Murcko scaffold
Phenyl N-phenylcarbamate scaffold
384 chemicals on CompoundList share this ring system.
- Rings
- 2
- Scaffold atoms
- 16
- Chemicals
- 384
- With full pages
- 73
Scaffold SMILES
O=C(Nc1ccccc1)Oc1ccccc1
A Bemis-Murcko scaffold is what remains of a molecule when every side chain is removed: the rings and the chains that link them. Chemicals that share a scaffold often belong to the same compound series, which helps when you look for analogues, alternative suppliers or related building blocks.
Computed from the structures of the chemicals listed here. Stereo and charges are removed before the scaffold is taken.
Chemicals with this scaffold
Open one to see its structure, properties and suppliers.
Showing 1 to 48 of 384 chemicals
4-(((4-(Bis(2-chloroethyl)amino)phenoxy)carbonyl)amino)benzoic acid
CAS 148-78-7C18H18Cl2N2O4
Desmedipham
CAS 13684-56-5C16H16N2O4
Phenmedipham
CAS 13684-63-4C16H16N2O4
Phenyl N-methyl-N-phenylcarbamate
CAS 13599-69-4C14H13NO2
Carbanilic acid, p-tolyl ester
CAS 16323-13-0C14H13NO2
M-Chlorophenyl carbanilate
CAS 16400-09-2C13H10ClNO2
Carbanilic acid, p-nitrothio-, O-(p-chlorophenyl) ester
CAS 17710-61-1C13H9ClN2O3S
p-Methyoxyphenol carbanilate
CAS 19219-48-8C14H13NO3
Phenyl N-(3-nitrophenyl)carbamate
CAS 50699-52-0C13H10N2O4
Ethyl 3-(((phenylamino)carbonyl)oxy)benzoate
CAS 37070-83-0C16H15NO4
4-(((Phenylamino)carbonyl)oxy)benzonitrile
CAS 37070-85-2C14H10N2O2
4-Acetylphenyl phenylcarbamate
CAS 37070-86-3C15H13NO3
3-(((Phenylamino)carbonyl)oxy)benzaldehyde
CAS 37070-87-4C14H11NO3
4-Formylphenyl N-phenylcarbamate
CAS 37076-88-3C14H11NO3
4-Nitrophenyl methylphenylcarbamic acid
CAS 49839-35-2C14H12N2O4
Phenyl N-phenylcarbamate
CAS 4930-03-4C13H11NO2
Phenisopham
CAS 57375-63-0C19H22N2O4
Carbamic acid, N-phenyl-, 3-diethylaminophenyl ester
CAS 86928-03-2C17H20N2O2
2,4,5-Trichlorophenyl N-phenylcarbamate
CAS 22001-41-8C13H8Cl3NO2
Phenol, 2-nitro-3,4,6-trichloro-, phenylcarbamate
CAS 14572-56-6C13H7Cl3N2O4
Phenol, 2-nitro-3,4,6-trichloro-, p-chlorocarbanilate
CAS 14628-81-0C13H6Cl4N2O4
Carbamic acid, N-(4-cyanophenyl)-, phenyl ester
CAS 71130-54-6C14H10N2O2
Carbamic acid, (3,4-dichlorophenyl)-, 4-acetylphenyl ester
CAS 85221-17-6C15H11Cl2NO3
Phenyl 3,4-dichlorocarbanilate
CAS 57148-27-3C13H9Cl2NO2
- Methyl N-(3-(phenylcarbamoyloxy)phenyl)carbamate19961-72-9C15H14N2O4
- Phenyl N-(4-chlorophenyl)carbamate50882-28-5C13H10ClNO2
- 2-Fluoro-4-(fluorosulfonyl)phenyl hydrogen (3-chlorophenyl)carbonimidate23379-26-2C13H8ClF2NO4S
- Pentachlorophenyl hydrogen phenylcarbonimidate58683-65-1C13H6Cl5NO2
- 3-(Diethylamino)phenyl (4-methoxyphenyl)carbamate86928-06-5C18H22N2O3
- Phenyl N-(P-anisyl)carbamate20950-96-3C14H13NO3
- Pentachlorophenyl hydrogen (2-chlorophenyl)carbonimidate6333-40-0C13H5Cl6NO2
- Pentachlorophenyl (4-chlorophenyl)carbamate91693-11-7C13H5Cl6NO2
- Phenyl N-(3-chlorophenyl)carbamate50699-50-8C13H10ClNO2
- 4-Chlorophenyl 3-chlorophenylcarbamate102736-21-0C13H9Cl2NO2
- 4-Nitrophenyl phenylcarbamate6320-72-5C13H10N2O4
- 5-Methyl-2-(propan-2-yl)phenyl (4-bromophenyl)carbamate6269-49-4C17H18BrNO2
- 2-Isopropyl-5-methylphenyl (2,5-dichlorophenyl)carbamate6274-14-2C17H17Cl2NO2
- 2,4-Dichlorophenyl (4-chlorophenyl)carbamate6333-31-9C13H8Cl3NO2
- 2-Hydroxy-4-[(phenoxycarbonyl)amino]benzoic acid67324-87-2C14H11NO5
- (3-Methylphenyl) N-phenylcarbamate33274-94-1C14H13NO2
- 2,5-Dimethylphenyl phenylcarbamate66018-79-9C15H15NO2
- p-Aminophenyl p-hydroxycarbanilate6232-42-4C13H12N2O3
- 4-tert-Butylphenyl phenylcarbamate66018-74-4C17H19NO2
- 5-Methyl-2-(propan-2-yl)phenyl [4-(ethanesulfonyl)phenyl]carbamate30056-90-7C19H23NO4S
- 2-Methoxyphenyl [4-(ethanesulfonyl)phenyl]carbamate30252-09-6C16H17NO5S
- 2-Methoxyphenyl [4-(dimethylsulfamoyl)phenyl]carbamate30057-11-5C16H18N2O5S
- 5-Methyl-2-(propan-2-yl)phenyl [4-(dimethylsulfamoyl)phenyl]carbamate30057-09-1C19H24N2O4S
- Phenyl (4-(fluorosulfonyl)phenyl)carbamate21315-97-9C13H10FNO4S
Related scaffolds
Same ring framework with different atoms or bond orders
O=C(Nc1ccccc1)Nc1ccccc1421 chemicals
O=C(C=Cc1ccccc1)c1ccccc1389 chemicals
O=C(NCc1ccccc1)c1ccccc1260 chemicals
O=C(Cc1ccccc1)Nc1ccccc1219 chemicals
O=S(=O)(NCc1ccccc1)c1ccccc1164 chemicals
c1ccc(CNCc2ccccc2)cc1142 chemicals
S=C(Nc1ccccc1)Nc1ccccc1109 chemicals
O=C(CCc1ccccc1)c1ccccc187 chemicals
C(=NNc1ccccc1)c1ccccc173 chemicals
O=C(OCc1ccccc1)N1CCCCC161 chemicals
O=C(OCc1ccccc1)c1ccccc157 chemicals
O=C(Nc1ccccc1)Nc1ccccn153 chemicals