Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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P106338-25g
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25g |
1
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$62.90
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P106338-100g
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100g |
3
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$225.90
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P106338-500g
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500g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
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$1,015.90
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Non-competitive type I iodothyronine deiodinase inhibitor. Thyroperoxidase inhibitor.
| Synonyms | 6-PTU | BSPBio_000387 | PROPYLTHIOURACIL [IARC] | PROPYLTHIOURACIL [EP MONOGRAPH] | Propylthiouracil; 2,3-dihydro-6-propyl-2-thioxopyrimidin-4(1H)-one | Propylthiouracilum [INN-Latin] | 6-propyl-2-thioxo-1H-pyrimidin-4-one | AI3-25477 | Propylthiorit | Pr |
|---|---|
| Specifications & Purity | Moligand™, ≥98% |
| Biochemical and Physiological Mechanisms | Non-competitive type I iodothyronine deiodinase inhibitor (IC 50 = 0.2 μM). Thyroperoxidase inhibitor. Inhibits 5'-deiodinase peripherally. Reduces the production of thyroxine in vivo. Centrally active. |
| Shipped In | Normal |
| Grade | Moligand™ |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
| Product Description |
6-PTU is a thiolated uracil derivativewhich has been shown to acts as an antihyperthyroid agent. 6-Propyl-2-thiouracil is known to inhibit the deiodination of thyroxine to triiodothyronine via deiodinase, iodothyronine, type I (DIO1). |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Diazines |
| Subclass | Pyrimidines and pyrimidine derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyrimidones |
| Alternative Parents | Pyrimidinethiones 2-Thiopyrimidines Hydropyrimidines Vinylogous amides Heteroaromatic compounds Thioureas Lactams Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | 2-thiopyrimidine - Pyrimidinethione - Thiopyrimidine - Pyrimidone - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Lactam - Thiourea - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyrimidones. These are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. |
| External Descriptors | a small molecule |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 488191003 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488191003 |
| IUPAC Name | 6-propyl-2-sulfanylidene-1H-pyrimidin-4-one |
| INCHI | InChI=1S/C7H10N2OS/c1-2-3-5-4-6(10)9-7(11)8-5/h4H,2-3H2,1H3,(H2,8,9,10,11) |
| InChIKey | KNAHARQHSZJURB-UHFFFAOYSA-N |
| Smiles | CCCC1=CC(=O)NC(=S)N1 |
| Isomeric SMILES | CCCC1=CC(=O)NC(=S)N1 |
| WGK Germany | 3 |
| RTECS | YR1400000 |
| Molecular Weight | 170.23 |
| Beilstein | 130039 |
| Reaxy-Rn | 130039 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=130039&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 17, 2024 | P106338 | |
| Certificate of Analysis | Jul 18, 2022 | P106338 | |
| Certificate of Analysis | Jul 18, 2022 | P106338 | |
| Certificate of Analysis | Jul 18, 2022 | P106338 | |
| Certificate of Analysis | Jul 18, 2022 | P106338 |
| Solubility | Soluble in 10% ammonia, water (1.1 mg/ml) at 20 °C, DMSO, methanol, 1 N NaOH (50 mg/ml), aclcohol (16 mg/ml), and water (10 mg/ml,boiling). Insoluble in ether, chloroform, and benzene. |
|---|---|
| Sensitivity | light sensitive |
| Flash Point(°F) | 300 °C |
| Flash Point(°C) | 300°C |
| Melt Point(°C) | 218-221°C |
| Molecular Weight | 170.230 g/mol |
| XLogP3 | 0.800 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 170.051 Da |
| Monoisotopic Mass | 170.051 Da |
| Topological Polar Surface Area | 73.200 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 222.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Yongjie Zhang, Luyao Feng, Jingyan Luan, Guomei Zhang, Ning Sheng, Jinglin Shen. (2023) A cooperative effect of copper-induction and AIE leading to bright luminescence of gold nanoclusters. Inorganic Chemistry Frontiers, 11 (1): (237-245). |
| 2. Yanmin Shen, Yu Bi, Peixia Zhao, Xiaolong Yang, Zheng Zhang, Dan Dang, Han Wang, Wenju Liu. (2023) Equilibrium solubility of 6-propyl-2-thiouracil in nine pure solvents: Determination, correlation, Hansen solubility parameter and thermodynamic properties. JOURNAL OF THE INDIAN CHEMICAL SOCIETY, 100 (100934). |
| 3. Wenju Liu, Yanmin Shen, Fankun Zeng, Shuanghui Lu, Jun Li, Jinjin Yang, Kewen Zhang. (2021) Solubility Measurement and Model Correlating of 6-Propyl-2-Thiouracil in Four Binary Solvents at 278.15–323.15 K. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 66 (6): (2436–2448). |