MiMeDB: Showing metabocard for Penitrem B (MMDBc0004700)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:35:15 UTC

Update Date

2022-08-31 06:22:52 UTC

Metabolite ID

MMDBc0004700

Metabolite Identification

Common Name

Penitrem B

Description

Penitrem B, also known as tremortin b or penitrems, belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on Penitrem B.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100352D          

 52 61  0  0  1  0            999 V2000
    2.0169    5.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6881    4.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1587    4.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5703    2.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5674    2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5970    5.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9389    5.5573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1629    6.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3843    6.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5053    3.3484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913    5.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7941    5.7190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7025    3.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9782    5.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5544    2.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    5.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3360    4.6701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3161    5.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8711    3.9886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0711    3.9488    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7757    3.2718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7588    5.8772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4255    5.3084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6906    4.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0484    4.0504    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9120    5.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1686    4.7087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2939    4.1076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0568    4.8978    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8959    3.9301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5124    5.2087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0967    3.9178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0323    2.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0312    4.9288    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8341    4.7390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4654    4.3284    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6625    4.5182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9898    6.0316    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7281    3.5072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3606    3.5101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6226    5.4982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2537    3.1867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8996    3.7280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6124    3.6266    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3895    3.1877    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1607    3.8217    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8597    4.7080    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5133    4.7320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5309    3.3174    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4910    4.2974    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7196    3.9761    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338    3.1276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  2  0  0  0  0
 12 11  1  0  0  0  0
 13 10  1  0  0  0  0
 16  1  2  0  0  0  0
 16  2  1  0  0  0  0
 17  3  2  0  0  0  0
 17 14  1  0  0  0  0
 18  8  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 10  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 23 11  1  0  0  0  0
 24 18  2  0  0  0  0
 25 19  1  0  0  0  0
 25 21  1  0  0  0  0
 25 24  1  0  0  0  0
 26 22  2  0  0  0  0
 26 24  1  0  0  0  0
 27 26  1  0  0  0  0
 29 16  1  1  0  0  0
 29 28  1  0  0  0  0
 30 20  1  0  0  0  0
 30 27  1  0  0  0  0
 31 27  2  0  0  0  0
 32 28  1  0  0  0  0
 33  4  1  0  0  0  0
 33  5  1  0  0  0  0
 33 21  1  0  0  0  0
 34  6  1  1  0  0  0
 34 12  1  0  0  0  0
 35  7  1  6  0  0  0
 35 20  1  0  0  0  0
 35 31  1  0  0  0  0
 35 34  1  0  0  0  0
 36 13  1  0  0  0  0
 36 34  1  0  0  0  0
 37 23  1  0  0  0  0
 37 32  1  0  0  0  0
 37 36  1  0  0  0  0
 38 22  1  0  0  0  0
 38 31  1  0  0  0  0
 28 39  1  1  0  0  0
 36 40  1  6  0  0  0
 41 23  1  0  0  0  0
 41 29  1  0  0  0  0
 42 30  1  0  0  0  0
 42 33  1  0  0  0  0
 43 32  1  0  0  0  0
 37 43  1  6  0  0  0
 19 44  1  6  0  0  0
 20 45  1  1  0  0  0
 21 46  1  1  0  0  0
 23 47  1  6  0  0  0
 25 48  1  6  0  0  0
 28 49  1  6  0  0  0
 29 50  1  6  0  0  0
 30 51  1  6  0  0  0
 32 52  1  1  0  0  0
M  END


  Mrv1652305152100352D          

 52 61  0  0  1  0            999 V2000
    2.0169    5.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6881    4.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1587    4.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5703    2.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5674    2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5970    5.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9389    5.5573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1629    6.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3843    6.4151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5053    3.3484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913    5.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7941    5.7190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7025    3.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9782    5.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5544    2.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    5.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3360    4.6701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3161    5.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8711    3.9886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0711    3.9488    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7757    3.2718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7588    5.8772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4255    5.3084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6906    4.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0484    4.0504    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9120    5.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1686    4.7087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2939    4.1076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0568    4.8978    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8959    3.9301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5124    5.2087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0967    3.9178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0323    2.9140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0312    4.9288    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8341    4.7390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4654    4.3284    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6625    4.5182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9898    6.0316    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7281    3.5072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3606    3.5101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6226    5.4982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2537    3.1867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8996    3.7280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6124    3.6266    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3895    3.1877    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1607    3.8217    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8597    4.7080    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5133    4.7320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5309    3.3174    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4910    4.2974    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7196    3.9761    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338    3.1276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  2  0  0  0  0
 12 11  1  0  0  0  0
 13 10  1  0  0  0  0
 16  1  2  0  0  0  0
 16  2  1  0  0  0  0
 17  3  2  0  0  0  0
 17 14  1  0  0  0  0
 18  8  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 10  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 23 11  1  0  0  0  0
 24 18  2  0  0  0  0
 25 19  1  0  0  0  0
 25 21  1  0  0  0  0
 25 24  1  0  0  0  0
 26 22  2  0  0  0  0
 26 24  1  0  0  0  0
 27 26  1  0  0  0  0
 29 16  1  1  0  0  0
 29 28  1  0  0  0  0
 30 20  1  0  0  0  0
 30 27  1  0  0  0  0
 31 27  2  0  0  0  0
 32 28  1  0  0  0  0
 33  4  1  0  0  0  0
 33  5  1  0  0  0  0
 33 21  1  0  0  0  0
 34  6  1  1  0  0  0
 34 12  1  0  0  0  0
 35  7  1  6  0  0  0
 35 20  1  0  0  0  0
 35 31  1  0  0  0  0
 35 34  1  0  0  0  0
 36 13  1  0  0  0  0
 36 34  1  0  0  0  0
 37 23  1  0  0  0  0
 37 32  1  0  0  0  0
 37 36  1  0  0  0  0
 38 22  1  0  0  0  0
 38 31  1  0  0  0  0
 28 39  1  1  0  0  0
 36 40  1  6  0  0  0
 41 23  1  0  0  0  0
 41 29  1  0  0  0  0
 42 30  1  0  0  0  0
 42 33  1  0  0  0  0
 43 32  1  0  0  0  0
 37 43  1  6  0  0  0
 19 44  1  6  0  0  0
 20 45  1  1  0  0  0
 21 46  1  1  0  0  0
 23 47  1  6  0  0  0
 25 48  1  6  0  0  0
 28 49  1  6  0  0  0
 29 50  1  6  0  0  0
 30 51  1  6  0  0  0
 32 52  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0004700

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12O[C@@]11[C@]([H])(CC[C@]3(C)[C@@]4(C)C5=C6C7=C(N5)C=CC5=C7[C@@]7([H])[C@]([H])(C[C@]7([H])C(C)(C)O[C@@]6([H])[C@]4([H])CC[C@@]13O)C(=C)C5)O[C@]([H])(C(C)=C)[C@]2([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C37H45NO5/c1-16(2)29-28(39)32-37(43-32)23(41-29)11-12-34(6)35(7)20(10-13-36(34,37)40)30-27-26-22(38-31(27)35)9-8-18-14-17(3)19-15-21(25(19)24(18)26)33(4,5)42-30/h8-9,19-21,23,25,28-30,32,38-40H,1,3,10-15H2,2,4-7H3/t19-,20+,21+,23+,25+,28+,29-,30+,32-,34-,35-,36+,37+/m1/s1

> <INCHI_KEY>
CRPJNVUYZRFGAK-WKAGVDCZSA-N

> <FORMULA>
C37H45NO5

> <MOLECULAR_WEIGHT>
583.769

> <EXACT_MASS>
583.329773553

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
68.19168547271916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,6S,8R,9S,10R,12S,15R,16S,25S,27S,28S)-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0^{2,16}.0^{5,15}.0^{6,8}.0^{6,12}.0^{17,31}.0^{19,30}.0^{22,29}.0^{25,28}]tritriaconta-17(31),19(30),20,22(29)-tetraene-5,9-diol

> <ALOGPS_LOGP>
5.06

> <JCHEM_LOGP>
4.756595021333334

> <ALOGPS_LOGS>
-6.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
10

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.414904365472658

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.799052627277675

> <JCHEM_PKA_STRONGEST_BASIC>
-3.601193183448812

> <JCHEM_POLAR_SURFACE_AREA>
87.24000000000001

> <JCHEM_REFRACTIVITY>
162.78909999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.66e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,6S,8R,9S,10R,12S,15R,16S,25S,27S,28S)-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0^{2,16}.0^{5,15}.0^{6,8}.0^{6,12}.0^{17,31}.0^{19,30}.0^{22,29}.0^{25,28}]tritriaconta-17(31),19(30),20,22(29)-tetraene-5,9-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       3.765  10.972   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.151   8.376   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      22.696   8.602   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.865   4.272   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.993   4.167   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.314  10.321   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.953  10.374   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.971  11.466   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.517  11.975   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.143   6.250   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.317  11.030   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.816  10.676   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.645   6.605   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.493  10.105   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.701   5.598   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.207   9.497   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.161   8.717   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.257   9.953   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.293   7.445   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.199   7.371   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.248   6.107   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.350  10.971   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.261   9.909   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.089   8.948   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.757   7.561   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.636   9.457   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.248   8.790   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.149   7.668   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.706   9.143   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.739   7.336   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.023   9.723   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.647   7.313   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.860   5.440   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.258   9.200   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.757   8.846   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.202   8.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.703   8.434   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      14.914  11.259   0.000  0.00  0.00           N+0
HETATM   39  O   UNK     0       5.092   6.547   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      10.006   6.552   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       6.762  10.263   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      15.407   5.949   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       9.146   6.959   0.000  0.00  0.00           O+0
HETATM   44  H   UNK     0      21.677   6.770   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      13.794   5.950   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      17.100   7.134   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       7.205   8.788   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0      19.625   8.833   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0       6.591   6.193   0.000  0.00  0.00           H+0
HETATM   50  H   UNK     0       4.650   8.022   0.000  0.00  0.00           H+0
HETATM   51  H   UNK     0      16.277   7.422   0.000  0.00  0.00           H+0
HETATM   52  H   UNK     0       8.090   5.838   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3   17                                                            
CONECT    4   33                                                            
CONECT    5   33                                                            
CONECT    6   34                                                            
CONECT    7   35                                                            
CONECT    8    9   18                                                       
CONECT    9    8   22                                                       
CONECT   10   13   20                                                       
CONECT   11   12   23                                                       
CONECT   12   11   34                                                       
CONECT   13   10   36                                                       
CONECT   14   17   18                                                       
CONECT   15   19   21                                                       
CONECT   16    1    2   29                                                  
CONECT   17    3   14   19                                                  
CONECT   18    8   14   24                                                  
CONECT   19   15   17   25   44                                             
CONECT   20   10   30   35   45                                             
CONECT   21   15   25   33   46                                             
CONECT   22    9   26   38                                                  
CONECT   23   11   37   41   47                                             
CONECT   24   18   25   26                                                  
CONECT   25   19   21   24   48                                             
CONECT   26   22   24   27                                                  
CONECT   27   26   30   31                                                  
CONECT   28   29   32   39   49                                             
CONECT   29   16   28   41   50                                             
CONECT   30   20   27   42   51                                             
CONECT   31   27   35   38                                                  
CONECT   32   28   37   43   52                                             
CONECT   33    4    5   21   42                                             
CONECT   34    6   12   35   36                                             
CONECT   35    7   20   31   34                                             
CONECT   36   13   34   37   40                                             
CONECT   37   23   32   36   43                                             
CONECT   38   22   31                                                       
CONECT   39   28                                                            
CONECT   40   36                                                            
CONECT   41   23   29                                                       
CONECT   42   30   33                                                       
CONECT   43   32   37                                                       
CONECT   44   19                                                            
CONECT   45   20                                                            
CONECT   46   21                                                            
CONECT   47   23                                                            
CONECT   48   25                                                            
CONECT   49   28                                                            
CONECT   50   29                                                            
CONECT   51   30                                                            
CONECT   52   32                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  122    0
END

Synonyms

Value	Source
Tremortin b	MeSH
Penitrem a	MeSH
Penitrem D	MeSH
Tremortin	MeSH
Tremortin a	MeSH
Penitrem e	MeSH
Penitrems	MeSH

Molecular Formula

C₃₇H₄₅NO₅

Average Mass

583.769

Monoisotopic Mass

583.329773553

IUPAC Name

(1S,2R,5S,6S,8R,9S,10R,12S,15R,16S,25S,27S,28S)-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0^{2,16}.0^{5,15}.0^{6,8}.0^{6,12}.0^{17,31}.0^{19,30}.0^{22,29}.0^{25,28}]tritriaconta-17(31),19(30),20,22(29)-tetraene-5,9-diol

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@]12O[C@@]11[C@]([H])(CC[C@]3(C)[C@@]4(C)C5=C6C7=C(N5)C=CC5=C7[C@@]7([H])[C@]([H])(C[C@]7([H])C(C)(C)O[C@@]6([H])[C@]4([H])CC[C@@]13O)C(=C)C5)O[C@]([H])(C(C)=C)[C@]2([H])O

InChI Identifier

InChI=1S/C37H45NO5/c1-16(2)29-28(39)32-37(43-32)23(41-29)11-12-34(6)35(7)20(10-13-36(34,37)40)30-27-26-22(38-31(27)35)9-8-18-14-17(3)19-15-21(25(19)24(18)26)33(4,5)42-30/h8-9,19-21,23,25,28-30,32,38-40H,1,3,10-15H2,2,4-7H3/t19-,20+,21+,23+,25+,28+,29-,30+,32-,34-,35-,36+,37+/m1/s1

InChI Key

CRPJNVUYZRFGAK-WKAGVDCZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Tetralin
3-alkylindole
Indole
Indole or derivatives
1,4-dioxepane
Dioxepane
Monosaccharide
Oxane
Pyran
Benzenoid
Pyrrole
Cyclic alcohol
Tertiary alcohol
Heteroaromatic compound
Secondary alcohol
Azacycle
Oxacycle
Dialkyl ether
Oxirane
Ether
Alcohol
Organopnictogen compound
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00047 g/L	ALOGPS
logP	5.06	ALOGPS
logP	4.76	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	12.8	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	87.24 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	162.79 m³·mol⁻¹	ChemAxon
Polarizability	68.19 Å³	ChemAxon
Number of Rings	10	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	2	Human feces	Metabolic reconstruction

Exposure Sources

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00023568

Chemspider ID

2341202

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3084087

PDB ID

Not Available

ChEBI ID

138831

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Penitrem B (MMDBc0004700)

MOL for #<Metabolite:0x00007fdb2c64cf30>

3D MOL for #<Metabolite:0x00007fdb2c64cf30>

3D SDF for #<Metabolite:0x00007fdb2c64cf30>

3D-SDF for #<Metabolite:0x00007fdb2c64cf30>

PDB for #<Metabolite:0x00007fdb2c64cf30>

3D PDB for #<Metabolite:0x00007fdb2c64cf30>

SMILES for #<Metabolite:0x00007fdb2c64cf30>

INCHI for #<Metabolite:0x00007fdb2c64cf30>

Structure for #<Metabolite:0x00007fdb2c64cf30>

3D Structure for #<Metabolite:0x00007fdb2c64cf30>