NP-MRD: Showing NP-Card for 15-One-12β,25,28-trihydroxy-ergone (NP0332642)

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Record Information

Version

2.0

Created at

2024-03-15 14:23:22 UTC

Updated at

2024-11-01 01:36:11 UTC

NP-MRD ID

NP0332642

Natural Product DOI

https://doi.org/10.57994/1902

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-One-12β,25,28-trihydroxy-ergone

Description

15-One-12β,25,28-trihydroxy-ergone belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, 15-one-12β,25,28-trihydroxy-ergone is considered to be a sterol. Based on a literature review very few articles have been published on 15-One-12β,25,28-trihydroxy-ergone.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 03152414232D          

 35 38  0  0  1  0            999 V2000
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7411   -1.2236    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1264   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5781   -2.4560    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0845   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9017   -2.9945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8890   -1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1999   -0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6532   -2.0027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1248   -1.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4506    0.7010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8548   -2.8125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2018   -0.3395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 12 27  2  0  0  0  0
 28 11  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 33 32  1  0  0  0  0
 33 10  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  1  0  0  0
  7 35  2  0  0  0  0
  2 35  1  0  0  0  0
M  END


  Mrv2104 03152414232D          

 35 38  0  0  1  0            999 V2000
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7411   -1.2236    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1264   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5781   -2.4560    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0845   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9017   -2.9945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8890   -1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1999   -0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6532   -2.0027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1248   -1.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4506    0.7010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8548   -2.8125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2018   -0.3395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 12 27  2  0  0  0  0
 28 11  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 33 32  1  0  0  0  0
 33 10  1  0  0  0  0
  5 33  1  0  0  0  0
 33 34  1  1  0  0  0
  7 35  2  0  0  0  0
  2 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332642

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]1(CC(=O)C2=C3C=CC4=CC(=O)CC[C@]4(C)[C@@]3([H])C[C@@H](O)[C@]12C)[C@H](C)\C=C\[C@H](CO)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C28H38O5/c1-16(6-7-18(15-29)26(2,3)33)21-13-23(31)25-20-9-8-17-12-19(30)10-11-27(17,4)22(20)14-24(32)28(21,25)5/h6-9,12,16,18,21-22,24,29,32-33H,10-11,13-15H2,1-5H3/b7-6+/t16-,18-,21-,22+,24-,27+,28+/m1/s1

> <INCHI_KEY>
XKTKUEKGBQVLAL-VWIKFUJUSA-N

> <FORMULA>
C28H38O5

> <MOLECULAR_WEIGHT>
454.607

> <EXACT_MASS>
454.271924324

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
51.36822462091585

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,9aR,9bR,11R,11aR)-11-hydroxy-1-[(2R,3E,5R)-6-hydroxy-5-(hydroxymethyl)-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,3H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene-3,7-dione

> <JCHEM_LOGP>
2.1076961826666656

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.965950425436118

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.385019448098644

> <JCHEM_PKA_STRONGEST_BASIC>
-2.648277935338597

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
132.728

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,9aR,9bR,11R,11aR)-11-hydroxy-1-[(2R,3E,5R)-6-hydroxy-5-(hydroxymethyl)-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,8H,9H,9bH,10H,11H-cyclopenta[a]phenanthrene-3,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAR-24   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAR-24         0                                  
HETATM    1  O   UNK     0       2.303  -0.998   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.366  -1.095   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   15  H   UNK     0      14.450  -2.284   0.000  0.00  0.00           H+0
HETATM   16  C   UNK     0      13.883  -3.790   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.303  -5.217   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.408  -3.579   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.354  -4.795   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.879  -4.585   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.824  -5.800   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      20.350  -5.590   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      18.459  -3.158   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.040  -1.732   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      19.886  -3.738   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      17.033  -2.578   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.041   1.308   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.070  -4.010   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.929  -5.250   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
HETATM   34  H   UNK     0       7.843  -0.634   0.000  0.00  0.00           H+0
HETATM   35  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   33                                             
CONECT    6    5                                                            
CONECT    7    5    8   35                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   33                                                  
CONECT   11   10   12   28                                                  
CONECT   12   11   13   27                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16   28                                             
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23                                                            
CONECT   27   12                                                            
CONECT   28   11   14   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   10    5   34                                             
CONECT   34   33                                                            
CONECT   35    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₈O₅

Average Mass

454.6070 Da

Monoisotopic Mass

454.27192 Da

IUPAC Name

(1R,9aR,9bR,11R,11aR)-11-hydroxy-1-[(2R,3E,5R)-6-hydroxy-5-(hydroxymethyl)-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,3H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene-3,7-dione

Traditional Name

(1R,9aR,9bR,11R,11aR)-11-hydroxy-1-[(2R,3E,5R)-6-hydroxy-5-(hydroxymethyl)-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,8H,9H,9bH,10H,11H-cyclopenta[a]phenanthrene-3,7-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]1(CC(=O)C2=C3C=CC4=CC(=O)CC[C@]4(C)[C@@]3([H])C[C@@H](O)[C@]12C)[C@H](C)\C=C\[C@H](CO)C(C)(C)O

InChI Identifier

InChI=1S/C28H38O5/c1-16(6-7-18(15-29)26(2,3)33)21-13-23(31)25-20-9-8-17-12-19(30)10-11-27(17,4)22(20)14-24(32)28(21,25)5/h6-9,12,16,18,21-22,24,29,32-33H,10-11,13-15H2,1-5H3/b7-6+/t16-,18-,21-,22+,24-,27+,28+/m1/s1

InChI Key

XKTKUEKGBQVLAL-VWIKFUJUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum
1D_ NMR	¹H NMR Spectrum (1D, 400 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum
1D_ NMR	¹³C NMR Spectrum (1D, 101 MHz, CD3OD, experimental)	[email protected]	Hainan University	zhongbin cheng	2024-03-15	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aspergillus terreus		Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Triterpenoid
Ergosterol-skeleton
25-hydroxysteroid
12-beta-hydroxysteroid
Oxosteroid
15-oxosteroid
Hydroxysteroid
12-hydroxysteroid
3-oxosteroid
Fatty alcohol
Cyclohexenone
Fatty acyl
Alpha-branched alpha,beta-unsaturated-ketone
Alpha,beta-unsaturated ketone
Tertiary alcohol
Enone
Acryloyl-group
Cyclic ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.11	ChemAxon
pKa (Strongest Acidic)	14.39	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	132.73 m³·mol⁻¹	ChemAxon
Polarizability	51.37 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 15-One-12β,25,28-trihydroxy-ergone (NP0332642)

MOL for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

3D MOL for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

3D SDF for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

3D-SDF for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

PDB for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

3D PDB for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

SMILES for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

INCHI for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

Structure for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)

3D Structure for NP0332642 (15-One-12β,25,28-trihydroxy-ergone)