52
7
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T82221 |
Head activator neuropeptide
|
||
Head activator neuropeptide 是一种源自哺乳动物细胞系的神经元或神经内分泌的有丝分裂原,其通过与GPR37结合来进行信号传递并促进细胞分裂。 | |||
T7459 |
Abametapir
5 5'-二甲基-2,2-联吡啶,HA-44,BRN 0123183 |
MMP; Others; Parasite | Microbiology/Virology; Others; Proteases/Proteasome |
Abametapir (BRN 0123183) 是一种金属蛋白酶抑制剂,能够靶向对卵孵化和虱子发育至关重要的金属蛋白酶。 | |||
T26889 |
Borofalan(10B)
L-4-Boronophenylalanine,4-10硼酸-L-苯丙氨酸 |
Others | Others |
Borofalan(10B) (L-4-Boronophenylalanine) 具有抗肿瘤作用,可用于研究复发性或局部晚期头颈癌。 | |||
TP1114L |
Leucokinin VIII acetate
Leucokinin 8 |
Others | Others |
Leucokinin VIII acetate (Leucokinin 8) 是一种从蟑螂头部提取物中分离的利尿八肽。 | |||
T25284 |
DAC-2-25
DAC 225,DAC-225,DAC 2 25 |
Others | Others |
DAC-2-25是 Hydra 头部再生调节剂。它通过诱导 Hydra 的同源转化而起作用。 | |||
T5330 |
Fluralaner
AH252723,氟雷拉纳,A1443 |
GABA Receptor; Parasite | Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Fluralaner (A1443) 是一种异恶唑啉杀外寄生虫剂。 它有效且选择性地抑制 GABA 受体通道阻滞剂 EBOB 与家蝇头膜的结合,IC50值为 455 pM。 | |||
T17035 |
Temoporfin
替莫卟吩,替莫泊芬 |
Others | Others |
Temoporfin 能够用于头颈部鳞状细胞癌的光动力学研究。 | |||
T0790 |
Carbaryl
1-naphthyl methylcarbamate,甲萘威,Sevin |
AChR | Neuroscience |
Carbaryl (1-naphthyl methylcarbamate) 可作为一种杀虫剂。 | |||
T10337 |
Antimicrobial Compound 1
|
Antibacterial | Microbiology/Virology |
Antimicrobial Compound 1 是一种烷基吡啶鎓化合物,尾部为 12C,头部为 4-羧基。 Antimicrobial Compound 1 对枯草芽孢杆菌和大肠杆菌具有抗菌活性。 | |||
T76696 |
Onvatilimab
JNJ-61610588 |
Others | Others |
Onvatilimab (JNJ-61610588) 是一种人 IgG1κ 抗 VISTA (T 细胞激活的 V 域 Ig 抑制剂) 单克隆抗体。Onvatilimab 具有抗肿瘤活性,可用于治疗晚期头颈癌。 。 | |||
T2618 |
LGK974
LGK 974,LGK-974,NVP-LGK974,WNT974 |
Porcupine | Stem Cells |
LGK974 (NVP-LGK974) 是一种有效的、特异性的、具有口服活性的Porcupine(PORCN) 抑制剂(IC50:0.1 nM)。 | |||
T77423 |
Lirilumab
ONO-4483,IPH2102 |
Virus Protease | Microbiology/Virology |
Lirilumab (IPH2102) 是一种针对杀伤性免疫球蛋白样受体抗体 KIR2D 的抗体,具有抗肿瘤活性,通过 Vav1 依赖性 NF-κB 去抑制增强自然杀伤细胞的抗 HPV+ 宫颈癌活性,可用于研究白血病、头颈部鳞状细胞癌 (SCCHN)。 | |||
T76890 |
Petosemtamab
MCLA 158 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Petosemtamab (MCLA 158) 是一种高效的抗 EGFR (Kd: 0.22 nM) 和抗 LGR5 (Kd: 0.86 nM) 单克隆抗体。Petosemtamab 促使 LGR5+ 癌细胞中的 EGFR 信号传导中断和受体分解。Petosemtamab 可用于头颈部鳞状细胞癌 (HNSCC)、转移性结直肠癌 (CRC) 等实体瘤的研究。 | |||
T71912 |
PD 173955-Analog1
|
||
PD 173955-Analog1 is a potent c-Src inhibitor known to have activity against a variety of cancers including colon, lung, head and neck carcinoma. | |||
T25683 |
Leucomyosuppressin
p-Glu-asp-val-asp-his-val-phe-leu-arg-phe-NH2 |
||
Leucomyosuppressin, isolated from head extracts of the cockroach Leucophaea maderae, inhibits evoked transmitter release at the mealworm neuromuscular junction. | |||
T29965 |
Amethopterin
DL-Amethopterin |
||
Amethopterin is a chemotherapy drug and immune system inhibitor used to treat cancers of the blood, bone, lung, breast, head, and neck. In addition, it can treat rheumatoid arthritis and psoriasis. | |||
TP1114 |
Leucokinin VIII
Leucokinin 8 |
||
Leucokinin VIII is an diuretic octapeptide isolated form head extracts of the cockroach. | |||
T20688 | Leucokinin I | ||
Leucokinin I is an eight amino acid neuropeptide. It is found in the nervous system of the bowfly and isolated from the head of Madeira cockroach Leucophaea maderae. | |||
T21119 |
Cevimeline
AF-102B,西维美林,FKS 508,SNI 2011,HSDB 7286 |
||
Cevimeline, a parasympathomimetic and muscarinic agonist, affects M1 and M3 receptors. Cevimeline has been shown to treat dry mouth and Sj gren's syndrome. It is also used to reduce Xerostomia symptoms and increase salivary flow in head and neck cancer survivors after radiotherapy. | |||
T74742 |
TRPV1 activator-2
|
||
TRPV1 activator-2 (compound 9)为辣椒素类似物,特异性与脂-水通道残基相互作用。 | |||
T69857 |
DB293
|
||
DB293 is an inhibitor of PIT-1 and BRN-3 transcription factors. DB293 binds as head-to-tail stacked dimers in the minor groove of 5'-ATGA sequence, thereby leading to an increase in the size of minor groove. | |||
T19377 | Ioxilan | Others | Others |
Ioxilan is a low-osmolar, nonionic, and tri-iodinated diagnostic contrast agent used for excretory urography and contrast-enhanced computed tomographic (CECT) imaging of the head and body. Intravascularly injected causes opacification of vessels, allowing for radiographic visualization of internal structures until significant hemodilution occurs. | |||
T79506 |
Topoisomerase II inhibitor 15
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseII inhibitor 15 (compound 2g) 为 TopoisomeraseII 的一种抑制剂,能有效诱导细胞凋亡 (apoptotic) 并对头颈部肿瘤展示出较高选择性。 | |||
T76918 | Barecetamab | ||
Barecetamab (ISU-104) 是一种人源话抗 ErbB3单克隆抗体。Barecetamab 可用于复发/转移性 (R/M) 头颈部鳞状细胞癌 (HNSCC) 的研究。 | |||
T28494 |
R-82913
NSC 637653, 9-Cl-Tibo,R 82913,R82913. 9-Cmbib |
||
R-82913 is a RNA-directed DNA polymerase inhibitor. R 82913 reduce 5-HT2 receptor-mediated DOI-head-shakes in mice. R82913 inhibited the replication of thirteen different strains of HIV-1 in CEM cells with a median IC50 of 0.15 microM. R82913 was 20-fold | |||
T77268 |
C13-112-tetra-tail
|
||
C13-112-tetra-tail 是一种阳离子类脂化合物,可用于配制脂质纳米颗粒。 | |||
T74288 |
SQDG
|
||
SQDG 是一种膜脂,头部基团含有糖部分,用于研究结构脂在LNP制剂中的作用。 | |||
T77266 |
C13-112-tri-tail
|
||
C13-112-tri-tail 是一种阳离子类脂化合物,可用于配制脂质纳米颗粒。 | |||
T77267 |
C13-113-tri-tail
|
||
C13-113-tri tail 是一种阳离子类脂化合物,可用于配制脂质纳米颗粒。 | |||
T77269 |
C13-113-tetra-tail
|
||
C13-113-tetra-tail 是一种阳离子类脂化合物,可用于配制脂质纳米颗粒。 | |||
T82188 |
HN-1
|
||
HN-1为一种12-mer多肽,在头颈部鳞状细胞癌(HNSCC)细胞上展现特异性活性。作为肿瘤特异性肽,HN-1可渗透肿瘤组织,并在细胞膜上转移活性分子。 | |||
T83423 |
1-Palmitoyl-2-[3-(diphenylhexatriene)propanoyl]-sn-phosphatidylcholine
|
||
1-Palmitoyl-2-[3-(diphenylhexatriene)propanoyl]-sn-phosphatidylcholine 是一种荧光探针,其极性磷脂酰乙醇胺头基适用于测定脂蛋白与血浆表面脂质的氧化。 | |||
T35907 |
Paraherquamide A
|
||
Paraherquamide A is a mycotoxin anthelmintic originally isolated from P. paraherquei. It binds to acetylcholine receptors (IC50 = 0.5 nM for head homogenates of M. domestica) and acts as an antagonist. Paraherquamide A is toxic to C. elegans (LD50 = 2.5 μg/ml) and effective against T. colubriformis infection in gerbils when used at doses ranging from 0.39 to 200 mg/kg. It is toxic to mice (LD50 = 14.9 mg/kg). | |||
T21964 |
KP372-1
|
||
KP372-1是一种 Akt 的抑制剂,通过阻断 PI3K 通路信号,抑制细胞增殖,同时诱导癌细胞凋亡,可用于头颈部鳞状细胞癌的研究。 | |||
T62790 |
JH-XIV-68-3
|
||
JH-XIV-68-3 是一种选择性的 DYRK1A/B 大环抑制剂。JH-XIV-68-3 在生化和细胞测定中能够选择性作用于 DYRK1A 和近亲 DYRK1B。JH-XIV-68-3 在头颈部鳞状细胞癌 (HNSCC) 细胞系中具有抗肿瘤作用。 | |||
T76372 |
TRAF6 peptide
|
||
TRAF6 peptide 是一种特异性的TRAF6-p62相互作用抑制剂。TRAF6 peptide 能消除 NGF 依赖性TrkA 泛素化。TRAF6 peptide 在诸如阿尔茨海默症 (AD)、帕金森、ALS、头部外伤、癫痫和中风等神经系统性疾病中具有较好的研究潜力。 | |||
T68297 | Dilmapimod tosylate | ||
Dilmapimod tosylate is a potent p38 mitogen-activated protein kinase (MAPK) inhibitor. It was investigated for its anti-inflammatory effect in non-head injury trauma patients at risk for developing acute respiratory distress syndrome. IL-1β was identified as a gene regulated by dilmapimod that could influence c-reactive protein levels. Dilmapimod had been in phase III clinical trials by GlaxoSmithKline for the treatment of rheumatoid arthritis, neuropathic pain, coronary artery disease (CAD) and... | |||
T68661 |
Edatrexate
CGP 30694 |
||
Edatrexate (CGP 30694),即 10-乙基-10-去甲氨基蝶呤,是甲氨蝶呤Methotrexate 的类似物,对耐 MTX 肿瘤具有抗肿瘤活性。Edatrexate 是一种抗叶酸抗代谢物,可用于研究非小细胞肺癌,乳腺癌,非霍奇金淋巴瘤和头颈部癌症的研究。 | |||
T78221 |
TRAF6 peptide TFA
|
E1/E2/E3 Enzyme | Ubiquitination |
TRAF6 peptide TFA是一种抑制TRAF6-p62相互作用的特异性分子,可抑制NGF依赖的TrkA泛素化,展现在阿尔茨海默症(AD)、帕金森病、ALS、创伤性脑损伤、癫痫和中风等神经系统疾病研究中的应用潜力。 | |||
T36368 |
2H-Cho-Arg (trifluoroacetate salt)
|
||
2H-Cho-Arg is a steroid-based cationic lipid that contains a 2H-cholesterol skeleton coupled to an L-arginine head group and can be used to facilitate gene transfection. It forms a complex with plasmid DNA (pDNA) and decreases pDNA migration in an electrophoretic mobility shift assay at +/- charge ratios of 4 or higher. 2H-Cho-Arg facilitates transfection of a luciferase gene into H1299 cells, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and t... | |||
T71491 | Enadoline (Free Base) | ||
Enadoline (Free Base) is a kappa-opioid receptor agonist; PD 129290 (CAM 570; CI 977) is the S,S(-)-enantiomer; PD 129289 (CAM 569) is the corresponding R,R(+)-enantiomer. In human studies, it produced visual distortions and feelings of dissociation, reminiscent of the effects of salvinorin A. It was studied as a potential analgesic, but abandoned because of the dose-limiting effects of dysphoria, which could be expected from a κ-opioid agonist. There was mention of its potential in treating com... | |||
T71211 |
Rizatriptan-d6 benzoate salt
|
||
Rizatriptan-d6 is intended for use as an internal standard for the quantification of rizatriptan by GC- or LC-MS. Rizatriptan is an agonist of the serotonin receptor subtypes 5-HT1B and 5-HT1D. It is selective for 5-HT1B and 5-HT1D receptors over 5-HT1A receptors. Rizatriptan induces vasoconstriction in isolated human middle meningeal arteries. In vivo, rizatriptan reduces head grooming, the number of oculotemporal strokes, eye blinking, and one-eye closures in a Cacna1a mutant transgenic mou... | |||
T37217 |
N-Decanoyl p-Nitroaniline
|
||
N-Decanoyl p-nitroaniline (DepNA) is one of several nitroaniline fatty acid amides which can be used to measure fatty acid amide hydrolase (FAAH) activity. FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its endogenous substrate anandamide (AEA). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. Exposure of DepNA to FAAH activity results in the release of the yellow colori... | |||
T74566 | Phospholipid-PEG-Biotin (MW 5000) | ||
Phospholipid-PEG-Biotin (MW 5000)为含有磷脂的PEG衍生物,适用于脂质体和细胞表面的修饰,及胰岛细胞移植。Phospholipid具亲水性“头部”与疏水性“尾部”结构,PEG为亲水性低毒聚合物,生物素则作为酶辅因子,用于蛋白质标记。 | |||
T35810 |
C24 dihydro Ceramide (d18:0/24:0)
Cer(d18:0/24:0) |
||
C24 dihydro Ceramide is a sphingolipid that has been found in the stratum corneum of human skin.[1] It is found in higher concentrations in female sebum compared to male sebum.[2] C24 dihydro Ceramide levels positively correlate with cytotoxicity in CCRF-CEM, MOLT-4, COG-LL-317h, and COG-LL-332h T cell acute lymphoblastic leukemia (ALL) cell lines.[4] Levels of C24 dihydro ceramide are increased by 149.49-fold in dihydroceramide desaturase 1 (DEGS1) knockdown UM-SCC-22A human head and neck squam... | |||
T36350 |
Cho-Arg (trifluoroacetate salt)
|
||
Cho-Arg is a steroid-based cationic lipid that contains a cholesterol skeleton coupled to an L-arginine head group. It forms a complex with plasmid DNA and decreases plasmid DNA migration in an agarose-gel retardant assay at charge ratios greater than or equal to 4. Cho-Arg facilitates transfection of plasmid DNA into H1299 and HeLa cells in the presence or absence of fetal bovine serum, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and the cav... | |||
T72776 |
NR2F1 agonist 1
|
||
NR2F1 agonist 1 是一种核受体 NR2F1激动剂,可特异性激活恶性细胞的休眠程序。NR2F1 agonist 1 上调 NR2F1 和调节休眠的下游靶基因。NR2F1 agonist 1 通过 NR2F1 激活在头颈部鳞状细胞癌 (HNSCC) 中诱导神经嵴样生长抑制。NR2F1 agonist 1 在小鼠原发肿瘤模型中抑制肿瘤生长。 | |||
T74564 | Phospholipid-PEG-Biotin (MW 2000) | ||
Phospholipid-PEG-Biotin (MW 2000) 是一种PROTAClinker,属于 PEG 类。可用于合成PROTAC 分子。Phospholipid 是一类含有亲水“头”和疏水“尾”的脂类;PEG 是一种低毒性的亲水水溶性聚合物;生物素是一种酶辅因子,可用于标记蛋白质。 | |||
T63556 | EGFR-IN-59 | ||
EGFR-IN-59 是 EGFR 抑制剂,其IC50值为190 nM,也是一直凋亡 (apoptosis) 诱导剂。EGFR-IN-59 对非小肺癌细胞系 (A549) 和正常肺成纤维细胞 (WI38) 表现出细胞毒性的IC50分别为 8.62 和 52.6 μM。EGFR-IN-59 能够用于研究非小细胞肺癌 (NSCLC)、头颈癌、乳腺癌和结直肠癌等多种癌症。 | |||
T36359 |
Dios-Arg (trifluoroacetate salt)
|
||
Dios-Arg is a steroid-based cationic lipid that contains a diosgenin skeleton coupled to an L-arginine head group. It forms a complex with plasmid DNA and decreases plasmid DNA migration in an agarose-gel retardant assay at charge ratio greater than or equal to 4. Dios-Arg facilitates transfection of plasmid DNA into H1299 and HeLa cells in the presence and absence of fetal bovine serum, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and the cav... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7727 |
Se-Methylselenocysteine
Se MSC,SeMCys,MSeC,L-硒甲基硒代半胱氨酸,Se-MSC,SeMSC |
BCL; IAP; Caspase | Apoptosis; Proteases/Proteasome |
Se-Methylselenocysteine (Se-MSC) 是具有口服活性的甲基硒前体,具有强大的抗氧化活性和抗癌活性。Se-Methylselenocysteine 可诱导细胞凋亡。 | |||
T3674 |
Hydroxysafflor yellow A
藏红花,羟基红花黄色素A,HSYA,Safflomin A |
TGF-beta/Smad | Stem Cells |
Hydroxysafflor yellow A (Safflomin A) 是一种黄酮类天然产物,从中药红花中分离得到,具有抗癌作用。 | |||
TN2539 |
1beta-Hydroxyalantolactone
|
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
1beta-Hydroxyalantolactone 是从药用植物大英花的花头中分离出的小分子化合物,可抑制细胞中TNF-α、IL-17、IFN-γ的表达,促进TNF-α、IFN-γ、IL-17的分泌,可防治类风湿性关节炎。 | |||
T3229 |
Cytochalasin D
|
ATPase; p38 MAPK; Calcium Channel; Akt; PI3K | Cytoskeletal Signaling; MAPK; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling |
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertilization processes such as sperm penetration or sperm head decondensation. Cytochalasin D inhibit | |||
T0729 |
Benzyl benzoate
Ascabiol,Novoscabin,Scabitox,苯甲酸苄酯,Benzoic acid benzyl ester |
Parasite | Microbiology/Virology |
Benzyl benzoate (Benzoic acid benzyl ester) 是化妆品中的香料成分,可研究疥疮和蠕形螨相关的炎症性皮肤病。 | |||
T4889 |
2,6-Diaminoheptanedioic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
2,6-Diaminoheptanedioic acid 是内源性代谢产物的一种。 | |||
TN7240 |
Erinacine A
|
ROS | Immunology/Inflammation |
Erinacine A 是一种可从猴头菇中提取出的抗癌化合物,能够通过活性氧类 (ROS) 的产生促使癌细胞死亡。Erinacine A 可能通过参与信号通路的调节从而发挥其抗癌活性。Erinacine A 具有抗癌、抗肿瘤和神经保护活性。 |