NP-MRD: Showing NP-Card for U-77864 (NP0005128)

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Record Information

Version

2.0

Created at

2020-12-09 02:28:07 UTC

Updated at

2021-07-15 16:51:07 UTC

NP-MRD ID

NP0005128

Secondary Accession Numbers

None

Natural Product Identification

Common Name

U-77864

Provided By

NPAtlas

Description

U-77864 is found in Streptomyces griseoluteus. U-77864 was first documented in 1992 (PMID: 1490873). Based on a literature review very few articles have been published on 3-hydroxy-3-(2-methylphenyl)propanimidic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118173D          

 26 26  0  0  0  0            999 V2000
   -0.6505    2.0530    0.9031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4731    0.8555    0.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8286    0.7493    0.7891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5422   -0.4229    0.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8238   -1.5002    0.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781   -1.3992   -0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7455   -0.2510    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6610   -0.2916    0.1992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9622   -1.6601    0.6664 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5371   -0.1508   -0.9704 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9349   -0.3143   -0.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0120    0.2415   -1.2266 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1912   -0.9322    0.5891 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3263    2.5218   -0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3121    2.8242    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1740    1.9229    1.5932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3617    1.6503    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5902   -0.4378    0.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4067   -2.4393   -0.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9754   -2.2990   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0841    0.2588    1.0814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0797   -2.2348   -0.1404 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4192   -0.7203   -1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386    1.0002   -1.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6390   -0.3018   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2812    1.2778   -1.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  7  2  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  3 17  1  0  0  0  0
  4 18  1  0  0  0  0
  5 19  1  0  0  0  0
  6 20  1  0  0  0  0
  8 21  1  1  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 12 25  1  0  0  0  0
 12 26  1  0  0  0  0
M  END


  Mrv1652306242118173D          

 26 26  0  0  0  0            999 V2000
   -0.6505    2.0530    0.9031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4731    0.8555    0.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8286    0.7493    0.7891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5422   -0.4229    0.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8238   -1.5002    0.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781   -1.3992   -0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7455   -0.2510    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6610   -0.2916    0.1992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9622   -1.6601    0.6664 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5371   -0.1508   -0.9704 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9349   -0.3143   -0.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0120    0.2415   -1.2266 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1912   -0.9322    0.5891 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3263    2.5218   -0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3121    2.8242    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1740    1.9229    1.5932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3617    1.6503    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5902   -0.4378    0.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4067   -2.4393   -0.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9754   -2.2990   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0841    0.2588    1.0814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0797   -2.2348   -0.1404 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4192   -0.7203   -1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386    1.0002   -1.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6390   -0.3018   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2812    1.2778   -1.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  7  2  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  3 17  1  0  0  0  0
  4 18  1  0  0  0  0
  5 19  1  0  0  0  0
  6 20  1  0  0  0  0
  8 21  1  1  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 12 25  1  0  0  0  0
 12 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005128

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]([H])(C1=C([H])C([H])=C([H])C([H])=C1C([H])([H])[H])C([H])([H])C(=O)N([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C10H13NO2/c1-7-4-2-3-5-8(7)9(12)6-10(11)13/h2-5,9,12H,6H2,1H3,(H2,11,13)/t9-/m0/s1

> <INCHI_KEY>
LKTRKUPEDMMAQL-UHFFFAOYSA-N

> <FORMULA>
C10H13NO2

> <MOLECULAR_WEIGHT>
179.219

> <EXACT_MASS>
179.094628663

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
26

> <JCHEM_AVERAGE_POLARIZABILITY>
19.47128326390284

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-3-hydroxy-3-(2-methylphenyl)propanamide

> <ALOGPS_LOGP>
0.44

> <JCHEM_LOGP>
0.6871379389999996

> <ALOGPS_LOGS>
-1.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.700484573780518

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.266192109903653

> <JCHEM_PKA_STRONGEST_BASIC>
-2.656474593127003

> <JCHEM_POLAR_SURFACE_AREA>
63.32

> <JCHEM_REFRACTIVITY>
50.191500000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.97e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-hydroxy-3-(2-methylphenyl)propanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.651   2.053   0.903  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.473   0.856   0.657  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.829   0.749   0.789  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.542  -0.423   0.472  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.824  -1.500   0.008  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.478  -1.399  -0.130  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.746  -0.251   0.184  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.661  -0.292   0.199  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.962  -1.660   0.666  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.537  -0.151  -0.970  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.935  -0.314  -0.482  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.012   0.242  -1.227  0.00  0.00           N+0
HETATM   13  O   UNK     0       3.191  -0.932   0.589  0.00  0.00           O+0
HETATM   14  H   UNK     0      -0.326   2.522  -0.107  0.00  0.00           H+0
HETATM   15  H   UNK     0      -1.312   2.824   1.326  0.00  0.00           H+0
HETATM   16  H   UNK     0       0.174   1.923   1.593  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.362   1.650   1.173  0.00  0.00           H+0
HETATM   18  H   UNK     0      -4.590  -0.438   0.613  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.407  -2.439  -0.213  0.00  0.00           H+0
HETATM   20  H   UNK     0      -0.975  -2.299  -0.499  0.00  0.00           H+0
HETATM   21  H   UNK     0       1.084   0.259   1.081  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.080  -2.235  -0.140  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.419  -0.720  -1.865  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.539   1.000  -1.179  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.639  -0.302  -1.891  0.00  0.00           H+0
HETATM   26  H   UNK     0       4.281   1.278  -1.148  0.00  0.00           H+0
CONECT    1    2   14   15   16                                             
CONECT    2    1    3    7                                                  
CONECT    3    2    4   17                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6   19                                                  
CONECT    6    5    7   20                                                  
CONECT    7    6    8    2                                                  
CONECT    8    7    9   10   21                                             
CONECT    9    8   22                                                       
CONECT   10    8   11   23   24                                             
CONECT   11   10   12   13                                                  
CONECT   12   11   25   26                                                  
CONECT   13   11                                                            
CONECT   14    1                                                            
CONECT   15    1                                                            
CONECT   16    1                                                            
CONECT   17    3                                                            
CONECT   18    4                                                            
CONECT   19    5                                                            
CONECT   20    6                                                            
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   10                                                            
CONECT   25   12                                                            
CONECT   26   12                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Hydroxy-3-(2-methylphenyl)propanimidate	Generator
3-Hydroxy-3-(2'-methylphenyl)propane-1-carboxamide	MeSH

Chemical Formula

C₁₀H₁₃NO₂

Average Mass

179.2190 Da

Monoisotopic Mass

179.09463 Da

IUPAC Name

(3S)-3-hydroxy-3-(2-methylphenyl)propanamide

Traditional Name

(3S)-3-hydroxy-3-(2-methylphenyl)propanamide

CAS Registry Number

Not Available

SMILES

CC1=CC=CC=C1C(O)CC(N)=O

InChI Identifier

InChI=1S/C10H13NO2/c1-7-4-2-3-5-8(7)9(12)6-10(11)13/h2-5,9,12H,6H2,1H3,(H2,11,13)

InChI Key

LKTRKUPEDMMAQL-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces griseoluteus	NPAtlas	1490873

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as toluenes. These are compounds containing a benzene ring which bears a methane group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Toluenes

Direct Parent

Toluenes

Alternative Parents

Substituents

Toluene
Fatty amide
Fatty acyl
Carboxamide group
Primary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Organic nitrogen compound
Carbonyl group
Aromatic alcohol
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	0.44	ALOGPS
logP	0.69	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	14.27	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	63.32 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	50.19 m³·mol⁻¹	ChemAxon
Polarizability	19.47 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

NPAtlas ID

NPA010250

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

2299933

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3035779

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Harper DE, Welch DR: Isolation, purification, synthesis, and antiinvasive/antimetastatic activity of U-77863 and U-77864 from Streptomyces griseoluteus, strain WS6724. J Antibiot (Tokyo). 1992 Dec;45(12):1827-36. doi: 10.7164/antibiotics.45.1827. [PubMed:1490873 ]

Showing NP-Card for U-77864 (NP0005128)

MOL for NP0005128 (U-77864)

3D MOL for NP0005128 (U-77864)

3D SDF for NP0005128 (U-77864)

3D-SDF for NP0005128 (U-77864)

PDB for NP0005128 (U-77864)

3D PDB for NP0005128 (U-77864)

SMILES for NP0005128 (U-77864)

INCHI for NP0005128 (U-77864)

Structure for NP0005128 (U-77864)

3D Structure for NP0005128 (U-77864)