NP-MRD: Showing NP-Card for Leptazoline C (NP0020661)

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Record Information

Version

2.0

Created at

2021-01-06 06:03:08 UTC

Updated at

2021-07-15 17:34:15 UTC

NP-MRD ID

NP0020661

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Leptazoline C

Provided By

NPAtlas

Description

(3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid belongs to the class of organic compounds known as beta hydroxy acids and derivatives. Beta hydroxy acids and derivatives are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom (3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid is a drug. Leptazoline C is found in Leptolyngbya sp. Based on a literature review very few articles have been published on (3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120373D          

 34 35  0  0  0  0            999 V2000
   -1.6076   -2.9519    0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.7337   -0.4499 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5127   -1.7815   -0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.4918    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2980    0.0298    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5190    1.3619    0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.9646    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8267    1.1594    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615   -0.1492   -0.1939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819   -0.7352   -0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2793   -2.0468   -0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.2370    0.4389 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919   -0.5517    0.3662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    0.2541   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0587    0.6577   -1.5387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6418    1.4511    0.6420 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7124    2.2957    0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0551    3.3366    0.7201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3548    1.9418   -1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -3.0727   -0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -2.7713    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0022   -3.8681    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0475   -1.6164   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.9610    0.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9146    2.9952    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8277    1.5858    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -0.7696   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983   -2.6408   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5686   -0.8764    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402   -0.3769   -0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272    0.4238   -1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    1.0554    1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911    2.0174    0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3369    1.7057   -1.0422 H   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 12  2  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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 13  2  1  0  0  0  0
 10  5  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  2 23  1  6  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 11 28  1  0  0  0  0
 13 29  1  1  0  0  0
 14 30  1  6  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 19 34  1  0  0  0  0
M  END

     RDKit          3D

 34 35  0  0  0  0  0  0  0  0999 V2000
   -1.6076   -2.9519    0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.7337   -0.4499 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5127   -1.7815   -0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.4918    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2980    0.0298    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5190    1.3619    0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.9646    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8267    1.1594    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615   -0.1492   -0.1939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819   -0.7352   -0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2793   -2.0468   -0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.2370    0.4389 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919   -0.5517    0.3662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    0.2541   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0587    0.6577   -1.5387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6418    1.4511    0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7124    2.2957    0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0551    3.3366    0.7201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3548    1.9418   -1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -3.0727   -0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -2.7713    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0022   -3.8681    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0475   -1.6164   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.9610    0.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9146    2.9952    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8277    1.5858    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -0.7696   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983   -2.6408   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5686   -0.8764    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402   -0.3769   -0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272    0.4238   -1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    1.0554    1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911    2.0174    0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3369    1.7057   -1.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
  4 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 13  2  1  0
 10  5  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  1
 14 30  1  6
 15 31  1  0
 16 32  1  0
 16 33  1  0
 19 34  1  0
M  END


  Mrv1652306242120373D          

 34 35  0  0  0  0            999 V2000
   -1.6076   -2.9519    0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.7337   -0.4499 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5127   -1.7815   -0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.4918    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2980    0.0298    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5190    1.3619    0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.9646    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8267    1.1594    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615   -0.1492   -0.1939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819   -0.7352   -0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2793   -2.0468   -0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.2370    0.4389 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919   -0.5517    0.3662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    0.2541   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0587    0.6577   -1.5387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6418    1.4511    0.6420 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7124    2.2957    0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0551    3.3366    0.7201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3548    1.9418   -1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -3.0727   -0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -2.7713    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0022   -3.8681    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0475   -1.6164   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.9610    0.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9146    2.9952    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8277    1.5858    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -0.7696   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983   -2.6408   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5686   -0.8764    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402   -0.3769   -0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272    0.4238   -1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    1.0554    1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911    2.0174    0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3369    1.7057   -1.0422 H   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 12  2  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
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 13  2  1  0  0  0  0
 10  5  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  2 23  1  6  0  0  0
  6 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  9 27  1  0  0  0  0
 11 28  1  0  0  0  0
 13 29  1  1  0  0  0
 14 30  1  6  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 19 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0020661

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])[C@@]([H])(O[H])[C@]1([H])N=C(O[C@@]1([H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H15NO5/c1-7-12(10(16)6-11(17)18)14-13(19-7)8-4-2-3-5-9(8)15/h2-5,7,10,12,15-16H,6H2,1H3,(H,17,18)/t7-,10+,12+/m0/s1

> <INCHI_KEY>
HYNVCGWXNJDHLB-HNBZJPLGSA-N

> <FORMULA>
C13H15NO5

> <MOLECULAR_WEIGHT>
265.265

> <EXACT_MASS>
265.095022587

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
26.64875172354161

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid

> <ALOGPS_LOGP>
0.67

> <JCHEM_LOGP>
1.6236564529485151

> <ALOGPS_LOGS>
-2.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.371213981112225

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.800324291563435

> <JCHEM_PKA_STRONGEST_BASIC>
1.8218542182282624

> <JCHEM_POLAR_SURFACE_AREA>
99.35000000000001

> <JCHEM_REFRACTIVITY>
66.1534

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 35  0  0  0  0  0  0  0  0999 V2000
   -1.6076   -2.9519    0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.7337   -0.4499 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5127   -1.7815   -0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.4918    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2980    0.0298    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5190    1.3619    0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.9646    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8267    1.1594    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615   -0.1492   -0.1939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819   -0.7352   -0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2793   -2.0468   -0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.2370    0.4389 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919   -0.5517    0.3662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    0.2541   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0587    0.6577   -1.5387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6418    1.4511    0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7124    2.2957    0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0551    3.3366    0.7201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3548    1.9418   -1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -3.0727   -0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -2.7713    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0022   -3.8681    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0475   -1.6164   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.9610    0.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9146    2.9952    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8277    1.5858    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -0.7696   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983   -2.6408   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5686   -0.8764    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402   -0.3769   -0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272    0.4238   -1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    1.0554    1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911    2.0174    0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3369    1.7057   -1.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
  4 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 13  2  1  0
 10  5  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  1
 14 30  1  6
 15 31  1  0
 16 32  1  0
 16 33  1  0
 19 34  1  0
M  END

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      -1.608  -2.952   0.077  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.893  -1.734  -0.450  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.513  -1.782  -0.154  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.918  -0.492   0.135  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.298   0.030   0.116  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.519   1.362   0.437  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.750   1.965   0.456  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.827   1.159   0.127  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.662  -0.149  -0.194  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.382  -0.735  -0.203  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.279  -2.047  -0.532  0.00  0.00           O+0
HETATM   12  N   UNK     0      -0.110   0.237   0.439  0.00  0.00           N+0
HETATM   13  C   UNK     0      -1.292  -0.552   0.366  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.409   0.254  -0.255  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.059   0.658  -1.539  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.642   1.451   0.642  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.712   2.296   0.119  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.055   3.337   0.720  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.355   1.942  -1.053  0.00  0.00           O+0
HETATM   20  H   UNK     0      -2.553  -3.073  -0.496  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.884  -2.771   1.135  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.002  -3.868   0.024  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.048  -1.616  -1.536  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.658   1.961   0.689  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.915   2.995   0.705  0.00  0.00           H+0
HETATM   26  H   UNK     0       5.828   1.586   0.126  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.500  -0.770  -0.448  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.498  -2.641  -0.599  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.569  -0.876   1.381  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.340  -0.377  -0.272  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.127   0.424  -1.733  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.861   1.055   1.658  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.691   2.017   0.730  0.00  0.00           H+0
HETATM   34  H   UNK     0      -5.337   1.706  -1.042  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3   13   23                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11    5                                                  
CONECT   11   10   28                                                       
CONECT   12    4   13                                                       
CONECT   13   12   14    2   29                                             
CONECT   14   13   15   16   30                                             
CONECT   15   14   31                                                       
CONECT   16   14   17   32   33                                             
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   34                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    2                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   11                                                            
CONECT   29   13                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   16                                                            
CONECT   34   19                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   70    0
END

RDKit          3D

34 35  0  0  0  0  0  0  0  0999 V2000
   -1.6076   -2.9519    0.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.7337   -0.4499 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5127   -1.7815   -0.1544 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -0.4918    0.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2980    0.0298    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5190    1.3619    0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.9646    0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8267    1.1594    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615   -0.1492   -0.1939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3819   -0.7352   -0.2031 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2793   -2.0468   -0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1103    0.2370    0.4389 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919   -0.5517    0.3662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    0.2541   -0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0587    0.6577   -1.5387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6418    1.4511    0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7124    2.2957    0.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0551    3.3366    0.7201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3548    1.9418   -1.0527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -3.0727   -0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8837   -2.7713    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0022   -3.8681    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0475   -1.6164   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.9610    0.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9146    2.9952    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8277    1.5858    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005   -0.7696   -0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983   -2.6408   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5686   -0.8764    1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402   -0.3769   -0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272    0.4238   -1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    1.0554    1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6911    2.0174    0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3369    1.7057   -1.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
  4 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 13  2  1  0
 10  5  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 11 28  1  0
 13 29  1  1
 14 30  1  6
 15 31  1  0
 16 32  1  0
 16 33  1  0
 19 34  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(3R)-3-Hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoate	Generator

Chemical Formula

C₁₃H₁₅NO₅

Average Mass

265.2650 Da

Monoisotopic Mass

265.09502 Da

IUPAC Name

(3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid

Traditional Name

(3R)-3-hydroxy-3-[(4S,5S)-2-(2-hydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1OC(=N[C@H]1[C@H](O)CC(O)=O)C1=CC=CC=C1O

InChI Identifier

InChI=1S/C13H15NO5/c1-7-12(10(16)6-11(17)18)14-13(19-7)8-4-2-3-5-9(8)15/h2-5,7,10,12,15-16H,6H2,1H3,(H,17,18)/t7-,10+,12+/m0/s1

InChI Key

HYNVCGWXNJDHLB-HNBZJPLGSA-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
Leptolyngbya sp.	NPAtlas	31591889

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta hydroxy acids and derivatives. Beta hydroxy acids and derivatives are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Hydroxy acids and derivatives

Sub Class

Beta hydroxy acids and derivatives

Direct Parent

Beta hydroxy acids and derivatives

Alternative Parents

Substituents

1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Beta-hydroxy acid
Benzenoid
Monocyclic benzene moiety
Oxazoline
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	0.67	ALOGPS
logP	1.62	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	3.8	ChemAxon
pKa (Strongest Basic)	1.82	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.35 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	66.15 m³·mol⁻¹	ChemAxon
Polarizability	26.65 Å³	ChemAxon
Number of Rings	2	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

NPA026851

HMDB ID

Not Available

DrugBank ID

DB15553

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

81361128

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145994625

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Leptazoline C (NP0020661)

MOL for NP0020661 (Leptazoline C)

3D MOL for NP0020661 (Leptazoline C)

3D SDF for NP0020661 (Leptazoline C)

3D-SDF for NP0020661 (Leptazoline C)

PDB for NP0020661 (Leptazoline C)

3D PDB for NP0020661 (Leptazoline C)

SMILES for NP0020661 (Leptazoline C)

INCHI for NP0020661 (Leptazoline C)

Structure for NP0020661 (Leptazoline C)

3D Structure for NP0020661 (Leptazoline C)