6873-15-0
6873-15-0 structure
- Name: Arborine
- Chemical Name: 2-benzyl-1-methylquinazolin-4-one
- CAS Number: 6873-15-0
- Molecular Formula: C16H14N2O
- Molecular Weight: 250.295
- Catalog: Signaling Pathways GPCR/G Protein mAChR
- Create Date: 2017-05-28 05:17:37
- Modify Date: 2025-08-24 21:54:51
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Arborine, isolated from Glycosmis arborea, inhibits the peripheral action of acetylcholine and induces a fall in blood pressure[1][1].
| Name | 2-benzyl-1-methylquinazolin-4-one |
|---|---|
| Synonyms |
Glycosine
2-benzyl-1-methyl-1H-quinazolin-4-one 2-Benzyl-1-methyl-4(1H)-quinazolinone 1-Methyl-2-benzyl-chinazol-4-on = Arborin Glycosin 1-Methyl-2-benzyl-4(1H)-chinazolinon (Arborin) Arborin 2-BENZYL-1-METHYL-QUINAZOLIN-4-ONE 2-Benzyl-1-methylquinazolin-4(1H)-one Arborine 1-Methyl-2-benzyl-chinazolon-(4) 2-Benzyl-1-methyl-1H-chinazolin-4-on 1-Methyl-2-(phenylmethyl)-4(1H)-quinazolinone 2-Benzyl-1-methylquinazol-4-one 4(1H)-Quinazolinone, 1-methyl-2-(phenylmethyl)- |
| Description | Arborine, isolated from Glycosmis arborea, inhibits the peripheral action of acetylcholine and induces a fall in blood pressure[1][1]. |
|---|---|
| Related Catalog | |
| References |
[1]. Michael JP. Quinoline, quinazoline and acridone alkaloids. Nat Prod Rep. 2003 Oct;20(5):476-93. |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 421.0±38.0 °C at 760 mmHg |
| Molecular Formula | C16H14N2O |
| Molecular Weight | 250.295 |
| Flash Point | 208.4±26.8 °C |
| Exact Mass | 250.110611 |
| PSA | 34.89000 |
| LogP | 2.25 |
| Vapour Pressure | 0.0±1.0 mmHg at 25°C |
| Index of Refraction | 1.622 |
|
~41%
6873-15-0 |
| Literature: Chakraborty, D. P.; Mandal, Anchal Kanti; Roy, Swapan Kumar Synthesis, 1981 , # 12 p. 977 - 979 |
|
~%
6873-15-0 |
| Literature: Chatterjee; Majumdar Journal of the American Chemical Society, 1953 , vol. 75, p. 4365 |
|
~%
6873-15-0 |
| Literature: Chakrabarty, Manas; Chakravarty, Ajit K.; Pakrashi, Satyesh C. Heterocycles, 1983 , vol. 20, # 3 p. 445 - 450 |
|
~%
6873-15-0 |
| Literature: Chakrabarty, Manas; Chakravarty, Ajit K.; Pakrashi, Satyesh C. Heterocycles, 1983 , vol. 20, # 3 p. 445 - 450 |
|
~%
6873-15-0 |
| Literature: Chakravarti et al. Journal of the Chemical Society, 1953 , p. 3338 Tetrahedron, 1961 , vol. 16, p. 224,225 |
|
~%
6873-15-0 |
| Literature: Chakravarti et al. Journal of the Chemical Society, 1953 , p. 3338 Tetrahedron, 1961 , vol. 16, p. 224,225 |
| Precursor 5 | |
|---|---|
| DownStream 0 | |