DB-07268
- CAS No.
- 929007-72-7
- Chemical Name:
- DB-07268
- Synonyms
- DB07268;CS-2303;DB-07268;DB 07268;DB07268 (DB 07268;DB07268, 10 mM in DMSO;DB07268;DB 07268;DB-07268;2-(4-(3-hydroxyphenylamino)pyrimidin-2-ylamino)benzamide;2-[[2-[(3-Hydroxyphenyl)amino]-4-pyrimidinyl]amino]benzamide;Benzamide, 2-[[2-[(3-hydroxyphenyl)amino]-4-pyrimidinyl]amino]-
- CBNumber:
- CB32666616
- Molecular Formula:
- C17H15N5O2
- Molecular Weight:
- 321.33
- MDL Number:
- MFCD26960941
- MOL File:
- 929007-72-7.mol
- MSDS File:
- SDS
- TDS File:
- TDS
| Boiling point | 641.6±65.0 °C(Predicted) |
|---|---|
| Density | 1.427±0.06 g/cm3(Predicted) |
| storage temp. | Store at -20°C |
| solubility | insoluble in EtOH; insoluble in H2O; ≥15.2 mg/mL in DMSO |
| form | solid |
| pka | 9.66±0.10(Predicted) |
| color | White to yellow |
| FDA UNII | MU563H6ION |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H302-H315-H319 | |||||||||
| Precautionary statements | P305+P351+P338 | |||||||||
| HS Code | 2933998090 | |||||||||
| NFPA 704 |
|
DB-07268 price More Price(48)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Cayman Chemical | 22257 | DB07268 ≥98% | 929007-72-7 | 1mg | $37 | 2026-04-30 | Buy |
| Cayman Chemical | 22257 | DB07268 ≥98% | 929007-72-7 | 5mg | $132 | 2026-04-30 | Buy |
| Cayman Chemical | 22257 | DB07268 ≥98% | 929007-72-7 | 10mg | $209 | 2026-04-30 | Buy |
| Cayman Chemical | 22257 | DB07268 ≥98% | 929007-72-7 | 25mg | $479 | 2026-04-30 | Buy |
| ChemScene | CS-1562 | DB07268 99.04% | 929007-72-7 | 5mg | $114 | 2026-06-04 | Buy |
DB-07268 Chemical Properties, Uses, Production
Uses
2-[[2-[(3-Hydroxyphenyl)amino]-4-pyrimidinyl]amino]benzamide is an intermediate used in the preparation of pyrido-pyrimidinone derivatives with potential as an antidiabetic agent.
Definition
ChEBI: 2-({2-[(3-hydroxyphenyl)amino]pyrimidin-4-yl}amino)benzamide is an aminopyrimidine and a member of benzamides. It has a role as a protein kinase inhibitor.
Biological Activity
db07268 is a jnk1 inhibitor. the c-jun n-terminal kinases (jnks) are members of the mitogen-activated protein kinase family. three jnk isoforms (jnk1, 2 and 3) have been identified. there is growing evidences indicating that activation of the jnk activity is involved in a number of human disease settings. therefore, considerable efforts have been directed toward the identification of jnk inhibitors suitable for clinical development.
in vitro
the selectivity data of db07268 against a panel of kinases has been tested. results showed that db07268 had some degree of selectivity over quite a few kinases with the exceptions of plk, chk1, and ck2. although d db07268 showed submicromolar potency against these three kinases, it still appeared to exhibit at least 70- to 90-fold greater potency against jnk1 than plk, chk1, and ck2 [1].
in vivo
several analogs of db07268 were profiled in vivo. these compounds had a range of exposure in rats and mice. some had excellent brain penetration despite having poor rat pharmacokinetics, while others had a more balanced profile. unfortunately, the most potent analog exhibited poor rat pk demonstrated by a short half-life, low oral absorption and poor brain penetration. one db07268 analog likely exhibited modest rat pk with low clearance and decent oral absorption. this analog also showed modest brain penetration [1].
IC 50
9 nm for jnk1
References
[1] liu m,wang s,clampit je,gum rj,haasch dl,rondinone cm,trevillyan jm,abad-zapatero c,fry eh,sham hl,liu g. discovery of a new class of 4-anilinopyrimidines as potent c-jun n-terminal kinase inhibitors: synthesis and sar studies. bioorg med chem lett.2007 feb 1;17(3):668-72. epub 2006 nov 2.
[2] romain nol, youseung shin, xinyi song, yuanjun he, marcel koenig, weimin chen, yuan yuan ling, li lin, claudia h. ruiz, phil lograsso, michael d. cameron, derek r. duckett, theodore m. kamenecka. synthesis and sar of 4-(pyrazol-3-yl)-pyridines as novel c-jun n-terminal kinase inhibitors.bioorg med chem lett. 2011 may 1; 21(9): 2732–2735.
DB-07268 Preparation Products And Raw materials
Raw materials
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Nanjing Chemlin Chemical Co., Ltd | 025-83697070 13770331960 | info@chemlin.com.cn | China | 16306 | 64 |
| Haoyuan Chemexpress Co., Ltd. | 021-58950125 | info@chemexpress.com | China | 7545 | 61 |
| Shanghai Aladdin Bio-Chem Technology Co.,LTD | 400-6206333 13167063860 | anhua.mao@aladdin-e.com | China | 29977 | 65 |
| MedChemexpress LLC | 021-58955995 | sales@medchemexpress.cn | United States | 4853 | 58 |
| AdooQ BioScience, LLC | +1 (866) 930-6790 | info@adooq.com | United States | 2774 | 58 |
| TargetMol Chemicals Inc. | 021-021-33632979 15002134094 | marketing@targetmol.com | China | 7993 | 58 |
| Bide Pharmatech Ltd. | 400-164-7117 18317119277 | product02@bidepharm.com | China | 40000 | 60 |
| AdooQ Bioscience CHINA | 025-58849295 | info@adooq.cn | China | 2981 | 60 |
| Shanghai JiYi Biotechnology Co. Ltd. | 13621943973 | sales@shjiyipharmatech.com | China | 1166 | 55 |
| Shanghai Lollane Biological Technology Co.,Ltd. | 021-52996696，15000506266 15000506266 | China | 4859 | 55 |
