- Tak-715
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- $1.10 / 1g
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2025-04-17
- CAS:303162-79-0
- Min. Order: 1g
- Purity: 99.0% min
- Supply Ability: 100 tons min
- TAK-715
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- $34.00 / 1mg
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2024-11-19
- CAS:303162-79-0
- Min. Order:
- Purity: 99.69%
- Supply Ability: 10g
- Tak-715
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- $9.80 / 1.79999995231628KG
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2020-01-13
- CAS:303162-79-0
- Min. Order: 1g
- Purity: ≥99%
- Supply Ability: 100kg
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| | Tak-715 Basic information |
| Product Name: | Tak-715 | | Synonyms: | Tak-715;N-(4-(2-Ethyl-4-(3-methylphenyl)-thiazol-5-yl)pyridin-2-yl)benzamide;BenzaMide, N-[4-[2-ethyl-4-(3-Methylphenyl)-5-thiazolyl]-2-pyridinyl]-;N-(4-(2-Ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl)-2-pyridyl)benzamide;N-(4-(2-Ethyl-4-(m-tolyl)thiazol-5-yl)pyridin-2-yl)benzamide;N-[4-[2-Ethyl-4-(3-methylphenyl)-5-thiazolyl]-2-pyridinyl]benzamide;TAK-715; TAK715;CS-1566 | | CAS: | 303162-79-0 | | MF: | C24H21N3OS | | MW: | 399.51 | | EINECS: | | | Product Categories: | Inhibitors;MAPK | | Mol File: | 303162-79-0.mol |  |
| | Tak-715 Chemical Properties |
| storage temp. | Sealed in dry,2-8°C | | solubility | DMSO: >15mg/mL | | form | powder | | color | faint yellow to dark yellow |
| Hazard Codes | Xn | | Risk Statements | 22-36 | | Safety Statements | 26 | | WGK Germany | 3 | | HS Code | 2934999090 |
| | Tak-715 Usage And Synthesis |
| Uses | TAK 715 is a p38 MAPK inhibitor for p38α and p38β but not for p38γ and p38δ. | | Definition | ChEBI: N-[4-[2-ethyl-4-(3-methylphenyl)-5-thiazolyl]-2-pyridinyl]benzamide is a member of benzamides. | | Biological Activity | tak-715 is a selective inhibitor of p38 mapk with ic50 value of 7.1 nm [1].p38 mitogen-activated protein (map) kinases (p38 mapks) are a class of mitogen-activated protein kinases and play an important role in controlling cellular responses to cytokines and stress. four p38 mapks contain members, p38-α (mapk14), p38-β (mapk11), p38-γ (mapk12/erk6), and p38-δ (mapk13/sapk4), have been identified. abnormal expression of p38 mapks are correlated with a variety of chronic inflammatory diseases and their inhibitors are regarded as promising targets in clinical [1] [2].tak-715 is a potent p38 mapk inhibitor and has a different selectivity with the reported p38 mapk inhibitor vx-745. when tested with human monocytic thp-1 cells, administration of tak-715 exhibited inhibition on p38mapkα with ic50 value of 7.1 nm [1]. in hek293t, u2os, and f9 cells, tak-715 was used to inhibit p38 mapk activity and concluded that p38 mapk had no function in wnt/β-catenin signaling pathway [2].in adjuvant-induced rheumatoid arthritis rat model, administration of tak-715 at dose of 10 mg/kg significantly decreased lps-induced stimulated release of tnf-α (87.6%) by inhibiting p38 mapk activity [1]. | | in vivo | TAK-715 (compound 8h; 3-30 mg/kg; PO) significantly reduces the secondary paw volume[1].
TAK-715 (10 mg/kg; PO) has a Cmax of 0.19 μg/mL and an AUC of 1.16 μg h/mL. | Animal Model: | 7-week-old male Lewis rats with arthritis[1] | | Dosage: | 3, 10, 30 mg/kg | | Administration: | PO; single dose | | Result: | Significantly reduced the secondary paw volume (25% inhibition)
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| Animal Model: | Rat[1] | | Dosage: | 10 mg/kg (Pharmacokinetic Analysis) | | Administration: | PO | | Result: | Had a Cmax of 0.19 μg/mL and an AUC of 1.16 μg?h/mL.
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| | IC 50 | p38α: 7.1 nM (IC50); p38β: 200 nM (IC50); p38δ: >10 μM (IC50); p38γ: >10 μM (IC50); CK1δ; CK1ε | | storage | +4°C | | references | [1]. miwatashi, s., et al., novel inhibitor of p38 map kinase as an anti-tnf-alpha drug: discovery of n-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]benzamide (tak-715) as a potent and orally active anti-rheumatoid arthritis agent. j med chem, 2005. 48(19): p. 5966-79.
[2]. verkaar, f., et al., inhibition of wnt/beta-catenin signaling by p38 map kinase inhibitors is explained by cross-reactivity with casein kinase idelta/varepsilon. chem biol, 2011. 18(4): p. 485-94. |
| | Tak-715 Preparation Products And Raw materials |
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