NP-MRD: Showing NP-Card for (17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one (NP0241325)

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Record Information

Version

2.0

Created at

2022-09-07 01:22:48 UTC

Updated at

2022-09-07 01:22:48 UTC

NP-MRD ID

NP0241325

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one

Description

(17S,18S,19R)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]Pentacosa-1(25),2(15),4(13),5(10),6,11,21,23-octaen-14-one belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. (17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one is found in Artocarpus obtusus. Based on a literature review very few articles have been published on (17S,18S,19R)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]Pentacosa-1(25),2(15),4(13),5(10),6,11,21,23-octaen-14-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072203222D          

 33 38  0  0  1  0            999 V2000
    1.7471    2.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453    1.2133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7379    0.9845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3324    1.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3232    0.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1158    0.2981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    0.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5029    0.6413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0974    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8992    2.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1066    2.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9084    3.0439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5121    1.6710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7195    1.8998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213    2.7006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8900    0.9845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0882    0.1837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8424    0.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5483   -0.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4937   -0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7011   -0.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7287   -0.0451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9268   -0.8460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7195   -1.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3324   -1.4180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5397   -1.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453   -1.7612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3416   -0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9360    0.1837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5489   -0.1595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3508    0.6413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5581    0.8701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
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  3  4  1  6  0  0  0
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 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  1  0  0  0
M  END

     RDKit          3D

 55 60  0  0  0  0  0  0  0  0999 V2000
   -5.4171   -1.4276    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7336   -0.2244    0.3964 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3940   -0.7049   -0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5169   -1.2475    0.8714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0819   -0.9482    0.7640 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7031    0.1958   -0.2629 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5516   -0.3528    0.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9188   -0.0762    0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8040   -0.6454    1.4410 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3626   -1.5248    2.4296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0280   -1.8077    2.4910 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5097   -2.6721    3.4445 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1304   -1.2249    1.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2096   -1.5341    1.6729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5978   -2.3224    2.5606 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1555   -0.3278    1.3403 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7147    0.5396    0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4614    1.6509    1.1173 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7174   -0.2373   -0.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7245    1.1178   -0.5340 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4093    0.8386   -0.4729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4921    0.5225   -1.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0272    1.4200   -2.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3323    1.6899   -2.1309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045    2.0122   -2.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2512    1.7358   -2.9442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1430    2.3307   -3.8320 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7234    0.8598   -2.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.8109   -0.3987   -0.7989 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4868   -1.1493    1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6833   -1.6109   -0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5878   -2.3916    0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8345   -0.8817    1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0878   -1.9507    3.1104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1595   -3.0883    4.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4930    1.3461    1.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9059    1.9743    2.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5654    2.5150    0.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2969   -1.2667   -0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7902    0.2235   -1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7143   -0.2542    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0271    1.8043   -1.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7443    1.2991   -1.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6728    2.3446   -2.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5437    2.7040   -3.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5025    0.2225   -1.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
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  2 32  1  0
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 22 21  2  0
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 15  5  1  0
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 23 30  1  0
 14  8  1  0
 10  9  1  0
  1 34  1  0
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  2 37  1  1
 32 54  1  1
 33 55  1  0
  3 38  1  6
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  4 40  1  0
 22 50  1  0
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 19 43  1  0
 19 44  1  0
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 20 47  1  0
 20 48  1  0
 11 41  1  0
 13 42  1  0
 25 51  1  0
 26 52  1  0
 28 53  1  0
M  END


  Mrv1652309072203222D          

 33 38  0  0  1  0            999 V2000
    1.7471    2.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453    1.2133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7379    0.9845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3324    1.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3232    0.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1158    0.2981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    0.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5029    0.6413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0974    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8992    2.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1066    2.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9084    3.0439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5121    1.6710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7195    1.8998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213    2.7006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8900    0.9845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4937   -0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7011   -0.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7287   -0.0451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9268   -0.8460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7195   -1.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3324   -1.4180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5397   -1.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453   -1.7612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3416   -0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9360    0.1837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5489   -0.1595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3508    0.6413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5581    0.8701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
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 32 33  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0241325

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H](O)OC2=C3[C@H]1CC1=C(OC4=C5C=CC(C)(C)OC5=CC(O)=C4C1=O)C3=C(O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H22O8/c1-9-11-6-12-20(29)19-14(27)8-16-10(4-5-25(2,3)33-16)21(19)31-22(12)18-13(26)7-15(28)23(17(11)18)32-24(9)30/h4-5,7-9,11,24,26-28,30H,6H2,1-3H3/t9-,11-,24+/m0/s1

> <INCHI_KEY>
HJCJLRPBKUXWKA-SRKHIJOISA-N

> <FORMULA>
C25H22O8

> <MOLECULAR_WEIGHT>
450.443

> <EXACT_MASS>
450.131467668

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
46.95325172960676

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(17S,18S,19R)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0^{2,15}.0^{4,13}.0^{5,10}.0^{21,25}]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one

> <JCHEM_LOGP>
3.5947716110000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.616815277688053

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.527763927536507

> <JCHEM_PKA_STRONGEST_BASIC>
-4.122585824479338

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
119.74029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(17S,18S,19R)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0^{2,15}.0^{4,13}.0^{5,10}.0^{21,25}]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one

> <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       3.261   3.760   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.631   2.265   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.111   1.838   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.220   2.906   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.700   2.478   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.070   0.984   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.549   0.556   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.659   1.624   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.139   1.197   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.248   2.265   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.879   3.760   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.399   4.187   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.029   5.682   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.289   3.119   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.810   3.546   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.440   5.041   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      14.728   1.838   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.098   0.343   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.506   0.967   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.957  -0.935   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.988  -0.725   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.509  -0.298   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.960  -0.084   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.330  -1.579   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.810  -2.006   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.220  -2.647   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.741  -2.220   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.631  -3.288   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.371  -0.725   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.481   0.343   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.891  -0.298   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.521   1.197   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.042   1.624   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4   30                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   22                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    8   15                                                  
CONECT   15   14    5   16                                                  
CONECT   16   15                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21    9                                                       
CONECT   23    6   24   30                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29   23    3                                                  
CONECT   31   29   32                                                       
CONECT   32   31    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₂O₈

Average Mass

450.4430 Da

Monoisotopic Mass

450.13147 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](O)OC2=C3[C@H]1CC1=C(OC4=C5C=CC(C)(C)OC5=CC(O)=C4C1=O)C3=C(O)C=C2O

InChI Identifier

InChI=1S/C25H22O8/c1-9-11-6-12-20(29)19-14(27)8-16-10(4-5-25(2,3)33-16)21(19)31-22(12)18-13(26)7-15(28)23(17(11)18)32-24(9)30/h4-5,7-9,11,24,26-28,30H,6H2,1-3H3/t9-,11-,24+/m0/s1

InChI Key

HJCJLRPBKUXWKA-SRKHIJOISA-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
Artocarpus obtusus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
Naphthopyranone
Naphthopyran
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
1-naphthol
Naphthalene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Vinylogous acid
Heteroaromatic compound
Hemiacetal
Polyol
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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

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

163003826

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one (NP0241325)

MOL for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

3D MOL for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

3D SDF for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

3D-SDF for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

PDB for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

3D PDB for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

SMILES for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

INCHI for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

Structure for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)

3D Structure for NP0241325 ((17s,18s,19r)-12,19,22,24-tetrahydroxy-8,8,18-trimethyl-3,9,20-trioxahexacyclo[15.7.1.0²,¹⁵.0⁴,¹³.0⁵,¹⁰.0²¹,²⁵]pentacosa-1(24),2(15),4,6,10,12,21(25),22-octaen-14-one)