Name | 3-Methoxybenzamide |
Synonyms | 3-MBA 3-ANISAMIDE m-Anisamide M-ANISAMIDE 3-Methoxybenzamide 3-methoxy-benzamid M-METHOXYBENZAMIDE 3-METHOXYBENZAMIDE Benzamide, 3-methoxy- 3-Methoxybenzamide, (m-Anisamide) |
CAS | 5813-86-5 |
EINECS | 227-379-7 |
InChI | InChI=1/C8H9NO2/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5H,1H3,(H2,9,10) |
Molecular Formula | C8H9NO2 |
Molar Mass | 151.16 |
Density | 1.143±0.06 g/cm3(Predicted) |
Melting Point | 132.5-135.5 °C (lit.) |
Boling Point | 280.0±23.0 °C(Predicted) |
Flash Point | 146.8°C |
Water Solubility | Soluble in water. |
Vapor Presure | 0.00388mmHg at 25°C |
BRN | 2206857 |
pKa | 15.81±0.50(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.546 |
MDL | MFCD00007986 |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
RTECS | CV5463333 |
biological activity | 3-Methoxybenzamide (3-MBA) is an inhibitor of ADP-ribosyltransferase (ADPRTs) and PARP, inhibition of cell division by Bacillus subtilis leads to eventual lysis of the cells. 3-Methoxybenzamide (3-MBA) can promote the growth, microtumescence and transformation efficiency of the plants of Solanum tuberosa L. subsp. andigenum. |
Target | Value |
poly(ADP-ribose) synthetase () | 2 μM |
Cell Line: | ftsZ mutant strains. |
Concentration: | 0-30 mM. |
Incubation Time: | 30℃ overnight. |
Result: | Changes directly or indirectly the ability of ftsZ to bind or hydrolyze the guanine nucleotide, ultimately leading to the inhibition of Zring formation. |