NP-MRD: Showing NP-Card for (2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid (NP0243050)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 03:31:01 UTC

Updated at

2022-09-07 03:31:01 UTC

NP-MRD ID

NP0243050

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid

Description

Neoabyssomicin C belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. (2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid is found in Streptomyces koyangensis. Based on a literature review very few articles have been published on Neoabyssomicin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072205312D          

 27 29  0  0  1  0            999 V2000
   -2.1056    2.8634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7923    2.1002    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2967    1.4473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9748    1.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6615    1.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1561    1.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6604    1.7692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693    0.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3116    0.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9832    0.7963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8905    0.5243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5130    1.0656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2363    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5256    0.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1586   -0.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4509   -0.7564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6248   -0.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0276   -0.3626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7919   -0.4575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3818   -1.0252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5922   -1.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0065   -2.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2168   -3.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0129   -3.4184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6312   -3.7828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0268   -0.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8122   -0.6178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 20 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    5.4740    1.8290   -0.9205 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6864    0.5466   -0.1688 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7749   -0.1744   -0.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4339   -0.3048   -0.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2608    0.4571    0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0269   -0.3427    0.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1269   -1.4818   -0.5117 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7251    0.1458    0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3923   -0.5131    0.3646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8483   -1.7333   -0.1262 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2562   -1.9450    0.1037 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7236   -3.2509   -0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5748   -1.7914    1.5717 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9583   -2.9139    2.3978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0882   -0.4682    2.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4700    0.3459    0.9461 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8487    1.5104    1.3867 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5188    1.4407    1.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3451    2.3230    1.3936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5371    0.5501   -0.0920 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1097    1.3923   -1.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6850    2.5375   -1.5324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    3.3509   -2.6546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    2.9813   -3.3688 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8420    4.5529   -2.9859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9506   -0.8068   -0.6181 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3368   -0.9891   -0.5653 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9444    1.6857   -1.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4721    2.2999   -1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8893    2.5097   -0.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8088    0.7831    0.9169 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2446    0.3080   -1.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6102   -1.2534    0.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2859   -0.4900   -1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3779    0.6135    1.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1568    1.4305   -0.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5323   -4.0349    0.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1479   -3.5764   -1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017   -3.1956   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6826   -1.7983    1.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0041   -3.1864    1.8656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6930   -2.5573    3.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6778   -3.7523    2.4187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8882    0.1016    2.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2834   -0.6299    2.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4363    0.9603    0.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2805    1.0815   -1.8325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    2.9082   -0.9569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7337    4.7670   -2.5221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6554   -0.9028   -1.6973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6988   -1.3202   -1.4381 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  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  1
 17 18  1  0
 18 19  2  0
 16 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 25  1  0
 23 24  2  0
 20 26  1  0
 26 27  1  0
 18  8  1  0
 16  9  1  0
 26 11  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  6
 14 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 20 46  1  1
 21 47  1  0
 22 48  1  0
 25 49  1  0
 26 50  1  6
 27 51  1  0
M  END


  Mrv1652309072205312D          

 27 29  0  0  1  0            999 V2000
   -2.1056    2.8634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7923    2.1002    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2967    1.4473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9748    1.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6615    1.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1561    1.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6604    1.7692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693    0.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3116    0.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9832    0.7963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8905    0.5243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5130    1.0656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2363    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5256    0.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1586   -0.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4509   -0.7564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6248   -0.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0276   -0.3626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7919   -0.4575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3818   -1.0252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5922   -1.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0065   -2.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2168   -3.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0129   -3.4184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6312   -3.7828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0268   -0.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8122   -0.6178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
 16 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 20 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0243050

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)CCC(=O)C1=C2O[C@@]3(C)[C@@H](C)C[C@]2(OC1=O)[C@@H](\C=C\C(O)=O)[C@@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O8/c1-9-8-19-11(5-7-13(22)23)15(24)18(9,3)26-16(19)14(17(25)27-19)12(21)6-4-10(2)20/h5,7,9-11,15,20,24H,4,6,8H2,1-3H3,(H,22,23)/b7-5+/t9-,10-,11-,15-,18-,19-/m0/s1

> <INCHI_KEY>
HXUORWAUCSCXSP-NFUGBNBJSA-N

> <FORMULA>
C19H24O8

> <MOLECULAR_WEIGHT>
380.393

> <EXACT_MASS>
380.147117733

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
38.09803751901293

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-[(1S,7S,8S,9S,11S)-8-hydroxy-4-[(4S)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0^{1,5}]undec-4-en-9-yl]prop-2-enoic acid

> <JCHEM_LOGP>
0.41925789266666674

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.597308409353868

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.128007631023911

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5157976660585213

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
94.20849999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-[(1S,7S,8S,9S,11S)-8-hydroxy-4-[(4S)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0^{1,5}]undec-4-en-9-yl]prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.930   5.345   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.346   3.920   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.287   2.702   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.820   3.714   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.235   2.290   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.291   2.084   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.233   3.302   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.876   0.659   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.448   0.276   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.702   1.486   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.396   0.979   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.558   1.989   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.105   0.441   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.848   1.330   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.029  -0.952   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.708  -1.412   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.166  -1.796   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.052  -0.677   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.478  -0.854   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.446  -1.914   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.839  -3.403   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.745  -4.487   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.138  -5.977   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.624  -6.381   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.045  -7.061   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.650  -0.682   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.116  -1.153   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   18                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   26                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    9   17   20                                             
CONECT   17   16   18                                                       
CONECT   18   17    8   19                                                  
CONECT   19   18                                                            
CONECT   20   16   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   20   11   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄O₈

Average Mass

380.3930 Da

Monoisotopic Mass

380.14712 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](O)CCC(=O)C1=C2O[C@@]3(C)[C@@H](C)C[C@]2(OC1=O)[C@@H](\C=C\C(O)=O)[C@@H]3O

InChI Identifier

InChI=1S/C19H24O8/c1-9-8-19-11(5-7-13(22)23)15(24)18(9,3)26-16(19)14(17(25)27-19)12(21)6-4-10(2)20/h5,7,9-11,15,20,24H,4,6,8H2,1-3H3,(H,22,23)/b7-5+/t9-,10-,11-,15-,18-,19-/m0/s1

InChI Key

HXUORWAUCSCXSP-NFUGBNBJSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Streptomyces koyangensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Oxane
Dicarboxylic acid or derivatives
2-furanone
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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

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

78439176

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590207

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid (NP0243050)

MOL for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

3D MOL for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

3D SDF for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

3D-SDF for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

PDB for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

3D PDB for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

SMILES for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

INCHI for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

Structure for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)

3D Structure for NP0243050 ((2e)-3-[(1s,7s,8s,9s,11s)-8-hydroxy-4-[(4s)-4-hydroxypentanoyl]-7,11-dimethyl-3-oxo-2,6-dioxatricyclo[5.2.2.0¹,⁵]undec-4-en-9-yl]prop-2-enoic acid)