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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39057 |
Rozanolixizumab
UCB7665 |
Others | Others |
Rozanolixizumab(RYSTIGGO)是一种针对人类新生儿 Fc 受体(FcRn)的高亲和力人源化免疫球蛋白 G4 单克隆抗体,用于研究自身免疫和同种免疫疾病中致病性 IgG 。 | |||
T25742 |
Linzagolix choline
|
GNRH Receptor | GPCR/G Protein |
Linzagolix choline 是一种可口服的非肽类的促性腺激素释放激素(GnRH)拮抗剂。可用于研究子宫肌瘤和子宫内膜异位症相关疼痛。 | |||
T5520L |
Cetrorelix diacetate
NS-75A,醋酸西曲瑞克,SB-075 acetate,SB-075 diacetate,Cetrorelix acetate,NS-75A diacetate |
GNRH Receptor | GPCR/G Protein |
Cetrorelix diacetate (NS-75A) 是GnRH 受体的强效拮抗剂(IC50:1.21 nM)。 | |||
T77456 |
Lumiliximab
IDEC-152,ST-152 |
||
Lumiliximab (IDEC-152) 是一种灵长类化的靶向 CD23 猕猴/人嵌合抗体,对 IgE 抗体的产生有抑制作用,用于研究过敏性疾病。 | |||
T76856 |
Andecaliximab
GS-5745 |
MMP; Virus Protease | Microbiology/Virology; Proteases/Proteasome |
Andecaliximab 是一种靶向基质金属蛋白酶 9 (MMP9) 的重组 IgG4 单克隆抗体。Andecaliximab 在特发性肺纤维化小鼠模型中显示出抗纤维化作用。Andecaliximab 可用于研究胃腺癌和特发性肺纤维化 (IPF) 以及登革热病毒。 | |||
TP1469 |
Lixisenatide acetate (320367-13-3 free base)
Lixisenatide acetate |
Glucagon Receptor | GPCR/G Protein |
Lixisenatide acetate 是一种胰高血糖素样肽 1 受体的激动剂,可用于研究 2 型糖尿病。 | |||
T7005 |
Ulixertinib
BVD-523,VRT752271,优立替尼 |
ERK | MAPK |
Ulixertinib (VRT752271) 是一种有效且可逆的 ERK1/ERK2 抑制剂,可抑制 ERK2 和下游蛋白 RSK 的磷酸化,对 ERK2 的IC50值小于 0.3 nM。 | |||
T11174 |
(R)-Elagolix
恶拉戈利,NBI-56418 |
GNRH Receptor | GPCR/G Protein |
(R)-Elagolix (NBI-56418) 是口服具有活性的、选择性高的非肽类促性腺激素释放激素受体短期有效拮抗剂 (KD = 54 pM)。 | |||
T9921 |
Infliximab
|
TNF | Apoptosis |
Infliximab 是一种与 TNF-α特异性结合的嵌合单克隆 IgG1 抗体,可阻止 TNF-α与 TNFR1和 TNFR2 的相互作用,用于治疗克罗恩病和类风湿性关节炎。 | |||
T17301 |
Opigolix
ASP-1707 |
GNRH Receptor | GPCR/G Protein |
Opigolix (ASP-1707)是一种可口服促性腺激素释放激素 (GnRH) 受体拮抗剂,可用于研究子宫内膜异位症相关疼痛、风湿性关节炎和子宫肌瘤。 | |||
T3630 |
Relugolix
RVT-601,瑞卢戈利,TAK-385 |
GNRH Receptor | GPCR/G Protein |
Relugolix (RVT-601) 是口服有活性的非肽性促性腺激素释放激素的拮抗剂。同 TAK-013 相比,它对人和猴子的受体具有高亲和力和强拮抗活性,它们的 IC50值分别为0.33 nM 和0.32 nM。它可用于研究性激素依赖性疾病,如子宫肌瘤、子宫内膜异位症、前列腺癌等。 | |||
T5520 |
Cetrorelix Acetate
醋酸西曲瑞克,Cetrorelix |
GNRH Receptor | GPCR/G Protein |
Cetrorelix Acetate 是一种GnRH 受体的强效拮抗剂(IC50:1.21 nM)。 | |||
T5031 |
Elagolix sodium
NBI-56418 sodium,恶拉戈利钠 |
GNRH Receptor | GPCR/G Protein |
Elagolix sodium (NBI-56418 sodium) 是人GnRH 受体拮抗剂,其IC50=0.25 nM,Ki=3.7 nM。 | |||
T60625 |
Tigulixostat
LC350189 |
Xanthine Oxidase | Metabolism |
Tigulixostat (LC350189) 是一种新型黄嘌呤氧化酶抑制剂(XOI),可降低尿酸生成,可用于研究痛风相关的疾病。 | |||
T3538 |
Sufugolix
TAK-013 |
LHRH | Endocrinology/Hormones |
Sufugolix (TAK-013) 是一种高效的、有口服活性的黄体激素释放激素(LHRH) 受体拮抗剂(IC50:0.1 nM)。 | |||
T7303 |
LIXIVAPTAN
VPA-985,利伐普坦,WAY-VPA 985 |
Vasopressin Receptor | GPCR/G Protein |
Lixivaptan (VPA-985) 是一种具有口服活性的选择性加压素受体 V2 拮抗剂,对人和大鼠的IC50值分别为 1.2 和 2.3 nM。 | |||
T32873 |
Maralixibat Chloride
SHP-625,SHP625,Livmarli,LUM001 chloride,Lopixibat chloride,Lopixibat,SHP625 chloride,SHP 625 |
Potassium Channel | Membrane transporter/Ion channel |
Maralixibat Chloride (LUM001 chloride) 是一种钠依赖性的胆汁酸转运抑制剂,可阻止胆汁酸在肠肝内的再循环 | |||
TP2337 |
Ganirelix Acetate
|
GNRH Receptor | GPCR/G Protein |
Ganirelix Acetate 是一种促性腺激素释放激素 (GnRH) 受体拮抗剂。 | |||
T10988L |
Degarelix acetate(214766-78-6 free base)
|
GNRH Receptor | GPCR/G Protein |
Degarelix acetate(214766-78-6 free base) 是促性腺激素释放激素受体 (GnRHR) 的竞争性可逆拮抗剂。 | |||
T76830 |
Teneliximab
Chi220,Anti-Human CD40 Recombinant Antibody,BMS 224819 |
TNF | Apoptosis |
Teneliximab (Chi220) 是一种嵌合的单克隆抗体,也是一种肿瘤坏死因子受体超家族成员5(CD40)抑制剂,可阻断CD40-CD40L 的相互作用。Teneliximab 通过CD40 和外周B细胞损耗发挥部分激动剂活性,可用于研究器官移植排斥和类风湿关节炎。 | |||
T73698 |
Basiliximab
CHI 621 |
Interleukin | Immunology/Inflammation |
Basiliximab (CHI 621) 是一种嵌合鼠/人 IgG1 单克隆抗白细胞介素 2 受体 (interleukin-2 receptor) 重组抗体。Basiliximab 具有良好的免疫抑制活性,可用于研究肾移植。 | |||
T10217L |
Abarelix
R3827,阿巴瑞克,PPI 149 |
GNRH Receptor | GPCR/G Protein |
Abarelix (PPI 149) 是一种促性腺激素释放激素 (GnRH) 拮抗剂,用于前列腺癌研究。 | |||
T27837 |
Linzagolix
|
GNRH Receptor | GPCR/G Protein |
Linzagolix 是一种口服有活性的非多肽GnRH 拮抗剂。可用于研究子宫肌瘤、子宫腺肌症、子宫内膜异位症。 | |||
T26040 |
Ramorelix
HOE 013,HOE013,HOE-013 |
||
Ramorelix is an antagonist of luteinizing hormone-releasing hormone (LHRH). | |||
T76962 | Vapaliximab | ||
Vapaliximab (2D10) 是一种抗人VAP-1的单克隆抗体。 | |||
T76754 | Otelixizumab | ||
Otelixizumab (ChAglyCD3) 是一种抗人 CD3单克隆抗体,可用于 1 型糖尿病的研究。 | |||
T75999 |
Balixafortide TFA
|
||
Balixafortide TFA (POL6326 TFA) 是一种有效的,选择性的,耐受性好的肽类CXCR4拮抗剂,其IC50小于 10 nM。Balixafortide TFA 对CXCR4的选择性比包括CXCR7在内的许多受体高出 1000 倍。Balixafortide TFA 以 IC50< 10 nM 阻断β-arrestin 募集和钙通量。Balixafortide TFA 还是一种有效的造血干细胞和祖细胞 (HSPC) 动员剂,并具有抗癌作用。 | |||
T73466 |
Pulixin
|
||
Pulixin 阻碍了 FREP1 与恶性疟原虫感染细胞的裂解物的结合,防止传播至蚊子,其中EC50值为11 µM。同时,Pulixin 抑制无性期恶性疟原虫的增殖,EC50值达47 nM。 | |||
T81925 |
Lixudebart
|
||
Lixudebart为人源化IgG1-kappa亚型抗CLDN1单克隆抗体。 | |||
T81357 |
PTBP1 α3-helix derived peptide P1 TFA
|
||
PTBP1 α3-螺旋衍生的多肽P1是一种多肽,具有抑制RNA结合的能力。 | |||
TP2141 |
Balixafortide TFA (1051366-32-5 free base)
Balixafortide TFA,POL6326 TFA |
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
Balixafortide TFA (POL6326 TFA) is a selective, well-tolerated peptidic CXCR4 antagonist (IC50 < 10 nM). It shows 1000-fold selective for CXCR4 than a large panel of receptors including CXCR7. Balixafortide TFA blocks β-arrestin recruitment and calcium fl | |||
T77049 | Keliximab | ||
Keliximab (SB-210396) 是一种嵌合的人/猕猴IgG1抗CD4单克隆抗体,对可溶性CD4的Kd 值为 1.0 nM。Keliximab 阻断 T 细胞增殖并抑制IL-2的产生。Keliximab 可用于癌症研究。 | |||
T69492 |
Ozarelix
|
||
Ozarelix is a fourth generation GnRH antagonist, induces apoptosis in hormone refractory androgen receptor negative prostate cancer cells modulating expression and activity of death receptors. Mechanistically, LHRH antagonists exert rapid inhibition of luteinizing hormone and follicle stimulating hormone with an accompanying rapid decrease in sex hormones and would therefore be expected to be effective in a variety of hormonally dependent disease states including ovarian cancer, prostate cancer,... | |||
T82708 |
Clenoliximab
IDEC-151 |
||
Clenoliximab (IDEC-151)为一种猕猴-人嵌合型单克隆抗体(immunoglobulin G4),特异性结合于T淋巴细胞表面CD4分子。该化合物主要用于类风湿性关节炎的科研领域。 | |||
T71126 |
Allixin
|
||
Allixin is a phytoallexin found in garlic (Allium sativum) bulbs. Allixin has weak antimicrobial activity and exerts an anti-promoting activity against skin tumors induced by the chemical 12-O-tetradecanoylphorbol-13-acetate (TPA). Allixin also demonstrates an inhibitory effect on aflatoxin B1-induced mutagenesis. | |||
TP2141L |
Balixafortide
POL6326 |
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
Balixafortide (POL6326) is a potent, selective, well-tolerated peptidic CXCR4 antagonist with an IC50 < 10 nM and it is also a potent hematopoietic stem and progenitor cell (HSPC) mobilizing agent. Anti-cancer effects[1][2]. Balixafortide blocks β-arresti | |||
T7005L |
Ulixertinib hydrochloride
Ulixertinib HCl,BVD-523,VRT752271,BVD 523,BVD523,VRT 752271 |
||
Ulixertinib is an inhibitor of ERK protein kinase. Downmodulation of ERK protein kinase activity inhibits VEGF secretion by human myeloma cells and myeloma-induced angiogenesis. Upon oral administration, BVD-523 inhibits both ERK 1 and 2, thereby preventi | |||
T20857 |
Polixetonium chloride
|
||
Polixetonium chloride is a cooling tower biocide. | |||
T70309 |
Dicetrorelix pamoate
|
||
Dicetrorelix pamoate is a synthetic decapeptide with gonadotropin-releasing hormone (GnRH) antagonistic activity. GnRH induces the production and release of luteinizing hormone (LH) and follicle stimulating hormone (FSH) from the gonadotrophic cells of the anterior pituitary. Due to a positive estradiol (E2) feedback at midcycle, GnRH liberation is enhanced resulting in an LH-surge. This LH-surge induces the ovulation of the dominant follicle, resumption of oocyte meiosis and subsequently lutein... | |||
T73327 | Merigolix | ||
Merigolix 是一种有效的促性腺激素释放激素GnRH 拮抗剂。 | |||
T76809 | Galiximab | ||
Galiximab (IDEC 114),一种IgG1类免疫球蛋白单克隆抗体,针对CD80抗原。其可变区来源于灵长类动物,而恒定区则来自人类。Galiximab主要用于研究B细胞淋巴瘤。 | |||
T17236 |
Volixibat
SHP626,LUM002 |
Others | Others |
Volixibat is a highly selective and competitive apical sodium-dependent bile acid transporter inhibitor. Volixibat has the potential for treatment for non-alcoholic steatohepatitis. | |||
T71592 |
Detirelix acetate
|
||
Detirelix acetate is an LHRH Antagonist | |||
T68701 |
Abarelix acetate
|
||
Abarelix acetate is a synthetic third generation gonadotropin-releasing hormone receptor (GnRHR) antagonist. It increases histamine release from rat peritoneal mast cells in vitro and from a human skin model ex vivo. In vivo, abarelix decreases plasma luteinizing hormone (LH) levels six hours post-treatment in castrated rats, with levels returning to baseline within 24 hours.3 Abarelix (2 mg/kg) also transiently decreases plasma testosterone levels in intact rats, with levels returning to baseli... | |||
TP1057 |
Phe-Met-Arg-Phe Like Peptide, Snail Helix aspersa
Phe-Met-Arg-Phe Like Peptide |
||
Phe-Met-Arg-Phe-like peptide, derived from the visceral and somatic muscles of the snail Helix aspersa, is a neuropeptide known as FMRF (Phe-Met-Arg-Phe). This peptide comprises four amino acid residues[1]. | |||
T75991 |
Ganirelix
|
||
Ganirelix为一种竞争性且选择性的促性腺激素释放激素(GnRH)拮抗剂,其主要作用机制为抑制内源性GnRH,从而抑制黄体生成素(LH)及促卵泡激素的释放。 | |||
T28954 |
Teverelix
|
||
Teverelix is a water-soluble antagonist of luteinizing hormone-releasing hormone (LHRH). | |||
T68420 |
Detirelix
|
||
Detirelix is an LHRH antagonist. | |||
T80547 |
Thioether-cyclized helix B peptide, CHBP TFA
|
mTOR | PI3K/Akt/mTOR signaling |
Thioether-cyclized helix B peptide, CHBP(TFA)为Thioether-cyclized helix B peptide, CHBP的三氟乙酸盐形式,通过抑制mTORC1及激活mTORC2来诱导自噬(autophagy),进而增强代谢稳定性及肾脏保护效果。 | |||
T78294 |
Tavolixizumab
MEDI 0562,Tavolimab |
||
Tavolixizumab (MEDI 0562; Tavolimab)为一种针对TNFRSF4(TNF受体超家族成员4)的人源化单克隆抗体,主要应用于癌症免疫学领域的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2985 |
Gypenoside XLIX
绞股蓝皂苷 XLIX,绞股蓝皂苷XLIX |
PPAR | DNA Damage/DNA Repair; Metabolism |
Gypenoside XLIX 是一种达玛烷型糖苷,是绞股蓝的主要成分。它是选择性过氧化物酶体增殖物激活受体 (PPAR)-α激活剂,可抑制细胞因子诱导的血管细胞粘附分子-1 (VCAM-1) 在人体内皮细胞中过度活跃和表达。 | |||
TN4740 |
Parvifolixanthone B
|
Others | Others |
Parvifolixanthone B is a natural product from Garcinia parvifolia. | |||
TN4739 |
Parvifolixanthone A
|
Others | Others |
Parvifolixanthone A is a natural product from Garcinia parvifolia. | |||
TN1066 |
Filixic acid ABA
|
Influenza Virus | Microbiology/Virology |
Filixic acid ABA exhibits inhibitory effects on neuraminidase of influenza virus H5N1 with IC50 as 29.57 ± 2.48 μM, it may have anti-influenza virus activity. | |||
TN6532 |
Polygalasaponin XLIX
|
||
Polygalasaponin XLIX 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6532,CAS号为 1033593-12-2。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04790 |
CXCL5 Protein, Mouse, Recombinant (His)
AMCF-II,GCP-2,Scyb6,LIX,chemokine (C-X-C motif) lig... |
Mouse | P. pastoris (Yeast) |
CXCL5 Protein, Mouse, Recombinant (His) is expressed in yeast with His tag. The predicted molecular weight is 9.4 kDa and the accession number is P50228. |