 nM). Shows >63-fold selectivity for Chk1 over Chk2 and a panel of 84 other kinases. Inhibits Chk2 activation in response to etoposide-induced DNA damage in HT29 cells. Blocks ionizing radiation-induced apoptosis of mouse thymocytes. Caldwell et al (2011) Structure-based design of potent and selective 2-(quinazolin-2-yl)phenol inhibitors of checkpoint kinase 2. J.Med.Chem. 54 580 PMID:21186793 | |||
T33487 |
Motexafin gadolinium
PCI0120,Gd texaphyrin,PCI-0120,PCI 0120,Gd-Texgadolinium,API-GP 3 |
||
Motexafin gadolinium, also known as PCI 0120, is a synthetic metallotexaphyrin with radiosensitizing and chemosensitizing properties. Motexafin gadolinium accumulates in tumor cells preferentially due to their increased rates of metabolism, generating rea | |||
T11449 |
Golotimod hydrochloride (229305-39-9 free base)
Golotimod hydrochloride,Gamma-D-glutamyl-L-tryptophan hydrochloride,SCV 07 hydrochloride |
STAT | JAK/STAT signaling; Stem Cells |
Golotimod (SCV 07) hydrochloride 是一种免疫调节肽,具抗菌活性,能显著提升抗结核疾病研究效果。该化合物通过刺激胸腺和脾细胞增殖、改善巨噬细胞功能,展现其生物调节能力。此外,Golotimod hydrochloride 通过抑制STAT3信号传导,有效调节接受放疗或与顺铂联用治疗动物模型中的口腔粘膜炎持续时间和严重程度。还显示出对研究复发性生殖器单纯疱疹病毒 2 型 (HSV-2) 具有潜在应用价值。 | |||
T72009 |
N-Phenylthiourea
|
||
N-Phenylthiourea is a tyrosinase inhibitor and building block. It increases the susceptibility of SK-MEL-188 melanoma cells in melanogenesis-inducing conditions to γ-radiation-induced cytotoxicity when used at a concentration of 0.01 μM. N-Phenylthiourea has been used as a precursor in the synthesis of compounds with antibacterial and antifungal activities. It has also been used as a genetic marker for taste because only some people detect it as a bitter taste. | |||
T81708 |
Nagrestipen
|
||
Nagrestipen 是一种人巨噬细胞炎症蛋白-1α 变体,也称为 ECI 301,主要用于癌症、肿瘤、转移、放射肿瘤学以及肿瘤转移研究试验,具有显著的抗肿瘤活性。 | |||
T71908 |
NU1085
|
||
NU1085 is a potent poly(ADP-ribose) polymerase (PARP) inhibitors have been developed that potentiate the cytotoxicity of ionizing radiation and anticancer drugs. The biological effects of NU1085 [Ki = 6 nM], in combination with temozolomide (TM) or topotecan (TP) have been studied in 12 human tumor cell lines (lung, colon, ovary, and breast cancer). Cells were treated with increasing concentrations of TM or TP +/- NU1085 (10 microM) for 72 h. | |||
T69714 |
Etanidazole
|
||
Etanidazole (SR-2508) is a 2-nitroimidazole drug with radiosensitizing properties. Etanidazole depletes glutathione and inhibits glutathione transferase, thereby enhancing the cytotoxicity of ionizing radiation. This agent may also be useful as an imaging agent for identifying hypoxic, drug-resistant regions of primary tumors or metastases. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus). | |||
T68708 |
Denibulin HCl
|
||
Denibulin (MN-029) is a novel vascular-disrupting agent that reversibly inhibits microtubule assembly, resulting in disruption of the cytoskeleton of tumor vascular endothelial cells. The results of preclinical study demonstrated that MN-029 could cause rapid vascular shutdown in solid tumors, dose-dependent secondary tumor cell killing, and effective enhancement of the antitumor effects of radiation and cisplatin chemotherapy. | |||
T41037 |
Ecamsule disodium
|
||
Ecamsule disodium is a versatile UVA filter compound commonly employed in the formulation of sunscreen products. Its primary role is to mitigate the potential harm posed by solar radiation through the prevention of various biological repercussions induced by UV exposure. These include the inhibition of pyrimidine dimer formation, the reduction of p53 protein accumulation, and the downregulation of collagenase 2 expression. | |||
T78346 |
Superoxide dismutase
SOD |
||
超氧化物歧化酶(SOD)是能清除超氧阴离子的抗氧化酶,它将自由基转化为氧气和过氧化氢,防止过氧亚硝酸盐的形成和进一步损伤。该酶在抗炎、抗肿瘤、辐射防护及抗衰老领域有着广泛应用和研究。 | |||
T63464 | ERCC1-XPF-IN-1 | ||
ERCC1-XPF-IN-1 是有效的、高亲和力的 ERCC1-XPF 抑制剂 (IC50: 0.49 μM)。ERCC1-XPF-IN-1 能够抑制 CPDs 的去除,降低环磷酰胺对结直肠癌细胞的毒性,提高了 UV 辐射的细胞毒性作用,阻碍 DNA 修复。 | |||
T29890 |
AlPcS4
Aluminum phthalocyanine tetrasulfonate tetrasodium,Chloroaluminum tetrasulfophthalocyanine |
||
AlPcS4 , also known as aluminum phthalocyanine tetrasulfonate Chloroaluminum tetrasulfophthalocyanine; or AlS4Pc, AlPcS4(a), is a potent photosensitizer, and is potentially useful in cancer sonodynamic therapy and cancer photodynamic therapy. Aluminum pht |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3399 |
Psoralidin
|
Others; Estrogen/progestogen Receptor; Reactive Oxygen Species; Lipoxygenase; Gamma-secretase; Akt; COX; Antibacterial | Cytoskeletal Signaling; Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB; Others; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Psoralidin 是COX-2和5-LOX 的抑制剂,有抗癌,抗菌和抗炎作用。它显著下调NOTCH1信号传导,还极大地诱导活化氧产生。 | |||
TN1921 |
Meloside A
异牡荆素-2''-O-葡萄糖苷,Isovitexin 2''-O-glucoside,Isovitexin 2''-O-β-D-glucoside |
Others | Others |
Meloside A (Isovitexin 2''-O-β-D-glucoside) 是一种从大麦中提取的苯丙烷类天然产物。 Meloside A 对过量的 UV-B 辐射具有抗氧化和保护作用,并与对病原体的抵抗力有关。 | |||
T2804 |
Panaxatriol
人参三醇,Panaxtriol |
Others | Others |
Panaxatriol (Panaxtriol) 是一种能够减轻由于辐射损伤造成的骨髓抑制的天然产物。 | |||
TMO2685 |
10-Hydroxydecanoic Acid
NSC 15139,10-羟基癸烯酸,10-羟基癸酸 |
Antibacterial | Microbiology/Virology |
10-Hydroxydecanoic Acid (NSC 15139) 是一种存在于蜂王浆中的 10-hydroxy-trans-2-decenoic acid 的饱和脂肪酸,具有抗炎活性。 | |||
T1556 |
Ornidazole
Tiberal,Ornidazolum,NSC 95075,Ro 7-0207,奥硝唑 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Ornidazole (Tiberal) 是一种5-硝基咪唑衍生物,能抗原生动物和厌氧菌。 | |||
T4759 |
Urocanic acid
4-Imidazoleacrylic acid,尿刊酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Urocanic acid (4-Imidazoleacrylic acid), synthesized in the epidermis, functions as a primary absorber of ultraviolet (UV) radiation in mammalian skin. | |||
T3O2784 |
Vitamin B6
维生素B6 |
Others | Others |
Vitamin B6 是人体某些辅酶的成分,参与多种代谢反应,特别是与氨基酸代谢有关。维生素B6在防治妊娠和放射病呕吐中的临床应用。 | |||
T15705 |
Laminaran
β-1,3-Glucan |
||
Laminaran 是一种从褐藻中分离出来的 β-1-3-葡聚糖,常作为 Dectin-1 的典型配体,具有抗癌、免疫调节和辐射防护作用。 Laminaran 可被葡糖酶催化。Laminaran 在体内外实验中显示出抗肿瘤活性,可用于预防和治疗癌症。 | |||
T2A2532 |
L-Histidine
Glyoxaline-5-alanine,L-(-)-Histidine,L-组氨酸,histidine,组氨酸,L-Hisidine |
Mitochondrial Metabolism; Endogenous Metabolite | Metabolism |
L-Histidine (L-(-)-Histidine) 是人类生长和组织修复所需的一种半必需氨基酸(儿童应从食物中获得)。 L-Histidine 是线粒体谷氨酰胺转运的抑制剂。 | |||
T2O2733 |
L-Cystine
Cystine Acid,cystine,胱氨酸,L-胱氨酸 |
Antioxidant; Ferroptosis; Endogenous Metabolite | Apoptosis; Metabolism; oxidation-reduction |
L-Cystine (Cystine Acid) 是一种从半胱氨酸氨基酸硫醇侧链氧化获得的含硫衍生物。它起到抗氧化剂的作用,保护组织免受辐射和污染,减缓衰老过程。它还有助于蛋白质合成。 | |||
T5S0045 |
Isofraxidin
6,8-Dimethoxyumbelliferone,异秦皮啶,Phytodolor,异嗪皮啶 |
MMP; ERK; p38 MAPK; TLR; COX | Immunology/Inflammation; MAPK; Neuroscience; Proteases/Proteasome |
Isofraxidin (Phytodolor) 是来自刺五加的香豆素成分,抑制MMP-7表达和人肝癌细胞侵袭。它作用于肝癌细胞,抑制ERK1/2磷酸化。它减弱iNOS 和COX-2表达,还抑制TLR4/髓样分化蛋白 2 复合物的形成。 | |||
TN1821 |
Kaempferol 3-O-arabinoside
山奈酚-3-O-α-L-吡喃阿拉伯糖苷,堪非醇 3-O-阿拉伯糖苷 |
ROS; Antifection | Immunology/Inflammation; Microbiology/Virology |
Kaempferol-3-O-α±-D-arabinoside displays cytotoxic and high antioxidant activity.Kaempferol-3-O-arabinoside and kaempferol-3-O-glucoside can function as antioxidants in biological systems, particularly skin exposed to UV radiation by scavenging ROS, and protect cellular membrane against ROS; they can be applicable to new cosmeceuticals for antioxidant, antiaging, and antibacterial activity. | |||
T82046 |
Irisquinone
|
||
Irisquinone,一种具有抗癌活性的天然产物,同时作为癌症放射增敏剂。该化合物通过降低GSH水平并抑制DNA单链断裂修复,展现其药理作用。 |