ChemicalBook > CAS DataBase List > JNJ-10397049
JNJ-10397049
- Product Name
- JNJ-10397049
- CAS No.
- 708275-58-5
- Chemical Name
- JNJ-10397049
- Synonyms
- JNJ-10397049;JNJ-10397049, CID 9869934;JNJ 10397049; JNJ10397049;1-(2,4-dibromophenyl)-3-((4S,5S)-2,2-dimethyl-4-phenyl-1,3-dioxan-6-yl)urea;1-(2,4-dibromophenyl)-3-[(4S,5S)-2,2-dimethyl-4-phenyl-1,3-dioxan-5-yl]urea;3-(2,4-DIBROMOPHENYL)-1-[(4S,5S)-2,2-DIMETHYL-4-PHENYL-1,3-DIOXAN-5-YL]UREA;N-(2,4-DIBROMOPHENYL)-N'-[(4S,5S)-2,2-DIMETHYL-4-PHENYL-1,3-DIOXAN-5-YL]-UREA;Urea, N-(2,4-dibromophenyl)-N'-[(4S,5S)-2,2-dimethyl-4-phenyl-1,3-dioxan-5-yl]-
- CBNumber
- CB92563461
- Molecular Formula
- C19H20Br2N2O3
- Formula Weight
- 484.18
- MOL File
- 708275-58-5.mol
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JNJ-10397049 Property
- storage temp.
- Store at -20°C
- solubility
- Soluble to 100 mM in DMSO and to 100 mM in ethanol
- form
- Powder
- color
- White to off-white
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N-Bromosuccinimide Price
Cayman Chemical
- Product number
- 14139
- Product name
- JNJ-10397049
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $49
- Updated
- 2024/03/01
Cayman Chemical
- Product number
- 14139
- Product name
- JNJ-10397049
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $168
- Updated
- 2024/03/01
Cayman Chemical
- Product number
- 14139
- Product name
- JNJ-10397049
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $238
- Updated
- 2024/03/01
Tocris
- Product number
- 4317
- Product name
- JNJ10397049
- Purity
- ≥99%(HPLC)
- Packaging
- 10
- Price
- $227
- Updated
- 2021/12/16
Tocris
- Product number
- 4317
- Product name
- JNJ10397049
- Purity
- ≥99%(HPLC)
- Packaging
- 50
- Price
- $952
- Updated
- 2021/12/16
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JNJ-10397049 Chemical Properties,Usage,Production
Uses
JNJ 10397049 is a selective OX2 receptor antagonist that exhibited sleep promoting effects in rats.
in vivo
JNJ-10397049 (10-30 mg/kg) decreases the latency for persistent sleep and increased nonrapid eye movement and rapid eye movement sleep time[2].
JNJ-10397049 blocks ethanol self-administration, place preference and reinstatement[3].
| Animal Model: | Male Sprague-Dawley rats[2]. |
| Dosage: | 10 mg/kg. |
| Administration: | Subcutaneous administration. |
| Result: | Induced a significant reduction in NREM sleep latency and an increase in NREM sleep duration during the first 2 h after administration relative to vehicle treatment. |
IC 50
OX2 Receptor
storage
Store at +4°C
JNJ-10397049 Preparation Products And Raw materials
Raw materials
Preparation Products
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JNJ-10397049 Suppliers
- Tel
- 18210857532; 18210857532
- Fax
- 86-10-82849933
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- China
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