NP-MRD: Showing NP-Card for methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate (NP0262176)

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Record Information

Version

2.0

Created at

2022-09-08 04:50:24 UTC

Updated at

2022-09-08 04:50:24 UTC

NP-MRD ID

NP0262176

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

Description

Brotasic acid methyl ester belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution. Based on a literature review very few articles have been published on Brotasic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
   -7.0907   -1.3689    1.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4579   -0.0934    0.9971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2594    0.0384    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8224   -1.0346   -0.2046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5949    1.3393    0.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2729    1.2368   -0.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3151    0.4094    0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9721    0.2492   -0.5391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3230    1.5881   -0.7325 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212    1.5265   -1.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9786    0.7683   -0.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169    0.4320    0.5793 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2809    0.4450   -1.0242 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2037   -0.2555   -0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2626   -0.8582   -0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2243   -1.5495   -0.2719 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2353   -1.7068    1.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2398   -2.4217    1.7284 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1934   -1.1131    1.7715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1970   -0.4009    1.1106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5759   -1.4592    2.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8696   -1.3996    0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3787   -2.1901    0.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4131    1.8216    1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2061    2.0661   -0.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4256    0.8319   -1.6391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8634    2.2682   -0.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7312   -0.5681    0.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1358    0.9371    1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3527   -0.4408    0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1264   -0.2496   -1.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9990    2.2978   -1.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2524    2.0499    0.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4061    2.4990   -1.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9112    0.9216   -2.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5666    0.7526   -2.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3037   -0.7648   -2.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0364   -2.0076   -0.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1692   -3.4237    1.8983 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1703   -1.2184    2.8626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4213    0.0456    1.7107 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 14  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 13 36  1  0
 15 37  1  0
 16 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
M  END


  Mrv1652309082206502D          

 20 20  0  0  0  0            999 V2000
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0262176

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCCCCCC(=O)NC1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H21NO4/c1-20-15(19)7-5-3-2-4-6-14(18)16-12-8-10-13(17)11-9-12/h8-11,17H,2-7H2,1H3,(H,16,18)

> <INCHI_KEY>
BYOPEXLQTLPYBX-UHFFFAOYSA-N

> <FORMULA>
C15H21NO4

> <MOLECULAR_WEIGHT>
279.336

> <EXACT_MASS>
279.14705816

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
30.750202787322316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

> <JCHEM_LOGP>
2.656422324666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.38504311285273

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.46159812718344

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4981950999659577

> <JCHEM_POLAR_SURFACE_AREA>
75.63000000000001

> <JCHEM_REFRACTIVITY>
76.9683

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.335 -12.320   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      16.004 -13.860   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0      17.338 -11.550   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      22.673 -14.630   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Value	Source
Brotasate methyl ester	Generator

Chemical Formula

C₁₅H₂₁NO₄

Average Mass

279.3360 Da

Monoisotopic Mass

279.14706 Da

IUPAC Name

methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

Traditional Name

methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCCCCCC(=O)NC1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C15H21NO4/c1-20-15(19)7-5-3-2-4-6-14(18)16-12-8-10-13(17)11-9-12/h8-11,17H,2-7H2,1H3,(H,16,18)

InChI Key

BYOPEXLQTLPYBX-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Anilides

Direct Parent

Anilides

Alternative Parents

Substituents

Anilide
N-arylamide
Fatty acid ester
Phenol
Fatty acid methyl ester
1-hydroxy-2-unsubstituted benzenoid
Fatty acyl
Fatty amide
Methyl ester
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Carbonyl group
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.66	ChemAxon
pKa (Strongest Acidic)	9.46	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.63 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	76.97 m³·mol⁻¹	ChemAxon
Polarizability	30.75 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44549467

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate (NP0262176)

MOL for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

3D MOL for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

3D SDF for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

3D-SDF for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

PDB for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

3D PDB for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

SMILES for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

INCHI for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

Structure for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)

3D Structure for NP0262176 (methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate)