93-98-1
93-98-1
Chemical Structure
N-Phenylbenzamide
Synonym(s): N-Benzoylaniline
- CAS No.: 93-98-1
- Formula:C13H11NO
- Molecular Weight:197.24
IUPAC Name: N-phenylbenzamide
InChIKey: ZVSKZLHKADLHSD-UHFFFAOYSA-N
SMILES: O=C(NC1=CC=CC=C1)C2=CC=CC=C2
Biological Activity: N-Phenylbenzamide (N-Benzoylaniline) is a compound skeleton. N-Phenylbenzamide can be used for the researches of cancer and infection, such as enterovirus and cervical cancer[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-Phenylbenzamide | 99.94% | N-Phenylbenzamide (N-Benzoylaniline) is a compound skeleton. N-Phenylbenzamide can be used for the researches of cancer and infection, such as enterovirus and cervical cancer. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.88
HY-Y0546RBenzophenone (Standard) -
Similarity Score 0.88
HY-Y0546S2Benzophenone-13C -
Similarity Score 0.88
HY-18805Nicotinanilide -
Similarity Score 0.85
HY-N7133Diphenylamine hydrochloride -
Similarity Score 0.84
HY-W016321N-Benzylaniline -
Similarity Score 0.83
HY-W0098492-Aminobenzophenone -
Similarity Score 0.80
HY-W0769034-Aminobenzophenone -
Similarity Score 0.80
HY-W016321SN-Benzylaniline-d2 -
Similarity Score 0.79
HY-Y1067Dibenzylamine -
Explore the MedChemAI to find more analogs
References
- [1]. Jiang Z, et al. Synthesis and antiviral activity of a series of novel N-phenylbenzamide and N-phenylacetophenone compounds as anti-HCV and anti-EV71 agents. Acta Pharm Sin B. 2015 May;5(3):201-9. [Content Brief]
- [2]. Theerachayanan T, et al. SYNTHESIS AND ANTI-CANCER ACTIVITY OF 3-CHLORO-N-PHENYLBENZAMIDE. Interprof J Health Sci. 2019 Dec. 20;17(2):72-9.
