Cas no 74711-43-6 (Zaltoprofen)
Zaltoprofen Chemical and Physical Properties
Names and Identifiers
-
- 2-(10-Oxo-10,11-dihydrodibenzo[b,f]thiepin-2-yl)propanoic acid
- 10,11-Dihydro-alpha-methyl-10-oxo-dibenzo[b,f]thiepin-2-acetic acid
- Zaltoprofen
- 10,11-Dihydro-α-methyl-10-oxo-dibenzo[b,f]thiepin-2-acetic acid
- 2-(10-Oxo-10,11-dihydrodibenzo-[b,f]thiepin-2-yl)propanoic acid
- CN100
- CN-100
- 2-(10,11-Dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic Acid
- Soleton
- Zaltoprofenum
- Zaltoprofeno
- Zaltoprofene
- CN 100
- Peon
- Zaltoprofen (unspecified)
- C17H14O3S
- 2-(6-oxo-5H-benzo[b][1]benzothiepin-3-yl)propanoic acid
- DSST
- Peon (TN)
- Zaltoprofen (+-)-
- MFCD00864323
- AMY421
- FT-0656731
- NCGC00263585-01
- HMS3744O11
- Zaltoprofen [INN]
- 74711-43-6
- Tox21_113634
- GS-3949
- AKOS015895991
- Dibenzo(b,f)thiepin-2-acetic acid, 10,11-dihydro-alpha-methyl-10-oxo-
- CHEBI:32306
- DTXSID0049076
- FT-0630837
- 2-{10-oxo-2-thiatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-6-yl}propanoic acid
- 10,11-Dihydro-alpha-methyl-10-oxodibenzo(b,f)thiepin-2-acetic acid
- CCG-267450
- (+-)-2-(10,11-Dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionic acid
- Zaltoprofen (JP17/INN)
- Zaltoprofeno [INN-Spanish]
- F0001-2421
- MLS004774050
- Zaltoprofene [INN-French]
- NCGC00263585-04
- s3008
- A838204
- Z0021
- NS00037652
- AB01565848_02
- 2-(10,11-dihydro-10-oxodibenzo[b,f]thiepin-2-yl)-propionic acid
- EINECS 277-973-5
- SW219801-1
- SCHEMBL124047
- MLS006010214
- DTXCID0029002
- 10,11-dihydro-alpha-methyl-10-oxodibenzo[b,f]thiepin-2-acetic acid
- GLXC-26617
- ZC-102
- 2-(6-Oxo-5a,6-dihydrodibenzo[b,f]thiepin-3-yl)propanoic acid
- (+-)-10,11-Dihydro-alpha-methyl-10-oxodibenzo(b,f)thiepin-2-acetic acid
- NCGC00183878-01
- 10,11-Dihydro-alpha-methyl-10-oxo-dibenzo[b,f]thiepin-2-aceticacid
- Zaltoprofen [INN:JAN]
- MUXFZBHBYYYLTH-UHFFFAOYSA-N
- ZALTOPROFEN [MI]
- HMS3885E03
- ZALTOPROFEN [WHO-DD]
- AC-32652
- H8635NG3PY
- Tox21_113634_1
- Soreton
- DB06737
- CAS-74711-43-6
- SMR003500719
- D01547
- HY-B0619
- HMS3656J14
- ZALTOPROFEN [JAN]
- 2-(10,11-dihydro-10-oxodibenzo [b,f] thiepin-2-yl)propionic acid
- BCP02387
- 1166864-09-0
- ZALTOPROFEN [MART.]
- 2-(10-Oxo-10,11-dihydro-dibenzo[b,f]thiepin-2-yl)-propionic acid
- Zaltoprofen sodium salt
- UNII-H8635NG3PY
- CHEMBL1765291
- Zaltoprofenum [INN-Latin]
- 89482-00-8
- 10,11-dihydro-a-methyl-10-oxodibenzo[b,f]thiepin-2-acetic acid
- SBI-0654128.0001
- BRD-A00578795-001-04-3
- Zaltoprofen (JP18/INN)
-
- MDL: MFCD00864323
- Inchi: 1S/C17H14O3S/c1-10(17(19)20)11-6-7-15-12(8-11)9-14(18)13-4-2-3-5-16(13)21-15/h2-8,10H,9H2,1H3,(H,19,20)
- InChI Key: MUXFZBHBYYYLTH-UHFFFAOYSA-N
- SMILES: S1C2C=CC=CC=2C(CC2C=C(C=CC1=2)C(C(=O)O)C)=O
Computed Properties
- Exact Mass: 298.06600
- Monoisotopic Mass: 298.066
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 21
- Rotatable Bond Count: 2
- Complexity: 422
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 79.7
- XLogP3: 3.5
Experimental Properties
- Color/Form: No data avaiable
- Density: 1.3±0.1 g/cm3
- Melting Point: 135.0 to 139.0 deg-C
- Boiling Point: 500.5°C at 760 mmHg
- Flash Point: 256.5±30.1 °C
- Refractive Index: 1.655
- Solubility: In vitro: DMSO solubility ≥ 100 mg/ml (335.17 mm) * "≥" means soluble, but saturation unknown
- PSA: 79.67000
- LogP: 3.76470
- Merck: 10112
- Sensitiveness: Sensitive to light
- Vapor Pressure: 0.0±1.3 mmHg at 25°C
Zaltoprofen Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H302
- Warning Statement: P264-P270-P301+P312+P330-P501
- Safety Instruction: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- RTECS:HQ2526700
- Storage Condition:Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
Zaltoprofen Customs Data
- HS CODE:2934999090
- Customs Data:
China Customs Code:
2934999090Overview:
2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Zaltoprofen Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| MedChemExpress | HY-B0619-10mM*1mLinDMSO |
Zaltoprofen |
74711-43-6 | 99.65% | 10mM*1mLinDMSO |
¥880 | 2023-07-25 | |
| MedChemExpress | HY-B0619-10mg |
Zaltoprofen |
74711-43-6 | 99.28% | 10mg |
¥420 | 2025-04-16 | |
| MedChemExpress | HY-B0619-50mg |
Zaltoprofen |
74711-43-6 | 99.28% | 50mg |
¥910 | 2025-04-16 | |
| MedChemExpress | HY-B0619-100mg |
Zaltoprofen |
74711-43-6 | 99.28% | 100mg |
¥1220 | 2025-04-16 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | Z129346-5g |
Zaltoprofen |
74711-43-6 | ≥98% | 5g |
¥141.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | Z129346-100g |
Zaltoprofen |
74711-43-6 | ≥98% | 100g |
¥1932.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | Z129346-25g |
Zaltoprofen |
74711-43-6 | ≥98% | 25g |
¥604.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | Z129346-1g |
Zaltoprofen |
74711-43-6 | ≥98% | 1g |
¥81.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | Z129346-250mg |
Zaltoprofen |
74711-43-6 | ≥98% | 250mg |
¥55.90 | 2023-08-31 | |
| Fluorochem | 093329-1g |
2-(10-Oxo-10,11-dihydrodibenzo[b,f]thiepin-2-yl)propanoic acid |
74711-43-6 | 95% | 1g |
£16.00 | 2022-03-01 |
Zaltoprofen Suppliers
Zaltoprofen Related Literature
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
-
Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
-
Hui Liu,Deyong Su,Guolin Cheng,Jimin Xu,Xinyan Wang,Yuefei Hu Org. Biomol. Chem., 2010,8, 1899-1904
-
Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511
-
Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
Additional information on Zaltoprofen
Zaltoprofen: A Comprehensive Overview
Zaltoprofen, with the CAS number 74711-43-6, is a nonsteroidal anti-inflammatory drug (NSAID) that has gained significant attention in the medical community for its potent anti-inflammatory and analgesic properties. It is commonly prescribed for the management of conditions such as osteoarthritis, rheumatoid arthritis, and other inflammatory disorders. The compound's unique chemical structure and mechanism of action make it a valuable addition to the arsenal of therapeutic agents available for treating pain and inflammation.
The chemical structure of Zaltoprofen is characterized by a substituted propionamide group, which contributes to its high potency and selectivity. This structure allows Zaltoprofen to effectively inhibit cyclooxygenase (COX) enzymes, particularly COX-2, which is primarily responsible for the synthesis of prostaglandins involved in inflammation. Unlike traditional NSAIDs that non-selectively inhibit both COX-1 and COX-2, Zaltoprofen exhibits a higher degree of selectivity for COX-2, reducing the risk of gastrointestinal side effects associated with prolonged use.
Recent studies have highlighted the potential of Zaltoprofen in addressing chronic pain conditions beyond its traditional applications. For instance, research published in 2023 demonstrated its efficacy in managing post-surgical pain and reducing opioid dependence in patients undergoing major orthopedic procedures. These findings underscore the compound's versatility and its role in modern pain management strategies.
In terms of pharmacokinetics, Zaltoprofen is rapidly absorbed after oral administration, with peak plasma concentrations achieved within 1-2 hours. Its bioavailability is relatively high, making it an efficient option for patients requiring quick relief from inflammatory symptoms. The drug is metabolized primarily in the liver via cytochrome P450 enzymes, with metabolites being excreted predominantly through urine. This metabolic profile contributes to its favorable safety profile and makes it suitable for use in a wide range of patient populations.
The clinical application of Zaltoprofen extends beyond arthritis management. It has been shown to be effective in treating soft tissue injuries, such as sprains and strains, due to its potent anti-inflammatory effects. Additionally, Zaltoprofen has demonstrated promise in alleviating symptoms associated with gouty arthritis, where it helps reduce uric acid crystallization and subsequent inflammation.
One area of ongoing research focuses on optimizing dosing regimens to maximize efficacy while minimizing adverse effects. Studies are exploring the use of sustained-release formulations to improve patient compliance and reduce the frequency of administration. Furthermore, investigations into combination therapies involving Zaltoprofen and other anti-inflammatory agents are underway to enhance therapeutic outcomes for complex conditions.
From a safety perspective, Zaltoprofen generally well-tolerated by most patients. Common side effects include mild gastrointestinal discomfort and headache; however, these are typically less severe compared to those associated with non-selective NSAIDs. Long-term studies are currently being conducted to assess the compound's impact on cardiovascular health and renal function, particularly in high-risk patient populations.
In conclusion, Zaltoprofen (CAS No 74711-43-6) stands out as a highly effective anti-inflammatory agent with a robust evidence base supporting its use across various clinical settings. Its selective COX-2 inhibition mechanism, rapid onset of action, and favorable safety profile make it an invaluable tool in modern medicine. As research continues to uncover new applications and optimize therapeutic strategies involving Zaltoprofen, its role in pain management is likely to expand further.
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