NP-MRD: Showing NP-Card for (2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid (NP0156018)

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Record Information

Version

2.0

Created at

2022-09-02 13:10:28 UTC

Updated at

2022-09-02 13:10:28 UTC

NP-MRD ID

NP0156018

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid

Description

(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. (2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid is found in Streptomyces cyaneofuscatus. Based on a literature review very few articles have been published on (2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215102D          

 25 27  0  0  1  0            999 V2000
   -4.7370    1.3537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9165    1.4399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5810    2.1936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4316    0.7725    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7671    0.0188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2822   -0.6486    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111    0.8587    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    0.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4617   -0.5624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3057    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8932    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0862    0.8205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537   -0.3356    0.0000 N   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  1  1  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 14 23  2  0  0  0  0
 23 24  1  0  0  0  0
 13 25  2  0  0  0  0
 10 25  1  0  0  0  0
M  END

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    6.8900   -1.1566   -0.9247 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6727   -0.8812   -1.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7618   -1.9190   -1.0336 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1884    0.5139   -1.1220 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7737    1.4146   -0.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3920    0.8885    1.6197 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.7713    0.5747   -1.1471 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9053    0.0691   -0.3813 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2634   -0.6939    0.7011 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4942    0.2938   -0.6426 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9164    1.0210   -1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782    0.9616   -1.5214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7100    0.2319   -0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1044   -0.0239   -0.0271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    0.5139   -0.7572 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3757    0.3191   -0.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4229    0.8716   -1.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7425    0.6759   -0.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0735   -0.0805    0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0614   -0.6315    1.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7153   -0.4368    0.6822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7248   -0.9945    1.4412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3913   -0.7802    1.0741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418   -1.3587    1.8650 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4453   -0.1632    0.0613 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0365   -2.8875   -0.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5238    0.8890   -2.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8935    1.3458   -0.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5212    2.4727   -0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1412   -0.2428    1.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7170   -0.5472    1.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913    1.5367   -2.4314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2000    1.4616   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5591    1.1104   -1.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1117   -0.2500    0.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2420   -1.2308    1.8920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680   -1.5936    2.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4749   -1.2937    1.7289 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 25  2  0
 13 14  1  0
 14 23  2  0
 23 24  1  0
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 25 10  1  0
 15 14  1  0
 16 21  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  5 29  1  0
  6 30  1  0
  9 31  1  0
 11 32  1  0
 24 38  1  0
 22 37  1  0
 20 36  1  0
 19 35  1  0
 18 34  1  0
 17 33  1  0
M  END


  Mrv1652309022215102D          

 25 27  0  0  1  0            999 V2000
   -4.7370    1.3537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9165    1.4399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5810    2.1936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4316    0.7725    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7671    0.0188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2822   -0.6486    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6111    0.8587    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    0.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4617   -0.5624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3057    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8932    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0862    0.8205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537   -0.3356    0.0000 N   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  1  1  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 14 23  2  0  0  0  0
 23 24  1  0  0  0  0
 13 25  2  0  0  0  0
 10 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156018

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)[C@H](CS)N=C(O)C1=COC(=N1)C1=C(O)C=C2C=CC=CC2=N1

> <INCHI_IDENTIFIER>
InChI=1S/C16H13N3O5S/c20-12-5-8-3-1-2-4-9(8)17-13(12)15-19-10(6-24-15)14(21)18-11(7-25)16(22)23/h1-6,11,20,25H,7H2,(H,18,21)(H,22,23)/t11-/m0/s1

> <INCHI_KEY>
RBQMFLPOEYGTJP-NSHDSACASA-N

> <FORMULA>
C16H13N3O5S

> <MOLECULAR_WEIGHT>
359.36

> <EXACT_MASS>
359.057591705

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
35.49889412913871

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid

> <ALOGPS_LOGP>
2.32

> <JCHEM_LOGP>
2.5549174419999994

> <ALOGPS_LOGS>
-3.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.398072055609233

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6293330230901986

> <JCHEM_PKA_STRONGEST_BASIC>
0.03403252817689573

> <JCHEM_POLAR_SURFACE_AREA>
129.04000000000002

> <JCHEM_REFRACTIVITY>
99.8288

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0      -8.842   2.527   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -7.311   2.688   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -6.684   4.095   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -6.406   1.442   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.032   0.035   0.000  0.00  0.00           C+0
HETATM    6  S   UNK     0      -6.127  -1.211   0.000  0.00  0.00           S+0
HETATM    7  N   UNK     0      -4.874   1.603   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -3.969   0.357   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.595  -1.050   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.437   0.518   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.667   1.852   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.161   1.532   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       2.667   0.000   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0      -1.407  -0.626   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   25                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   25                                                  
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   14   24                                                  
CONECT   24   23                                                            
CONECT   25   13   10                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoate	Generator
(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulphanylpropanoate	Generator
(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulphanylpropanoic acid	Generator

Chemical Formula

C₁₆H₁₃N₃O₅S

Average Mass

359.3600 Da

Monoisotopic Mass

359.05759 Da

IUPAC Name

(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid

Traditional Name

(2R)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)[C@H](CS)N=C(O)C1=COC(=N1)C1=C(O)C=C2C=CC=CC2=N1

InChI Identifier

InChI=1S/C16H13N3O5S/c20-12-5-8-3-1-2-4-9(8)17-13(12)15-19-10(6-24-15)14(21)18-11(7-25)16(22)23/h1-6,11,20,25H,7H2,(H,18,21)(H,22,23)/t11-/m0/s1

InChI Key

RBQMFLPOEYGTJP-NSHDSACASA-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

Species Name	Source	Reference
Streptomyces cyaneofuscatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids

Alternative Parents

Substituents

N-acyl-alpha-amino acid
Cysteine or derivatives
Hydroxyquinoline
Quinoline
Hydroxypyridine
2,4-disubstituted 1,3-oxazole
Benzenoid
Pyridine
Heteroaromatic compound
Oxazole
Azole
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboximidic acid derivative
Carboximidic acid
Alkylthiol
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.32	ALOGPS
logP	2.55	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.63	ChemAxon
pKa (Strongest Basic)	0.034	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	129.04 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	99.83 m³·mol⁻¹	ChemAxon
Polarizability	35.5 Å³	ChemAxon
Number of Rings	3	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

71048866

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

156581810

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid (NP0156018)

MOL for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

3D MOL for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

3D SDF for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

3D-SDF for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

PDB for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

3D PDB for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

SMILES for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

INCHI for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

Structure for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)

3D Structure for NP0156018 ((2r)-2-({hydroxy[2-(3-hydroxyquinolin-2-yl)-1,3-oxazol-4-yl]methylidene}amino)-3-sulfanylpropanoic acid)