NP-MRD: Showing NP-Card for SPF32629B (NP0006261)

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Record Information

Version

2.0

Created at

2020-12-09 03:17:36 UTC

Updated at

2021-07-15 16:54:17 UTC

NP-MRD ID

NP0006261

Secondary Accession Numbers

None

Natural Product Identification

Common Name

SPF32629B

Provided By

NPAtlas

Description

SPF-32629B is also known as SPF 32629 b. SPF-32629B is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. SPF32629B is found in Penicillium. SPF32629B was first documented in 2006 (PMID: 16568716). Based on a literature review very few articles have been published on SPF-32629B (PMID: 21397370).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242121113D          

 44 45  0  0  0  0            999 V2000
   -5.4979   -0.3960   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4192   -0.3351   -0.4341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3888   -1.6844    0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    0.0323   -1.0990 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0071    0.1222   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1163   -0.0875    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7491    0.4544   -0.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    0.5587    0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8607    1.9610    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.6061    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    3.9112    1.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357    4.5507    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4018    3.9423   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9576    2.6263   -0.9428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397   -0.4200   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0909   -1.1584    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -2.0740    0.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -2.8002    1.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4615   -2.2942   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5056   -3.2622   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -3.4187   -2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1431   -3.9858   -0.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.5608   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288   -1.7296   -2.8498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8442   -0.6649   -1.3560 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4881   -0.4103   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7481    0.4002    0.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -2.4952   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4568   -1.9184    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.6913    1.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2960    0.9802   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6886    2.1367   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062   -1.0021    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427   -2.6500    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7297   -3.4723    0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -0.1402   -2.1396 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
  2  4  1  0  0  0  0
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  3 32  1  0  0  0  0
  4 33  1  0  0  0  0
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  8 35  1  1  0  0  0
 10 36  1  0  0  0  0
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 16 41  1  0  0  0  0
 18 42  1  0  0  0  0
 22 43  1  0  0  0  0
 25 44  1  0  0  0  0
M  END

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -5.4979   -0.3960   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4192   -0.3351   -0.4341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3888   -1.6844    0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    0.0323   -1.0990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0071    0.1222   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1163   -0.0875    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7491    0.4544   -0.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    0.5587    0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8607    1.9610    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.6061    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    3.9112    1.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357    4.5507    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4018    3.9423   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9576    2.6263   -0.9428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397   -0.4200   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0909   -1.1584    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -2.0740    0.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -2.8002    1.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4615   -2.2942   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5056   -3.2622   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -3.4187   -2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1431   -3.9858   -0.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.5608   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288   -1.7296   -2.8498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8442   -0.6649   -1.3560 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4881   -0.4103   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747   -1.2923   -2.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4278    0.5418   -2.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7481    0.4002    0.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -2.4952   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4568   -1.9184    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.6913    1.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2960    0.9802   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9373   -0.7389   -1.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689    0.3337    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266    2.0739    2.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9210    4.4171    2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    5.5916    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4673    4.4425   -1.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6886    2.1367   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062   -1.0021    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427   -2.6500    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7297   -3.4723    0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -0.1402   -2.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  8 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 19 23  1  0
 23 24  2  0
 23 25  1  0
 14  9  1  0
 25 15  1  0
  1 26  1  0
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  1 28  1  0
  2 29  1  1
  3 30  1  0
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  3 32  1  0
  4 33  1  0
  4 34  1  0
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 14 40  1  0
 16 41  1  0
 18 42  1  0
 22 43  1  0
 25 44  1  0
M  END


  Mrv1652306242121113D          

 44 45  0  0  0  0            999 V2000
   -5.4979   -0.3960   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4192   -0.3351   -0.4341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3888   -1.6844    0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    0.0323   -1.0990 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0071    0.1222   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1163   -0.0875    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7491    0.4544   -0.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    0.5587    0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8607    1.9610    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.6061    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    3.9112    1.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357    4.5507    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4018    3.9423   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9576    2.6263   -0.9428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397   -0.4200   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0909   -1.1584    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -2.0740    0.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -2.8002    1.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4615   -2.2942   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5056   -3.2622   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -3.4187   -2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1431   -3.9858   -0.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.5608   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288   -1.7296   -2.8498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8442   -0.6649   -1.3560 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3747   -1.2923   -2.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7481    0.4002    0.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -2.4952   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4568   -1.9184    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.6913    1.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2960    0.9802   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9373   -0.7389   -1.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689    0.3337    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266    2.0739    2.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9210    4.4171    2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    5.5916    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4673    4.4425   -1.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6886    2.1367   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062   -1.0021    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427   -2.6500    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7297   -3.4723    0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -0.1402   -2.1396 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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  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
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
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 17 19  2  0  0  0  0
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 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 14  9  1  0  0  0  0
 25 15  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  2 29  1  1  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  3 32  1  0  0  0  0
  4 33  1  0  0  0  0
  4 34  1  0  0  0  0
  8 35  1  1  0  0  0
 10 36  1  0  0  0  0
 11 37  1  0  0  0  0
 12 38  1  0  0  0  0
 13 39  1  0  0  0  0
 14 40  1  0  0  0  0
 16 41  1  0  0  0  0
 18 42  1  0  0  0  0
 22 43  1  0  0  0  0
 25 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006261

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO6/c1-10(2)8-14(21)25-16(11-6-4-3-5-7-11)12-9-13(20)15(18(23)24)17(22)19-12/h3-7,9-10,16H,8H2,1-2H3,(H,23,24)(H2,19,20,22)/t16-/m1/s1

> <INCHI_KEY>
RQSUJBPFSUWQSA-UHFFFAOYSA-N

> <FORMULA>
C18H19NO6

> <MOLECULAR_WEIGHT>
345.351

> <EXACT_MASS>
345.121237336

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.20567628990153

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-6-[(R)-[(3-methylbutanoyl)oxy](phenyl)methyl]-2-oxo-1,2-dihydropyridine-3-carboxylic acid

> <ALOGPS_LOGP>
2.20

> <JCHEM_LOGP>
2.0177433733333334

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.905389516953978

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.552952304348786

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8754399404358795

> <JCHEM_POLAR_SURFACE_AREA>
112.93

> <JCHEM_REFRACTIVITY>
90.58549999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.90e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-6-[(R)-[(3-methylbutanoyl)oxy](phenyl)methyl]-2-oxo-1H-pyridine-3-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -5.4979   -0.3960   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4192   -0.3351   -0.4341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3888   -1.6844    0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    0.0323   -1.0990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0071    0.1222   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1163   -0.0875    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7491    0.4544   -0.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    0.5587    0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8607    1.9610    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.6061    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    3.9112    1.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357    4.5507    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4018    3.9423   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9576    2.6263   -0.9428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397   -0.4200   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0909   -1.1584    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -2.0740    0.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -2.8002    1.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4615   -2.2942   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5056   -3.2622   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -3.4187   -2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1431   -3.9858   -0.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.5608   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288   -1.7296   -2.8498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8442   -0.6649   -1.3560 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4881   -0.4103   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747   -1.2923   -2.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4278    0.5418   -2.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7481    0.4002    0.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -2.4952   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4568   -1.9184    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.6913    1.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2960    0.9802   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9373   -0.7389   -1.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689    0.3337    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266    2.0739    2.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9210    4.4171    2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    5.5916    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4673    4.4425   -1.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6886    2.1367   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062   -1.0021    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427   -2.6500    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7297   -3.4723    0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -0.1402   -2.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  8 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 19 23  1  0
 23 24  2  0
 23 25  1  0
 14  9  1  0
 25 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  8 35  1  1
 10 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 22 43  1  0
 25 44  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      -5.498  -0.396  -1.513  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.419  -0.335  -0.434  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.389  -1.684   0.227  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.134   0.032  -1.099  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.007   0.122  -0.145  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.116  -0.088   1.092  0.00  0.00           O+0
HETATM    7  O   UNK     0      -0.749   0.454  -0.614  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.380   0.559   0.247  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.861   1.961   0.262  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.208   2.606   1.445  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.649   3.911   1.414  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.736   4.551   0.192  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.402   3.942  -0.983  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.958   2.626  -0.943  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.440  -0.420  -0.088  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.091  -1.158   0.905  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.077  -2.074   0.628  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.713  -2.800   1.642  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.462  -2.294  -0.690  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.506  -3.262  -1.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.811  -3.419  -2.208  0.00  0.00           O+0
HETATM   22  O   UNK     0       5.143  -3.986  -0.020  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.811  -1.561  -1.646  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.129  -1.730  -2.850  0.00  0.00           O+0
HETATM   25  N   UNK     0       1.844  -0.665  -1.356  0.00  0.00           N+0
HETATM   26  H   UNK     0      -6.488  -0.410  -0.997  0.00  0.00           H+0
HETATM   27  H   UNK     0      -5.375  -1.292  -2.159  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.428   0.542  -2.086  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.748   0.400   0.320  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.087  -2.495  -0.471  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.457  -1.918   0.510  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.819  -1.691   1.174  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.296   0.980  -1.652  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.937  -0.739  -1.888  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.069   0.334   1.308  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.127   2.074   2.373  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.921   4.417   2.336  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.089   5.592   0.176  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.467   4.442  -1.957  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.689   2.137  -1.887  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.806  -1.002   1.938  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.443  -2.650   2.605  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.730  -3.472   0.638  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.390  -0.140  -2.140  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3    4   29                                             
CONECT    3    2   30   31   32                                             
CONECT    4    2    5   33   34                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   15   35                                             
CONECT    9    8   10   14                                                  
CONECT   10    9   11   36                                                  
CONECT   11   10   12   37                                                  
CONECT   12   11   13   38                                                  
CONECT   13   12   14   39                                                  
CONECT   14   13    9   40                                                  
CONECT   15    8   16   25                                                  
CONECT   16   15   17   41                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   42                                                       
CONECT   19   17   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   43                                                       
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   15   44                                                  
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    4                                                            
CONECT   34    4                                                            
CONECT   35    8                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   13                                                            
CONECT   40   14                                                            
CONECT   41   16                                                            
CONECT   42   18                                                            
CONECT   43   22                                                            
CONECT   44   25                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   90    0
END

RDKit          3D

44 45  0  0  0  0  0  0  0  0999 V2000
   -5.4979   -0.3960   -1.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4192   -0.3351   -0.4341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3888   -1.6844    0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1344    0.0323   -1.0990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0071    0.1222   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1163   -0.0875    1.0919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7491    0.4544   -0.6143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3803    0.5587    0.2472 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8607    1.9610    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.6061    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494    3.9112    1.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7357    4.5507    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4018    3.9423   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9576    2.6263   -0.9428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397   -0.4200   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0909   -1.1584    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -2.0740    0.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -2.8002    1.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4615   -2.2942   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5056   -3.2622   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -3.4187   -2.2079 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1431   -3.9858   -0.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109   -1.5608   -1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288   -1.7296   -2.8498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8442   -0.6649   -1.3560 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4881   -0.4103   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3747   -1.2923   -2.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4278    0.5418   -2.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7481    0.4002    0.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -2.4952   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4568   -1.9184    0.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.6913    1.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2960    0.9802   -1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9373   -0.7389   -1.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0689    0.3337    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266    2.0739    2.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9210    4.4171    2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    5.5916    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4673    4.4425   -1.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6886    2.1367   -1.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8062   -1.0021    1.9385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4427   -2.6500    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7297   -3.4723    0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3900   -0.1402   -2.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  8 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 19 23  1  0
 23 24  2  0
 23 25  1  0
 14  9  1  0
 25 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  8 35  1  1
 10 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 22 43  1  0
 25 44  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
SPF 32629 b	MeSH
SPF-32629 b	MeSH

Chemical Formula

C₁₈H₁₉NO₆

Average Mass

345.3510 Da

Monoisotopic Mass

345.12124 Da

IUPAC Name

4-hydroxy-6-[(R)-[(3-methylbutanoyl)oxy](phenyl)methyl]-2-oxo-1,2-dihydropyridine-3-carboxylic acid

Traditional Name

4-hydroxy-6-[(R)-[(3-methylbutanoyl)oxy](phenyl)methyl]-2-oxo-1H-pyridine-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)OC(C1=CC=CC=C1)C1=CC(O)=C(C(O)=O)C(O)=N1

InChI Identifier

InChI=1S/C18H19NO6/c1-10(2)8-14(21)25-16(11-6-4-3-5-7-11)12-9-13(20)15(18(23)24)17(22)19-12/h3-7,9-10,16H,8H2,1-2H3,(H,23,24)(H2,19,20,22)

InChI Key

RQSUJBPFSUWQSA-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
Penicillium	NPAtlas	16568716

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	2.2	ALOGPS
logP	2.02	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	3.55	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	112.93 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	90.59 m³·mol⁻¹	ChemAxon
Polarizability	35.21 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

NPA005617

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26337719

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54684614

PDB ID

Not Available

ChEBI ID

66518

Good Scents ID

Not Available

References

General References

Shimatani T, Hosotani N, Ohnishi M, Kumagai K, Saji I: SPF-32629 A and B, novel human chymase inhibitors produced by Penicillium sp. J Antibiot (Tokyo). 2006 Jan;59(1):29-34. doi: 10.1038/ja.2006.5. [PubMed:16568716 ]
Vegi SR, Boovanahalli SK, Patro B, Mukkanti K: SPF32629A and SPF32629B: enantioselective synthesis, determination of absolute configuration, cytotoxicity and antibacterial evaluation. Eur J Med Chem. 2011 May;46(5):1803-12. doi: 10.1016/j.ejmech.2011.02.039. Epub 2011 Feb 23. [PubMed:21397370 ]

Showing NP-Card for SPF32629B (NP0006261)

MOL for NP0006261 (SPF32629B)

3D MOL for NP0006261 (SPF32629B)

3D SDF for NP0006261 (SPF32629B)

3D-SDF for NP0006261 (SPF32629B)

PDB for NP0006261 (SPF32629B)

3D PDB for NP0006261 (SPF32629B)

SMILES for NP0006261 (SPF32629B)

INCHI for NP0006261 (SPF32629B)

Structure for NP0006261 (SPF32629B)

3D Structure for NP0006261 (SPF32629B)