MiMeDB: Showing metabocard for Pyripyropene D (MMDBc0001848)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:22:40 UTC

Update Date

2025-10-07 16:04:31 UTC

Metabolite ID

MMDBc0001848

Metabolite Identification

Common Name

Pyripyropene D

Description

Pyripyropene D is a polyketide compound that belongs to the class of natural products known as pyripyropenes, which are characterized by their unique structural features and biological activity. This metabolite has been identified in various studies, indicating its potential role in biological systems, particularly in the context of insect physiology and pest management. Pyripyropene D is noted for its ability to inhibit chitin synthesis, making it a candidate for use in insecticides targeting chitin-dependent organisms. The limited literature on Pyripyropene D suggests that further research is necessary to fully understand its mechanisms of action and potential applications in agriculture and beyond. Notably, studies have indicated its relevance in the context of pest control strategies (PMID: 12627445 ) and its potential interactions with other biological pathways (PMID: 19322173 ). Despite its promise, the current understanding of Pyripyropene D remains somewhat rudimentary, necessitating more comprehensive investigations to elucidate its full biological significance and chemical properties.

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004231521012D          

 43 47  0  0  0  0            999 V2000
   -3.7637    0.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4936   -0.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0337   -0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8439   -0.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7637   -1.7507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8734   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -3.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -3.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -4.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870   -4.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -4.0893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -5.4925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -3.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -3.3098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -0.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -2.3743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773   -1.4389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2575   -2.3743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7976   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6077   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8777   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3377   -3.3098    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5275   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8676   -3.4903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4532   -2.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0953   -2.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8649   -2.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9925   -3.5774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5070   -2.2443    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  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
 15 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  9 25  1  0  0  0  0
 18 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 21 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 11 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END


  Mrv1533004231521012D          

 43 47  0  0  0  0            999 V2000
   -3.7637    0.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4936   -0.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0337   -0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8439   -0.8152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7637   -1.7507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9535   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4135   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3333   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8734   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033   -3.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932   -3.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -4.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2870   -4.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -4.0893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -5.4925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -3.9334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570   -3.3098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8271   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531   -0.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231   -2.3743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0971   -0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1773   -1.4389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9073   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2575   -2.3743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7976   -1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6077   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8777   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3377   -3.3098    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5275   -3.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8676   -3.4903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4532   -2.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0953   -2.4652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8649   -2.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9925   -3.5774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5070   -2.2443    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  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
 15 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  9 25  1  0  0  0  0
 18 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 21 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 11 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001848

> <DATABASE_NAME>
MIME

> <SMILES>
CCC(=O)OC1CCC2(C)C(CC(OC(C)=O)C3(C)OC4=C(C(O)C23)C(=O)OC(=C4)C2=CC=CN=C2)C1(C)COC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H39NO10/c1-7-25(36)42-23-10-11-30(4)22(31(23,5)16-39-17(2)34)14-24(40-18(3)35)32(6)28(30)27(37)26-21(43-32)13-20(41-29(26)38)19-9-8-12-33-15-19/h8-9,12-13,15,22-24,27-28,37H,7,10-11,14,16H2,1-6H3

> <INCHI_KEY>
ORMKQTVTTFTZHC-UHFFFAOYSA-N

> <FORMULA>
C32H39NO10

> <MOLECULAR_WEIGHT>
597.661

> <EXACT_MASS>
597.25739646

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
63.75587576867754

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(acetyloxy)-8-[(acetyloxy)methyl]-12-hydroxy-5a,8,11a-trimethyl-1-oxo-3-(pyridin-3-yl)-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl propanoate

> <ALOGPS_LOGP>
3.55

> <JCHEM_LOGP>
1.6068792529999998

> <ALOGPS_LOGS>
-4.55

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.839017422883682

> <JCHEM_PKA_STRONGEST_BASIC>
4.206336732053717

> <JCHEM_POLAR_SURFACE_AREA>
147.54999999999998

> <JCHEM_REFRACTIVITY>
152.4887

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.67e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(acetyloxy)-8-[(acetyloxy)methyl]-12-hydroxy-5a,8,11a-trimethyl-1-oxo-3-(pyridin-3-yl)-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -7.026   0.807   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.521  -0.649   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.530  -1.813   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -9.042  -1.522   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -7.026  -3.268   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -5.513  -3.559   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.505  -2.395   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.993  -2.686   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.489  -4.141   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.481  -2.977   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.497  -5.305   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.993  -6.760   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.481  -7.051   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.977  -8.507   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.536  -8.798   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.544  -7.633   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.040 -10.253   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.472  -5.887   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.032  -7.342   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.040  -6.178   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.048  -5.014   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.544  -3.559   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.032  -3.268   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.472  -1.813   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.977  -4.432   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.552  -2.395   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.048  -0.940   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.064  -2.686   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.568  -4.141   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.560  -5.305   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.081  -4.432   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.089  -3.268   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.601  -3.559   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.105  -5.014   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0       8.097  -6.178   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0       6.585  -5.887   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -5.009  -5.014   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -5.353  -6.515   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -6.446  -5.569   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -7.644  -4.602   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -9.081  -5.156   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -9.319  -6.678   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -10.280  -4.189   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   25                                             
CONECT   10    9                                                            
CONECT   11    9   12   37                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23   26                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    9   18                                                  
CONECT   26   22   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29   21                                                       
CONECT   31   29   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   11    6   38   39                                             
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

Synonyms

Value	Source
6-(Acetyloxy)-8-[(acetyloxy)methyl]-12-hydroxy-5a,8,11a-trimethyl-1-oxo-3-(pyridin-3-yl)-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl propanoic acid	Generator

Molecular Formula

C₃₂H₃₉NO₁₀

Average Mass

597.661

Monoisotopic Mass

597.25739646

IUPAC Name

6-(acetyloxy)-8-[(acetyloxy)methyl]-12-hydroxy-5a,8,11a-trimethyl-1-oxo-3-(pyridin-3-yl)-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphen-9-yl propanoate

Traditional Name

6-(acetyloxy)-8-[(acetyloxy)methyl]-12-hydroxy-5a,8,11a-trimethyl-1-oxo-3-(pyridin-3-yl)-6,7,7a,9,10,11,11b,12-octahydro-2,5-dioxatetraphen-9-yl propanoate

CAS Registry Number

Not Available

SMILES

CCC(=O)OC1CCC2(C)C(CC(OC(C)=O)C3(C)OC4=C(C(O)C23)C(=O)OC(=C4)C2=CC=CN=C2)C1(C)COC(C)=O

InChI Identifier

InChI=1S/C32H39NO10/c1-7-25(36)42-23-10-11-30(4)22(31(23,5)16-39-17(2)34)14-24(40-18(3)35)32(6)28(30)27(37)26-21(43-32)13-20(41-29(26)38)19-9-8-12-33-15-19/h8-9,12-13,15,22-24,27-28,37H,7,10-11,14,16H2,1-6H3

InChI Key

ORMKQTVTTFTZHC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxysteroids. These are steroids carrying a hydroxyl group at the 1-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

1-hydroxysteroids

Alternative Parents

Substituents

1-hydroxysteroid
Naphthopyran
Naphthalene
Tricarboxylic acid or derivatives
Alkyl aryl ether
Pyranone
Pyran
Pyridine
Heteroaromatic compound
Vinylogous ester
Secondary alcohol
Carboxylic acid ester
Lactone
Azacycle
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Ether
Organic nitrogen compound
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
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	0.017 g/L	ALOGPS
logP	3.55	ALOGPS
logP	1.61	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	13.84	ChemAxon
pKa (Strongest Basic)	4.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	147.55 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	152.49 m³·mol⁻¹	ChemAxon
Polarizability	63.76 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum

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

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

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	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10326201

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Pyripyropene D (MMDBc0001848)

MOL for #<Metabolite:0x00007fb4e88b1240>

3D MOL for #<Metabolite:0x00007fb4e88b1240>

3D SDF for #<Metabolite:0x00007fb4e88b1240>

3D-SDF for #<Metabolite:0x00007fb4e88b1240>

PDB for #<Metabolite:0x00007fb4e88b1240>

3D PDB for #<Metabolite:0x00007fb4e88b1240>

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Structure for #<Metabolite:0x00007fb4e88b1240>

3D Structure for #<Metabolite:0x00007fb4e88b1240>