货号:A700949
同义名:
Ro 13-7410; Arotinoid acid
TTNPB (Arotinoid Acid)是一种有效的 RAR 激动剂,能够作用于 RARα(IC50 = 5.1 nM)、RARβ(IC50 = 4.5 nM)和 RARγ(IC50 = 9.3 nM),用于研究视黄酸受体的激活。TTNPB与CHIR99021或激活素A结合,分别诱导人或小鼠多能干细胞形成中间中胚层,促进培养的鸡尾神经板外植体的神经元分化。
There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
Inaccessible (Haz class 6.1), Domestic | USD 80+ |
Inaccessible (Haz class 6.1), International | USD 150+ |
Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
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描述 | TTNPB (Ro 13-7410) (GMP) refers to TTNPB produced following GMP guidelines. GMP small molecules serve as appropriate auxiliary reagents for cell therapy manufacture. TTNPB is a highly potent retinoic acid receptor (RAR) agonist. |
体外研究 | TTNPB inhibits binding of [3H]tRA with IC50s of 3.8 nM, 4 nM, and 4.5 nM for human RARα, β, and γ, respectively. TTNPB competes for [3H]tRA binding to CRABPI with IC50s of 1800 nM[1]. The combination of TTNPB (Ro 13-7410) (GMP) (100 nM) and Laduviglusib can induce chondrogenic markers in hiPSCs and form hyaline cartilaginous tissues in vivo[2]. |
Concentration | Treated Time | Description | References | |
H1 hESCs | 3 nM | 4 days | Induce differentiation of H1 hESCs into pancreatic endoderm | Nucleic Acids Res. 2018 Apr 6;46(6):2883-2900. |
human pluripotent stem cells | 6 µM | Used in mesoderm differentiation experiments, TTNPB was added to the medium to promote mesodermal cell differentiation. | Cells. 2025 Jan 24;14(3):184. | |
mouse primary brown adipocytes | 100 nM | 18 h | Pretreatment with TTNPB restored mitochondrial respiration in Rdh1-null brown adipocytes to WT levels and restored the expression of lipolysis-related genes to WT levels. | Cell Mol Life Sci. 2019 Jun;76(12):2425-2447. |
Bovine ear fibroblasts | 1 μM | 6 days | Induce the transdifferentiation of bovine ear fibroblasts into adipocyte-like cells, with a large number of lipid droplets observed on day 6 | Front Cell Dev Biol. 2023 Feb 2;11:1020965. |
M14(5–16) cells | 1 μM | 6 days | To evaluate the effect of TTNPB on the proliferation of M14(5–16) cells, results showed that TTNPB alone reduced cell proliferation by 22%, and in combination with LGD1069, it had an additive effect, reducing cell proliferation by 38%. | Mol Cancer. 2009 Mar 6;8:16. |
L929 mouse fibroblast cell line | 1 µM | 8 days | Induced L929 cells to transform into dermal-papilla-cell-like cells (DPC-LCs), confirmed by alkaline phosphatase (ALP) staining and molecular markers | Int J Mol Sci. 2022 Apr 11;23(8):4213. |
Primary adult mouse fibroblasts | 1 µM | 8 days | TTNPB significantly increased ALP activity in primary adult mouse fibroblasts and confirmed their transformation into DPC-LCs through molecular markers | Int J Mol Sci. 2022 Apr 11;23(8):4213. |
Human embryonic stem cells (H9) | 0.5 μM | 4 days | TTNPB significantly improved the clonal colony formation efficiency of human embryonic stem cells, increasing it from 0-0.3% to 2-3% when used alone, and to 15-17% when combined with Y-27632. | Commun Biol. 2024 Feb 16;7(1):190. |
Human induced pluripotent stem cells (4YF) | 0.5 μM | 4 days | TTNPB significantly improved the clonal colony formation efficiency of human induced pluripotent stem cells, increasing it from 0-0.3% to 2-3% when used alone, and to 15-17% when combined with Y-27632. | Commun Biol. 2024 Feb 16;7(1):190. |
Administration | Dosage | Frequency | Description | References | ||
Nude mice | Full-thickness wound model in nude mice | Subcutaneous injection | 1 µM | Single injection, lasting 3 weeks | Assessed the ability of TTNPB-treated fibroblasts to induce hair follicle regeneration in vivo, results showed TTNPB-treated cells could induce HF-like structure formation | Int J Mol Sci. 2022 Apr 11;23(8):4213. |
Dose | Mice: 0.01 mg/kg - 0.8 mg/kg[3] (p.o.); 1 mg/kg, 10 mg/kg[4] (i.p.) |
Administration | p.o., i.p. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.87mL 0.57mL 0.29mL |
14.35mL 2.87mL 1.43mL |
28.70mL 5.74mL 2.87mL |
CAS号 | 71441-28-6 |
分子式 | C24H28O2 |
分子量 | 348.48 |
SMILES Code | O=C(O)C1=CC=C(/C=C(C2=CC=C3C(C)(C)CCC(C)(C)C3=C2)\C)C=C1 |
MDL No. | MFCD00673917 |
别名 | Ro 13-7410; Arotinoid acid; AGN191183; TTNPB |
运输 | 蓝冰 |
InChI Key | FOIVPCKZDPCJJY-JQIJEIRASA-N |
Pubchem ID | 5289501 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, store in freezer, under -20°C |
溶解方案 |
DMSO: 7 mg/mL(20.09 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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