NP-MRD: Showing NP-Card for (1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione (NP0219014)

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Record Information

Version

2.0

Created at

2022-09-05 19:52:04 UTC

Updated at

2022-09-05 19:52:05 UTC

NP-MRD ID

NP0219014

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione

Description

Flavoskyrin belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. (1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione is found in Talaromyces islandicus. (1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione was first documented in 2005 (PMID: 16123947). Based on a literature review a small amount of articles have been published on Flavoskyrin (PMID: 29266494) (PMID: 16095306).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052221522D          

 40 46  0  0  1  0            999 V2000
    6.3101    0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9404    0.9125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3942    1.6014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0245    2.3390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4783    3.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2009    2.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7471    1.6986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1168    0.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1852    2.3434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4285    3.1317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3608    2.6660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5999    1.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0357    1.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    1.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6681    0.8604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9072    0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429   -0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7105   -0.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9496   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854   -1.5084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7530   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3172   -0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1206   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0781    0.2973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2748    0.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8647    1.0481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3004    0.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256    1.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1898    2.4396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9507    3.2292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9932    2.2519    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5574    2.8537    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3183    3.6433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5150    3.8310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8826    4.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    4.0575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2502    4.6594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9250    3.2679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7979    3.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2715    3.8183    0.0000 O   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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 13 25  2  0  0  0  0
 18 25  1  0  0  0  0
 15 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  1  1  0  0  0
 29 31  1  0  0  0  0
 31 14  1  1  0  0  0
 32 31  1  6  0  0  0
 11 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  2  0  0  0  0
  6 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END


  Mrv1652309052221522D          

 40 46  0  0  1  0            999 V2000
    6.3101    0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9404    0.9125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3942    1.6014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0245    2.3390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4783    3.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2009    2.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7471    1.6986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1168    0.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1852    2.3434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4285    3.1317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3608    2.6660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5999    1.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0357    1.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    1.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6681    0.8604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9072    0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429   -0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7105   -0.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9496   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854   -1.5084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7530   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3172   -0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1206   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0781    0.2973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2748    0.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8647    1.0481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3004    0.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256    1.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1898    2.4396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9507    3.2292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9932    2.2519    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5574    2.8537    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3183    3.6433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5150    3.8310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8826    4.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6859    4.0575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2502    4.6594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9250    3.2679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7979    3.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2715    3.8183    0.0000 O   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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 13 25  2  0  0  0  0
 18 25  1  0  0  0  0
 15 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  1  1  0  0  0
 29 31  1  0  0  0  0
 31 14  1  1  0  0  0
 32 31  1  6  0  0  0
 11 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  2  0  0  0  0
  6 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219014

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C3O[C@]45[C@@H]([C@H](O)CC(=O)C4=C(O)C4=C(O)C=C(C)C=C4C5=O)[C@@H]4[C@H](O)CC(=O)C(C(O)=C2C(O)=C1)=C34

> <INCHI_IDENTIFIER>
InChI=1S/C30H24O10/c1-9-3-11-19(13(31)5-9)26(37)22-16(34)7-15(33)21-23(22)28(11)40-30-24(21)17(35)8-18(36)25(30)27(38)20-12(29(30)39)4-10(2)6-14(20)32/h3-6,15,17,21,24,31-33,35,37-38H,7-8H2,1-2H3/t15-,17-,21-,24+,30-/m1/s1

> <INCHI_KEY>
FGOBSKJMUFAKJO-ULLJINMFSA-N

> <FORMULA>
C30H24O10

> <MOLECULAR_WEIGHT>
544.512

> <EXACT_MASS>
544.136946973

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
53.84824526031466

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3R,15R,28R)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0^{2,15}.0^{6,15}.0^{8,13}.0^{18,23}.0^{25,29}]nonacosa-6,8,10,12,17,19,21,23,25(29)-nonaene-5,14,26-trione

> <JCHEM_LOGP>
2.400077660333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.1945052390075

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.210493685272858

> <JCHEM_PKA_STRONGEST_BASIC>
-2.969188078760384

> <JCHEM_POLAR_SURFACE_AREA>
181.82

> <JCHEM_REFRACTIVITY>
141.5602

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3R,15R,28R)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0^{2,15}.0^{6,15}.0^{8,13}.0^{18,23}.0^{25,29}]nonacosa-6,8,10,12,17,19,21,23,25(29)-nonaene-5,14,26-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      11.779   0.327   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.089   1.703   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.936   2.989   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.246   4.366   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.093   5.652   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.708   4.457   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.861   3.171   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.551   1.794   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.812   4.374   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.267   5.846   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.273   4.977   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.720   3.503   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.667   2.379   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.167   2.730   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.114   1.606   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.560   0.132   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.507  -0.991   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.060  -0.218   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.506  -1.692   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.453  -2.816   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.006  -2.043   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.059  -0.919   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.558  -1.269   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.613   0.555   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.113   0.905   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.614   1.957   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.561   0.833   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.168   3.430   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.221   4.554   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.775   6.028   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.721   4.203   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.774   5.327   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.328   6.801   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.828   7.151   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.381   7.924   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.880   7.574   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.934   8.697   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       7.327   6.100   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.956   5.867   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.840   7.128   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   39                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   32   38                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   25                                                  
CONECT   14   13   15   31                                                  
CONECT   15   14   16   26                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   25                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   13   18                                                  
CONECT   26   15   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   14   32                                                  
CONECT   32   31   11   33                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   11   39                                                  
CONECT   39   38    6   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₂₄O₁₀

Average Mass

544.5120 Da

Monoisotopic Mass

544.13695 Da

IUPAC Name

(1S,2R,3R,15R,28R)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0^{2,15}.0^{6,15}.0^{8,13}.0^{18,23}.0^{25,29}]nonacosa-6,8,10,12,17,19,21,23,25(29)-nonaene-5,14,26-trione

Traditional Name

(1S,2R,3R,15R,28R)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0^{2,15}.0^{6,15}.0^{8,13}.0^{18,23}.0^{25,29}]nonacosa-6,8,10,12,17,19,21,23,25(29)-nonaene-5,14,26-trione

CAS Registry Number

Not Available

SMILES

CC1=CC2=C3O[C@]45[C@@H]([C@H](O)CC(=O)C4=C(O)C4=C(O)C=C(C)C=C4C5=O)[C@@H]4[C@H](O)CC(=O)C(C(O)=C2C(O)=C1)=C34

InChI Identifier

InChI=1S/C30H24O10/c1-9-3-11-19(13(31)5-9)26(37)22-16(34)7-15(33)21-23(22)28(11)40-30-24(21)17(35)8-18(36)25(30)27(38)20-12(29(30)39)4-10(2)6-14(20)32/h3-6,15,17,21,24,31-33,35,37-38H,7-8H2,1-2H3/t15-,17-,21-,24+,30-/m1/s1

InChI Key

FGOBSKJMUFAKJO-ULLJINMFSA-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
Talaromyces islandicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Xanthene
Naphthopyran
1-naphthol
Tetralin
Naphthalene
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Pyran
Vinylogous acid
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Polyol
Ether
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.4	ChemAxon
pKa (Strongest Acidic)	5.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	181.82 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	141.56 m³·mol⁻¹	ChemAxon
Polarizability	53.85 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

101772745

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Saha N, Mondal A, Witte K, Singh SK, Muller M, Husain SM: Monomeric Dihydroanthraquinones: A Chemoenzymatic Approach and its (Bio)synthetic Implications for Bisanthraquinones. Chemistry. 2018 Jan 26;24(6):1283-1286. doi: 10.1002/chem.201705998. Epub 2018 Jan 11. [PubMed:29266494 ]
Nicolaou KC, Papageorgiou CD, Piper JL, Chadha RK: The cytoskyrin cascade: a facile entry into cytoskyrin A, deoxyrubroskyrin, rugulin, skyrin, and flavoskyrin model systems. Angew Chem Int Ed Engl. 2005 Sep 12;44(36):5846-51. doi: 10.1002/anie.200502011. [PubMed:16123947 ]
Snider BB, Gao X: Efficient syntheses of rugulosin analogues. J Org Chem. 2005 Aug 19;70(17):6863-9. doi: 10.1021/jo0508898. [PubMed:16095306 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione (NP0219014)

MOL for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

3D MOL for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

3D SDF for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

3D-SDF for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

PDB for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

3D PDB for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

SMILES for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

INCHI for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

Structure for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)

3D Structure for NP0219014 ((1s,2r,3r,15r,28r)-3,7,9,22,24,28-hexahydroxy-11,20-dimethyl-16-oxaheptacyclo[15.11.1.0²,¹⁵.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³.0²⁵,²⁹]nonacosa-6,8,10,12,17(29),18,20,22,24-nonaene-5,14,26-trione)