NP-MRD: Showing NP-Card for Phomoeuphorbin C (NP0007995)

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Record Information

Version

2.0

Created at

2020-12-09 05:36:27 UTC

Updated at

2021-07-15 16:59:08 UTC

NP-MRD ID

NP0007995

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Phomoeuphorbin C

Provided By

NPAtlas

Description

Phomoeuphorbin C belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. Phomoeuphorbin C is found in Phomopsis euphorbiae. Based on a literature review very few articles have been published on Phomoeuphorbin C.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106063D          

 41 42  0  0  0  0            999 V2000
    4.8206    2.0221    0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4044    0.5857    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    0.0654   -0.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1147   -1.3826   -0.0347 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2690   -2.0483    0.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298   -1.4590    1.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7894   -2.7591    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601   -0.6939    0.8355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0571   -1.3989   -0.1233 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2618   -0.5230   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.0654   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.2445   -1.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7617   -0.9932   -0.9652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6145    0.9355   -0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8174    1.8138   -0.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6753    0.4355    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    1.7065   -0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2596    2.8913   -0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    0.9100   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010    1.4661    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6526    0.4736 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7408    2.5303    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    2.0550    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2156    2.5727   -0.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9116   -0.0093    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9733    0.6703   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7745   -1.8258   -0.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2498   -3.0059    0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6099   -0.9975    1.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5833   -3.3273    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -0.6478    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4068   -2.3370    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -1.5992   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3834   -2.1504   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4449    0.1847   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0727   -1.1291   -1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072    2.8888   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204    1.4926    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2351    1.7099   -1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9251   -0.5352    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0094    2.5434    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  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
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  1  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21  8  1  0  0  0  0
 19 10  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  2 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  6  0  0  0
  5 28  1  0  0  0  0
  6 29  1  1  0  0  0
  7 30  1  0  0  0  0
  8 31  1  1  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
 11 34  1  0  0  0  0
 12 35  1  6  0  0  0
 13 36  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
 16 40  1  0  0  0  0
 20 41  1  0  0  0  0
M  END

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
    4.8206    2.0221    0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4044    0.5857    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    0.0654   -0.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1147   -1.3826   -0.0347 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2690   -2.0483    0.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298   -1.4590    1.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7894   -2.7591    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601   -0.6939    0.8355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0571   -1.3989   -0.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618   -0.5230   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.0654   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.2445   -1.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7617   -0.9932   -0.9652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6145    0.9355   -0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8174    1.8138   -0.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6753    0.4355    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    1.7065   -0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2596    2.8913   -0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    0.9100   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010    1.4661    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6526    0.4736 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7408    2.5303    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    2.0550    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2156    2.5727   -0.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9116   -0.0093    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9733    0.6703   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7745   -1.8258   -0.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2498   -3.0059    0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6099   -0.9975    1.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5833   -3.3273    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -0.6478    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4068   -2.3370    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -1.5992   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3834   -2.1504   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4449    0.1847   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0727   -1.1291   -1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072    2.8888   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204    1.4926    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2351    1.7099   -1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9251   -0.5352    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0094    2.5434    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  1
 14 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21  8  1  0
 19 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  6 29  1  1
  7 30  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
 11 34  1  0
 12 35  1  6
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 20 41  1  0
M  END


  Mrv1652306242106063D          

 41 42  0  0  0  0            999 V2000
    4.8206    2.0221    0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4044    0.5857    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    0.0654   -0.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1147   -1.3826   -0.0347 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2690   -2.0483    0.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298   -1.4590    1.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7894   -2.7591    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601   -0.6939    0.8355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0571   -1.3989   -0.1233 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2618   -0.5230   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.0654   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.2445   -1.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7617   -0.9932   -0.9652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6145    0.9355   -0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8174    1.8138   -0.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6753    0.4355    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    1.7065   -0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2596    2.8913   -0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    0.9100   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010    1.4661    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6526    0.4736 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7408    2.5303    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    2.0550    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2156    2.5727   -0.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9116   -0.0093    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9733    0.6703   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7745   -1.8258   -0.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2498   -3.0059    0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6099   -0.9975    1.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5833   -3.3273    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -0.6478    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4068   -2.3370    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -1.5992   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3834   -2.1504   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4449    0.1847   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0727   -1.1291   -1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072    2.8888   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204    1.4926    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2351    1.7099   -1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9251   -0.5352    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0094    2.5434    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  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
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  1  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21  8  1  0  0  0  0
 19 10  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  2 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  6  0  0  0
  5 28  1  0  0  0  0
  6 29  1  1  0  0  0
  7 30  1  0  0  0  0
  8 31  1  1  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
 11 34  1  0  0  0  0
 12 35  1  6  0  0  0
 13 36  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
 16 40  1  0  0  0  0
 20 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007995

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]([H])(C(\[H])=C(/[H])C([H])([H])[H])[C@]([H])(O[H])[C@@]1([H])OC([H])=C2C(=O)[C@@](O[H])(C([H])([H])[H])[C@]([H])(O[H])C([H])=C2C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O6/c1-3-4-10(16)13(18)11-5-8-6-12(17)15(2,20)14(19)9(8)7-21-11/h3-4,6-7,10-13,16-18,20H,5H2,1-2H3/b4-3+/t10-,11+,12-,13+,15-/m1/s1

> <INCHI_KEY>
GMZCDOTXVJKLNB-TVIYMLLGSA-N

> <FORMULA>
C15H20O6

> <MOLECULAR_WEIGHT>
296.319

> <EXACT_MASS>
296.125988364

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
30.39462384640325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6R,7R)-3-[(1S,2R,3E)-1,2-dihydroxypent-3-en-1-yl]-6,7-dihydroxy-7-methyl-4,6,7,8-tetrahydro-3H-2-benzopyran-8-one

> <ALOGPS_LOGP>
-0.10

> <JCHEM_LOGP>
-0.5704906133333332

> <ALOGPS_LOGS>
-1.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.076020380024637

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.14752087069004

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3408254260796193

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
76.86559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6R,7R)-3-[(1S,2R,3E)-1,2-dihydroxypent-3-en-1-yl]-6,7-dihydroxy-7-methyl-4,6-dihydro-3H-2-benzopyran-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
    4.8206    2.0221    0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4044    0.5857    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    0.0654   -0.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1147   -1.3826   -0.0347 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2690   -2.0483    0.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298   -1.4590    1.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7894   -2.7591    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601   -0.6939    0.8355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0571   -1.3989   -0.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618   -0.5230   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.0654   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.2445   -1.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7617   -0.9932   -0.9652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6145    0.9355   -0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8174    1.8138   -0.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6753    0.4355    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    1.7065   -0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2596    2.8913   -0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    0.9100   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010    1.4661    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6526    0.4736 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7408    2.5303    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    2.0550    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2156    2.5727   -0.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9116   -0.0093    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9733    0.6703   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7745   -1.8258   -0.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2498   -3.0059    0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6099   -0.9975    1.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5833   -3.3273    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -0.6478    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4068   -2.3370    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -1.5992   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3834   -2.1504   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4449    0.1847   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0727   -1.1291   -1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072    2.8888   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204    1.4926    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2351    1.7099   -1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9251   -0.5352    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0094    2.5434    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  1
 14 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21  8  1  0
 19 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  6 29  1  1
  7 30  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
 11 34  1  0
 12 35  1  6
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 20 41  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       4.821   2.022   0.472  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.404   0.586   0.577  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.466   0.065  -0.212  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.115  -1.383  -0.035  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.269  -2.048   0.362  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.130  -1.459   1.095  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.789  -2.759   1.440  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.860  -0.694   0.836  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.057  -1.399  -0.123  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.262  -0.523  -0.367  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.390  -1.065  -0.775  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.583  -0.245  -1.027  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.762  -0.993  -0.965  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.615   0.936  -0.101  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.817   1.814  -0.321  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.675   0.436   1.204  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.352   1.706  -0.313  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.260   2.891  -0.635  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.125   0.910  -0.097  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.001   1.466   0.301  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.111   0.653   0.474  0.00  0.00           O+0
HETATM   22  H   UNK     0       4.741   2.530   1.458  0.00  0.00           H+0
HETATM   23  H   UNK     0       5.878   2.055   0.167  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.216   2.573  -0.260  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.912  -0.009   1.334  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.973   0.670  -0.958  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.775  -1.826  -0.970  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.250  -3.006   0.114  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.610  -0.998   1.986  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.583  -3.327   0.660  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.319  -0.648   1.817  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.407  -2.337   0.316  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.380  -1.599  -1.101  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.383  -2.150  -0.913  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.445   0.185  -2.058  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.073  -1.129  -1.894  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.607   2.889  -0.068  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.620   1.493   0.374  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.235   1.710  -1.346  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.925  -0.535   1.212  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.009   2.543   0.472  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   25                                                  
CONECT    3    2    4   26                                                  
CONECT    4    3    5    6   27                                             
CONECT    5    4   28                                                       
CONECT    6    4    7    8   29                                             
CONECT    7    6   30                                                       
CONECT    8    6    9   21   31                                             
CONECT    9    8   10   32   33                                             
CONECT   10    9   11   19                                                  
CONECT   11   10   12   34                                                  
CONECT   12   11   13   14   35                                             
CONECT   13   12   36                                                       
CONECT   14   12   15   16   17                                             
CONECT   15   14   37   38   39                                             
CONECT   16   14   40                                                       
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   10                                                  
CONECT   20   19   21   41                                                  
CONECT   21   20    8                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    3                                                            
CONECT   27    4                                                            
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    7                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   11                                                            
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   20                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

RDKit          3D

41 42  0  0  0  0  0  0  0  0999 V2000
    4.8206    2.0221    0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4044    0.5857    0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    0.0654   -0.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1147   -1.3826   -0.0347 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2690   -2.0483    0.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298   -1.4590    1.0947 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7894   -2.7591    1.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8601   -0.6939    0.8355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0571   -1.3989   -0.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618   -0.5230   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.0654   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5827   -0.2445   -1.0272 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7617   -0.9932   -0.9652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6145    0.9355   -0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8174    1.8138   -0.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6753    0.4355    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    1.7065   -0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2596    2.8913   -0.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    0.9100   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0010    1.4661    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105    0.6526    0.4736 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7408    2.5303    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8782    2.0550    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2156    2.5727   -0.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9116   -0.0093    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9733    0.6703   -0.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7745   -1.8258   -0.9699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2498   -3.0059    0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6099   -0.9975    1.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5833   -3.3273    0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -0.6478    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4068   -2.3370    0.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -1.5992   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3834   -2.1504   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4449    0.1847   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0727   -1.1291   -1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072    2.8888   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204    1.4926    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2351    1.7099   -1.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9251   -0.5352    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0094    2.5434    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  1
 14 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21  8  1  0
 19 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  6 29  1  1
  7 30  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
 11 34  1  0
 12 35  1  6
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 20 41  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₆

Average Mass

296.3190 Da

Monoisotopic Mass

296.12599 Da

IUPAC Name

(3S,6R,7R)-3-[(1S,2R,3E)-1,2-dihydroxypent-3-en-1-yl]-6,7-dihydroxy-7-methyl-4,6,7,8-tetrahydro-3H-2-benzopyran-8-one

Traditional Name

(3S,6R,7R)-3-[(1S,2R,3E)-1,2-dihydroxypent-3-en-1-yl]-6,7-dihydroxy-7-methyl-4,6-dihydro-3H-2-benzopyran-8-one

CAS Registry Number

Not Available

SMILES

C\C=C\C(O)C(O)[C@@H]1CC2=C[C@@H](O)[C@@](C)(O)C(=O)C2=CO1

InChI Identifier

InChI=1S/C15H20O6/c1-3-4-10(16)13(18)11-5-8-6-12(17)15(2,20)14(19)9(8)7-21-11/h3-4,6-7,10-13,16-18,20H,5H2,1-2H3/b4-3+/t10?,11-,12+,13?,15+/m0/s1

InChI Key

GMZCDOTXVJKLNB-TVIYMLLGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Phomopsis euphorbiae	NPAtlas	18799173

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

Not Available

Direct Parent

Benzopyrans

Alternative Parents

Substituents

Benzopyran
Cyclohexenone
Acyloin
Vinylogous ester
Tertiary alcohol
Secondary alcohol
Ketone
Oxacycle
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
logP	-0.1	ALOGPS
logP	-0.57	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	76.87 m³·mol⁻¹	ChemAxon
Polarizability	30.39 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA012385

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00034136

Chemspider ID

78441220

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25113769

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Phomoeuphorbin C (NP0007995)

MOL for NP0007995 (Phomoeuphorbin C)

3D MOL for NP0007995 (Phomoeuphorbin C)

3D SDF for NP0007995 (Phomoeuphorbin C)

3D-SDF for NP0007995 (Phomoeuphorbin C)

PDB for NP0007995 (Phomoeuphorbin C)

3D PDB for NP0007995 (Phomoeuphorbin C)

SMILES for NP0007995 (Phomoeuphorbin C)

INCHI for NP0007995 (Phomoeuphorbin C)

Structure for NP0007995 (Phomoeuphorbin C)

3D Structure for NP0007995 (Phomoeuphorbin C)