PD-1-IN-1 (CA-170)
(Synonyms: CA-170) 目录号 : GC19225PD-1-IN-1 (CA-170) 是一种具有口服活性的免疫检查点调节蛋白VISTA和PD-L1双重抑制剂。
Cas No.:1673534-76-3
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Cell experiment [1]: | |
Cell lines | Human PBMCs |
Preparation method | Human PBMCs from healthy donors were pre-cultured at high density (1×107 cells/ml) for 48 h to increase cell–cell contacts and immune scanning. The cells were then harvested and treated with anti-CD3 or anti-CD3 + anti-CD28 antibodies as positive controls, and PD-1-IN-1 (CA-170) (10 nM to 1000 nM). Release of IL-2, IFN-γ, and TNF-α was measured in the culture supernatants at 48 h. |
Reaction Conditions | 10-1000 nM ; 48 h |
Applications | In human PBMCs, CA-170 did not induce significant IL-2, IFN-γ, and TNF-α levels in both normal culture conditions or high-density culture conditions, while an antibody against CD28 induced as expected. |
Animal experiment [2]: | |
Animal models | Female A/J mice |
Preparation method | Mice were divided into five groups: (a) control mice that received PBS; (b) adjuvant control mice that received a STING agonist plusAddaVax; (c) KVax mice treated with KVax plus adjuvant; (d) PD-1-IN-1 (CA-170) treatment (10 mg/kg in PBS,) by oral gavage five times per week; (e) combined treatment with KVax/adjuvant plus PD-1-IN-1 (CA-170). Mice were administered one dose of the carcinogen vinyl carbamate31 (VC) by i.p. injection (16 mg/kg in sterile saline). PD-1-IN-1 (CA-170) treatment was started one week after VC induction of lung adenocarcinoma. |
Dosage form | 10 mg/kg; p.o. |
Applications | PD-1-IN-1 (CA-170) treatment decreased tumor load by 63% relative to the adjuvant control group. |
References: |
PD-1-IN-1 (CA-170) is an orally active dual inhibitor of the immune checkpoint regulatory proteins VISTA and PD-L1[1]. PD-1-IN-1 (CA-170) does not directly bind to the target proteins; its mechanism of action might involve blocking their downstream signaling pathways[2]. PD-1-IN-1 (CA-170) exhibits anti-tumor activity similar to that of PD-1 monoclonal antibodies and offers advantages in terms of biosafety[3].
In vitro, PD-1-IN-1 (CA-170) (10-1000nM) treatment of human peripheral blood mononuclear cells (PBMCs) for 48h did not induce the secretion of cytokines IL-2, IFN-γ, and TNF-α, while anti-CD28 antibodies could induce this secretion [4].
In vivo, oral administration of PD-1-IN-1 (CA-170) (10 mg/kg) for 14 days inhibited tumor growth in a mouse model of colon cancer by 36%. However, it did not show significant efficacy in severely immunocompromised mice, demonstrating that the efficacy of PD-1-IN-1 (CA-170) relies on an immune-mediated mechanism[4]. In a mouse model of lung cancer, oral administration of PD-1-IN-1 (CA-170) (10 mg/kg) for 28 days reduced tumor burden by 63%, increased the number of intratumoral CD8+ T cells, and inhibited lung cancer metastasis[5].
References:
[1]Lazorchak A S, Patterson T, Ding Y, et al. Abstract A36: CA-170, an oral small molecule PD-L1 and VISTA immune checkpoint antagonist, promotes T cell immune activation and inhibits tumor growth in pre-clinical models of cancer[J]. Cancer Immunology Research, 2017, 5: A36-A36.
[2]Musielak B, Kocik J, Skalniak L, et al. CA-170–a potent small-molecule PD-L1 inhibitor or not?[J]. Molecules, 2019, 24(15): 2804.
[3]Wu Q, Jiang L, Li S, et al. Small molecule inhibitors targeting the PD-1/PD-L1 signaling pathway[J]. Acta Pharmacologica Sinica, 2021, 42(1): 1-9.
[4]Sasikumar P G, Sudarshan N S, Adurthi S, et al. PD-1 derived CA-170 is an oral immune checkpoint inhibitor that exhibits preclinical anti-tumor efficacy[J]. Communications biology, 2021, 4(1): 699.
[5]Pan J, Chen Y, Zhang Q, et al. Inhibition of lung tumorigenesis by a small molecule CA170 targeting the immune checkpoint protein VISTA[J]. Communications biology, 2021, 4(1): 906.
PD-1-IN-1 (CA-170) 是一种具有口服活性的免疫检查点调节蛋白VISTA和PD-L1双重抑制剂[1]。 PD-1-IN-1 (CA-170) 不与靶点蛋白直接结合,作用机制可能是阻断它们的下游信号通路[2]。PD-1-IN-1 (CA-170) 表现出与PD-1单克隆抗体相似的抗肿瘤活性,且在生物安全性方面更具优势[3]。
在体外,PD-1-IN-1 (CA-170)(10-1000nM)处理人外周血单核细胞(PBMCs)48h,不诱导细胞因子IL-2、IFN-γ和TNF-α的分泌,而抗CD28抗体可以诱导[4]。
在体内,PD-1-IN-1 (CA-170)(10 mg/kg)通过口服治疗结肠癌小鼠14天,对肿瘤生长抑制率为36%,但对严重免疫缺陷的小鼠没有显著疗效,证明了PD-1-IN-1 (CA-170)的功效需要免疫介导机制[4]。PD-1-IN-1 (CA-170)(10 mg/kg)通过口服治疗肺癌小鼠28天,使肿瘤负荷降低了63%,促进了肿瘤内CD8+ T细胞的增加,抑制了肺癌的转移[5]。
Cas No. | 1673534-76-3 | SDF | |
别名 | CA-170 | ||
Canonical SMILES | C[C@@H](O)[C@@H](C(O)=O)NC(N[C@H](C1=NC([C@@H](N)CO)=NO1)CC(N)=O)=O | ||
分子式 | C12H20N6O7 | 分子量 | 360.32 |
溶解度 | DMSO : 28.5 mg/mL (79.10 mM) | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
||
Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 2.7753 mL | 13.8766 mL | 27.7531 mL |
5 mM | 0.5551 mL | 2.7753 mL | 5.5506 mL |
10 mM | 0.2775 mL | 1.3877 mL | 2.7753 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。