RO5263397
- Product Name
- RO5263397
- CAS No.
- 1357266-05-7
- Chemical Name
- RO5263397
- Synonyms
- RO5263397;RO5263397,RO-5263397;RO5263397, 10 mM in DMSO;Chenodeoxycholic Acid Impurity 21;(S)-4-(3-FLUORO-2-METHYLPHENYL)-4,5-DIHYDROOXAZOL-2-AMINE;(S)-4-(3-Fluoro-2-methylphenyl)-4,5-dihydrooxazole-2-amine;2-Oxazolamine, 4-(3-fluoro-2-methylphenyl)-4,5-dihydro-, (4S)-
- CBNumber
- CB93039893
- Molecular Formula
- C10H11FN2O
- Formula Weight
- 194.21
- MOL File
- 1357266-05-7.mol
RO5263397 Property
- Boiling point:
- 303.9±52.0 °C(Predicted)
- Density
- 1.32±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO : 260 mg/mL (1338.76 mM; Need ultrasonic)
- form
- powder
- pka
- 7.68±0.70(Predicted)
- color
- white to beige
- optical activity
- [α]/D +77 to +88°, c = 1.0 in methanol
- InChI
- 1S/C10H11FN2O/c1-6-7(3-2-4-8(6)11)9-5-14-10(12)13-9/h2-4,9H,5H2,1H3,(H2,12,13)/t9-/m1/s1
- InChIKey
- IOHOUWIYOVWGHV-SECBINFHSA-N
- SMILES
- NC1=N[C@@H](C2=CC=CC(F)=C2C)CO1
Safety
- WGK Germany
- WGK 3
- Storage Class
- 11 - Combustible Solids
N-Bromosuccinimide Price
- Product number
- SML2225
- Product name
- RO5263397
- Purity
- ≥98% (HPLC)
- Packaging
- 5mg
- Price
- $113
- Updated
- 2026/04/30
- Product number
- SML2225
- Product name
- RO5263397
- Purity
- ≥98% (HPLC)
- Packaging
- 25mg
- Price
- $454
- Updated
- 2026/04/30
- Product number
- orb1708657
- Product name
- RO5263397
- Purity
- 99.37%
- Packaging
- 1mg
- Price
- $80
- Updated
- 2026/05/06
- Product number
- orb1708657
- Product name
- RO5263397
- Purity
- 99.37%
- Packaging
- 5mg
- Price
- $120
- Updated
- 2026/05/06
- Product number
- orb1708657
- Product name
- RO5263397
- Purity
- 99.37%
- Packaging
- 1mlx10mM(inDMSO)
- Price
- $120
- Updated
- 2026/05/06
RO5263397 Chemical Properties,Usage,Production
Uses
RO 5263397 is a trace amine-associated receptor 1 agonist (TAAR1).
Biological Activity
RO5256390 is an orally available partial agonist th at targets trace amine-associated receptor 1 (TAAR1) with high affinity (Ki in nM = 0.9/mouse, 4.1/human, 9.1/rat, 24/monkey TARR1), potency (EC50 in nM/relative efficacy with respect to β-phenylethylamine = 1.3/0.59/mouse, 17/0.81/human, 47/0.76/rat, 251/0.85/monkey TARR1-dependent cellular cAMP production), and selectivity (by a 112-receptor/channel/transporter and a 42-enzyme panel), without agonistic activity toward mouse TAAR4-expressing cells even at a high concentration of 30 μM. When applied via oral administration (0.003-1 mg/kg), RO5256390 exhibits similar in vivo efficacy as the full agonist RO5256390 in blocking psychostimulants-induced hyperlocomotion in mice.
in vivo
RO5263397 (0.1-1.0mg/kg; p.o.; dosing at the mid-light phase (ZT6)) increases wake time at 0.3 and 1mg/kg[2].
RO5263397 (0.3 and 1.0mg/kg; p.o.) decreases NREM time in WT mice. RO5263397 (0.3 and 1.0mg/kg; p.o.; in OE mice) powerfully increases W time in OE mice for 5-6h. NREM sleep is suppressed for 4-6h and REM sleep is almost completely suppressed for 6h after all doses of RO5263397[3].
| Animal Model: | Adult 4-5-month-old male WT littermates (C57BL/6 background)[2] |
| Dosage: | 0.1, 0.3, 1mg/kg |
| Administration: | p.o.; dosing at the mid-light phase (ZT6) |
| Result: | Increased wake time at 0.3 and 1mg/kg |
RO5263397 Preparation Products And Raw materials
Raw materials
Preparation Products
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