NP-MRD: Showing NP-Card for Enaminomycin C (NP0022036)

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Record Information

Version

2.0

Created at

2021-01-06 07:15:46 UTC

Updated at

2021-07-15 17:37:58 UTC

NP-MRD ID

NP0022036

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Enaminomycin C

Provided By

NPAtlas

Description

Enaminomycin C is found in Streptomyces, Streptomyces baarnensis No.13120 and Streptomyces fimicarius. Enaminomycin C was first documented in 1978 (PMID: 711626). Based on a literature review very few articles have been published on 2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]Hept-2-ene-3-carboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105203D          

 20 21  0  0  0  0            999 V2000
   -0.1800    2.1116   -0.6246 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2627    0.9716   -0.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8262   -0.0101   -0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2065    0.4315   -0.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1319   -0.4139   -0.1071 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5620    1.7596   -0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -1.3151   -0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5844   -2.2231   -0.1179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8532   -1.7575   -0.1000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5039   -1.8508    1.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8776   -0.8174    0.1921 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5136    0.5468    0.6590 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5107    1.4972    0.3510 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6590    2.3965   -1.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9748    2.2382    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.6969   -1.0051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1159   -2.6257   -0.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8912   -0.9503   -0.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2898    0.6364    1.7394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2360    2.0715   -0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  3  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12  2  1  0  0  0  0
 11  9  1  0  0  0  0
  1 14  1  0  0  0  0
  6 15  1  0  0  0  0
  8 16  1  0  0  0  0
  9 17  1  6  0  0  0
 11 18  1  6  0  0  0
 12 19  1  1  0  0  0
 13 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0022036

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C(O[H])[C@@]2([H])O[C@@]2([H])[C@]([H])(O[H])C1=N[H]

> <INCHI_IDENTIFIER>
InChI=1S/C7H7NO5/c8-2-1(7(11)12)3(9)5-6(13-5)4(2)10/h4-6,8-10H,(H,11,12)/b8-2+/t4-,5-,6+/m1/s1

> <INCHI_KEY>
IFMVUTNKEOCTHY-UHFFFAOYSA-N

> <FORMULA>
C7H7NO5

> <MOLECULAR_WEIGHT>
185.135

> <EXACT_MASS>
185.032422329

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
20

> <JCHEM_AVERAGE_POLARIZABILITY>
15.630011105109554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,5R,6S)-2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

> <ALOGPS_LOGP>
-1.40

> <JCHEM_LOGP>
-3.9340800183050577

> <ALOGPS_LOGS>
-1.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
5.100499710562479

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.4184339919803719

> <JCHEM_PKA_STRONGEST_BASIC>
9.840320291367355

> <JCHEM_POLAR_SURFACE_AREA>
114.14000000000001

> <JCHEM_REFRACTIVITY>
50.330400000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5R,6S)-2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

> <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  N   UNK     0      -0.180   2.112  -0.625  0.00  0.00           N+0
HETATM    2  C   UNK     0      -0.263   0.972  -0.062  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.826  -0.010  -0.081  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.207   0.432  -0.081  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.132  -0.414  -0.107  0.00  0.00           O+0
HETATM    6  O   UNK     0       2.562   1.760  -0.054  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.541  -1.315  -0.100  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.584  -2.223  -0.118  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.853  -1.758  -0.100  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.504  -1.851   1.173  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.878  -0.817   0.192  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.514   0.547   0.659  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.511   1.497   0.351  0.00  0.00           O+0
HETATM   14  H   UNK     0       0.659   2.397  -1.121  0.00  0.00           H+0
HETATM   15  H   UNK     0       2.975   2.238   0.715  0.00  0.00           H+0
HETATM   16  H   UNK     0       1.749  -2.697  -1.005  0.00  0.00           H+0
HETATM   17  H   UNK     0      -1.116  -2.626  -0.746  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.891  -0.950  -0.217  0.00  0.00           H+0
HETATM   19  H   UNK     0      -1.290   0.636   1.739  0.00  0.00           H+0
HETATM   20  H   UNK     0      -2.236   2.071  -0.414  0.00  0.00           H+0
CONECT    1    2   14                                                       
CONECT    2    1    3   12                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4   15                                                       
CONECT    7    3    8    9                                                  
CONECT    8    7   16                                                       
CONECT    9    7   10   11   17                                             
CONECT   10    9   11                                                       
CONECT   11   10   12    9   18                                             
CONECT   12   11   13    2   19                                             
CONECT   13   12   20                                                       
CONECT   14    1                                                            
CONECT   15    6                                                            
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   11                                                            
CONECT   19   12                                                            
CONECT   20   13                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

View in JSmol View NMR Assignments

Synonyms

Value	Source
2,5-Dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylate	Generator

Chemical Formula

C₇H₇NO₅

Average Mass

185.1350 Da

Monoisotopic Mass

185.03242 Da

IUPAC Name

(1S,5R,6S)-2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

Traditional Name

(1S,5R,6S)-2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C2OC2C(O)=C(C(O)=O)C1=N

InChI Identifier

InChI=1S/C7H7NO5/c8-2-1(7(11)12)3(9)5-6(13-5)4(2)10/h4-6,8-10H,(H,11,12)

InChI Key

IFMVUTNKEOCTHY-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	NPAtlas	711626
Streptomyces baarnensis No.13120	Bacteria	KNApSAcK
Streptomyces fimicarius	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-1.4	ALOGPS
logP	-3.9	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	-0.42	ChemAxon
pKa (Strongest Basic)	9.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	114.14 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	50.33 m³·mol⁻¹	ChemAxon
Polarizability	15.63 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA021096

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78444921

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139589136

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Itoh Y, Haneishi T, Arai M, Hata T, Aiba K, Tamura C: New antibiotics, enaminomycins A, B and C. III. The structures of enaminomycins A, B and C. J Antibiot (Tokyo). 1978 Sep;31(9):838-46. doi: 10.7164/antibiotics.31.838. [PubMed:711626 ]

Showing NP-Card for Enaminomycin C (NP0022036)

MOL for NP0022036 (Enaminomycin C)

3D MOL for NP0022036 (Enaminomycin C)

3D SDF for NP0022036 (Enaminomycin C)

3D-SDF for NP0022036 (Enaminomycin C)

PDB for NP0022036 (Enaminomycin C)

3D PDB for NP0022036 (Enaminomycin C)

SMILES for NP0022036 (Enaminomycin C)

INCHI for NP0022036 (Enaminomycin C)

Structure for NP0022036 (Enaminomycin C)

3D Structure for NP0022036 (Enaminomycin C)