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12

抑制剂 & 化合物

8

天然产物

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Cat. No. Product Name Target Signaling Pathways
T22800 Glycoprotein B (485-492)

Others Others
Glycoprotein B is a peptide with the sequence H2N-Ser-Ser-Ile-Glu-Phe-Ala-Arg-Leu-OH, MW= 922.04. glycoprotein B is a viral glycoprotein that is involved in the viral cell entry of Herpes simplex virus. The herpesvirus glycoprotein B is the most highly c
T7657 MOG (35-55) mouse, rat

髓鞘少突胶质细胞糖蛋白,MOG (35-55)

Others Others
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat (MOG (35-55)) 是中枢神经鞘的一个次要成分。它能诱导强效的 T 细胞和 B 细胞反应,同时是高度脑源性的。它能够引发复发缓解性神经系统疾病,伴有广泛的斑块样脱髓鞘。
T6075 Epothilone B

帕妥匹隆,Patupilone,EPO 906

Apoptosis; Microtubule Associated; Antibiotic; Antifungal Apoptosis; Cytoskeletal Signaling; Microbiology/Virology
Epothilone B (EPO 906) 是微管稳定剂,Ki 为0.71 μM。 它与αβ-微管蛋白异二聚体亚基结合,使αβ-微管蛋白解离减少。
TP1534 HSV-gB2 (498-505)

HSV-gB2 498-505

This is the immunodominant epitope gB-8p from herpes simplex virus (HSV) glycoprotein B (gB), amino acids 498 to 505.
T74492 CD22 ligand-1

CD22ligand-1 (compound 12) 是一种有效的选择性CD22配体,对 hCD22 和 MAG 的KD 值分别为 0.335、30.7 µM。CD22ligand-1 具有研究 B 细胞相关疾病的潜力。
T36942 SSAA09E1

SSAA09E1

SSAA09E1 is an inhibitor of severe acute respiratory syndrome coronavirus (SARS-CoV) viral entry.1It reduces infection of HEK293T cells transiently transfected with angiotensin-converting enzyme 2 (ACE2) by an HIV-based virus system pseudotyped with SARS-CoV surface glycoprotein (EC50= 6.7 μM). SSAA09E1 also inhibits the proteolytic activity of cathepsin L (IC50= 5.33 μM) but not cathepsin B when used at a concentration of 20 μM. 1.()
T77010 Fiztasovimab

Fiztasovimab (NPC-21; EV2038) 是一种全人 IgG1λ 单克隆抗体,具有抗人巨细胞病毒 (hCMV) 活性。Fiztasovimab 通过结合 hCMV 包膜上糖蛋白 B 的抗原结构域 1 发挥中和活性。Fiztasovimab 还抑制 hCMV 的细胞间传播。
T77906 Briobacept

BR 3FC

Briobacept (BR 3FC)为专门针对BLyS(BAFF)的单克隆抗体,具有诱导B细胞凋亡(apoptosis)的能力。该化合物是一种重组糖蛋白,由两个BLyS受体(BR3)以及人类IgG1 Fc结构域构成。Briobacept主要用于类风湿关节炎(RA)的研究领域。
T68860 Iso-Fludelone

Iso-Fludelone is the third-generation epothilone B analogue with potential anti-mitotic and antineoplastic activites. Iso-fludelone binds to tubulin and induces microtubule polymerization and stabilizes microtubules against depolymerization, which may result in the inhibition of cell division, the induction of G2/M arrest, and apoptosis. Compared to other generations of epothilones, iso-fludelone exhibits increased stability, water solubility, potency, duration of action, tumor penetration as we...
T80919 Tumour-associated MUC1 epitope

Tumour-associated MUC1 epitope是一种具有标志性的生物活性肽。作为高度糖基化的I型跨膜糖蛋白MUC1的一部分,该肽通过特定的胞外结构域展现,该结构域包含20个氨基酸组成的可变数量串联重复序列(VNTR)。在多种人类腺癌及血液恶性肿瘤(如多发性骨髓瘤和B细胞淋巴瘤)中细胞表面表达过量,因此,MUC1是许多免疫治疗策略的关键靶点。
T81772 MOG (92–106), mouse, rat

MOG (92–106), mouse, rat 是一种来自小鼠/大鼠髓磷脂少突胶质细胞糖蛋白的生物活性肽,包含氨基酸片段92至106。在MOG (92–106) 诱导的实验性自身免疫性脑脊髓炎模型中,小鼠会对次级髓磷脂抗原呈现出广泛的B细胞反应性,尽管T细胞反应较弱。该肽段在SJL小鼠、DA大鼠以及恒河猴中均可诱导严重的脑炎。
T83910 S1PL-IN-31

Sphingosine-1-Phosphate Lyase Inhibitor 31,S1PL Inhibitor 31,S1P Lyase Inhibitor 31

S1PL-IN-31是一种鞘氨醇-1-磷酸(S1P)裂解酶的抑制剂(IC50 = 210 nM),同时也是Smoothened(Smo)受体的对抗剂(IC50 = 440 nM)。在体内,S1PL-IN-31 (每天2 mg/kg)能够防止实验性自身免疫性脑炎(EAE)模型大鼠中,由髓鞘少突胶质细胞糖蛋白(MOG)肽段MOG29-152诱发的颈部及胸部淋巴细胞渗透和神经肌肉虚弱。该化合物降低了大鼠的淋巴细胞总数及CD4+ T细胞、CD8+ T细胞和B细胞的水平。S1PL-IN-31 (每天3及10 mg/kg剂量)在雄性和雌性大鼠心脏和淋巴结中增加了S1P水平,并且在雌性大鼠中降低了心率。

化合物

Glycoprotein B (485-492)
Cat.No: T22800
Synonym:
Target: Others
MOG (35-55) mouse, rat
Cat.No: T7657
Synonym: 髓鞘少突胶质细胞糖蛋白,MOG (35-55)
Target: Others
Epothilone B
Cat.No: T6075
Synonym: 帕妥匹隆,Patupilone,EPO 906
Target: Apoptosis, Microtubule Associated, Antibiotic, Antifungal
HSV-gB2 (498-505)
Cat.No: TP1534
Synonym: HSV-gB2 498-505
Target:
CD22 ligand-1
Cat.No: T74492
Synonym:
Target:
SSAA09E1
Cat.No: T36942
Synonym: SSAA09E1
Target:
Fiztasovimab
Cat.No: T77010
Synonym:
Target:
Briobacept
Cat.No: T77906
Synonym: BR 3FC
Target:
Iso-Fludelone
Cat.No: T68860
Synonym:
Target:
Tumour-associated MUC1 epitope
Cat.No: T80919
Synonym:
Target:
MOG (92–106), mouse, rat
Cat.No: T81772
Synonym:
Target:
S1PL-IN-31
Cat.No: T83910
Synonym: Sphingosine-1-Phosphate Lyase Inhibitor 31,S1PL Inhibitor 31,S1P Lyase Inhibitor 31
Target:
Cat. No. Product Name Target Signaling Pathways
T12540 Pristinamycin IA

Mikamycin IA,普利霉素IA,Mikamycin B

Others; Antibiotic; P-gp Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others
Pristinamycin IA (Mikamycin B) 是 P-糖蛋白的底物,也是一种环肽类大环内酯抗生素。
TJS1159 Chrysosplenetin

猫眼草黄素,Chrysosptertin B

P450; Ferroptosis; P-gp Apoptosis; Membrane transporter/Ion channel; Metabolism; Neuroscience
Chrysosplenetin 是青蒿和其他几种中草药中的一种多甲氧基化黄酮类天然产物,抑制 P-gp 活性并逆转由青蒿素诱导的上调的 P-gp 和 MDR1 水平。
T6S1917 Schisandrol B

Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B

P450; Reactive Oxygen Species; Autophagy Autophagy; Immunology/Inflammation; Metabolism; NF-κB
Schisandrol B (Besigomsin) 是华中五味子的主要活性成分,具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生,也抑制 P-糖蛋白和CYP3A 的活性。
T4085 Paris saponin VII

重楼皂苷 VII,Chonglou Saponin VII,Polyphyllin-VII,Dioscinin,Paris saponin-VII

Apoptosis; BCL; Others; PARP; p38 MAPK; Akt; Caspase; P-gp; Autophagy Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; MAPK; Membrane transporter/Ion channel; Neuroscience; Others; PI3K/Akt/mTOR signaling; Proteases/Proteasome
Paris saponin VII (Dioscini) 是从延龄草的根和根茎中分离的一种甾体皂苷。它减弱线粒体膜电位,增加凋亡相关蛋白的表达,并降低Bcl-2、caspase-9、caspase-3、PARP-1和p-Akt 的蛋白表达水平。它在 K562/ADR 细胞中诱导强烈的自噬,可研究白血病。
TN2256 Taccalonolide B

根薯酮内酯B,根薯酮内酯 B

Microtubule Associated Cytoskeletal Signaling
Taccalonolide B 是从广西裂果薯中分离得到的一种微管稳定剂,具有抗肿瘤活性。它抑制 SK-OV-3 细胞的生长,IC50 为 208 nM,在体外对过表达 P-糖蛋白 (Pgp) 和多药耐药蛋白 (MRP7) 的细胞系有效。
TN5114 Taxinine

P-gp Membrane transporter/Ion channel; Neuroscience
Taxinine and Taxinine B can inhibit the drug transport by P-glycoprotein in multidrug-resistant cells.
TN5113 Taxinine B

Others Others
Taxinine and taxinine B can inhibit the drug transport by P-glycoprotein in multidrug-resistant cells. Taxinine B shows stronger inhibitory effects than acetylsalicylic acid (ASA) on platelet aggregation induced by arachidonic acid (AA).
TN1099 Dihydroevocarpine

MAO; P-gp; Antifection Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience
Dihydroevocarpine shows potent anti-Helicobacter pylori activity with the minimum inhibitory concentration (MIC) value of 10-20 microg/ml. Dihydroevocarpine is a moderate modulator of p-glycoprotein (p-gp) activity; it shows more potent inhibitory effects against MAO-B compared to MAO-A.

天然产物

Pristinamycin IA
Cat.No: T12540
Synonym: Mikamycin IA,普利霉素IA,Mikamycin B
Target: Others, Antibiotic, P-gp
Chrysosplenetin
Cat.No: TJS1159
Synonym: 猫眼草黄素,Chrysosptertin B
Target: P450, Ferroptosis, P-gp
Schisandrol B
Cat.No: T6S1917
Synonym: Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B
Target: P450, Reactive Oxygen Species, Autophagy
Paris saponin VII
Cat.No: T4085
Synonym: 重楼皂苷 VII,Chonglou Saponin VII,Polyphyllin-VII,Dioscinin,Paris saponin-VII
Target: Apoptosis, BCL, Others, PARP, p38 MAPK, Akt, Caspase, P-gp, Autophagy
Taccalonolide B
Cat.No: TN2256
Synonym: 根薯酮内酯B,根薯酮内酯 B
Target: Microtubule Associated
Taxinine
Cat.No: TN5114
Synonym:
Target: P-gp
Taxinine B
Cat.No: TN5113
Synonym:
Target: Others
Dihydroevocarpine
Cat.No: TN1099
Synonym:
Target: MAO, P-gp, Antifection
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