NP-MRD: Showing NP-Card for (1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one (NP0234584)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 16:41:51 UTC

Updated at

2022-09-06 16:41:51 UTC

NP-MRD ID

NP0234584

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one

Description

(1R,2R,4R,7R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]Pentadecan-6-one belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one is found in Arcangelisia flava. Based on a literature review very few articles have been published on (1R,2R,4R,7R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]Pentadecan-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062218412D          

 28 32  0  0  1  0            999 V2000
    4.8985   -0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1973   -1.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2230   -1.9218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5217   -2.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4703   -0.7071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2124   -1.4908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806   -0.0589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4910    0.5893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    0.7071    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475    0.1768    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6537   -0.5893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9600   -1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3269   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -0.3536    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2041   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3062   -0.8839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021    0.5304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083    1.1786    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1021    1.9446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6977    2.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7522    2.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0139    3.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5419    2.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310    0.2946    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0413    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  9  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 25  2  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
    4.7091    0.7307   -0.7681 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7594    0.5557    0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0823   -0.0136    1.3095 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.7860    1.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3996    0.9866   -0.2771 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4541    1.5176   -1.5625 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0075    2.0526    0.7229 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8791    3.3985    0.1127 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    2.5712    0.5144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0189    1.9170   -0.5850 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0461    0.4178   -0.5872 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4059   -0.1425   -0.3400 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8892   -1.0188   -1.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4996   -1.0271    0.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213   -2.0393    0.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8249   -1.7089    0.2016 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9588   -2.3987    0.9153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8060   -3.4893    1.5130 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1852   -1.7268    0.8559 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3980   -0.9263   -0.2914 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7505   -0.3372   -0.1801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1146    0.9599   -0.4212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4789    1.0266   -0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8808   -0.1673    0.1754 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8942   -1.0194    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3565    0.1240   -0.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0441   -0.2146    0.2394 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1203    0.2277    1.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.4333   -0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5743    1.1688   -1.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2969   -1.1466    2.5034 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3085   -1.6383    0.7553 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1892   -0.1740    1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7254    2.4730   -1.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5097    2.0789    1.7133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566    3.1588    1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2656    2.3360   -1.5944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1033    2.1888   -0.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2324    0.1339   -1.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9828   -0.9646   -1.6081 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4001   -0.6292   -2.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6064   -2.0712   -1.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6494   -0.4131    1.7864 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4644   -1.6076    0.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1733   -2.1933    2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7483   -3.0628    0.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7649   -2.0401   -0.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3695   -1.5946   -1.2013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4763    1.7854   -0.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0662    1.9396   -0.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0067   -2.0604    0.4636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1789    0.3618   -1.5453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7307    1.0568    0.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3404    0.9129    1.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0969    0.7346    1.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1076   -0.6375    2.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 27  1  0
 27 28  1  1
 27 26  1  0
 26 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  6
 20 21  1  0
 21 25  2  0
 25 24  1  0
 24 23  1  0
 23 22  2  0
 12  5  1  0
 22 21  1  0
  9  7  1  0
 12 11  1  0
 16 27  1  0
  4 31  1  0
  4 32  1  0
  4 33  1  0
  1 29  1  0
  1 30  1  0
  6 34  1  0
  7 35  1  1
  9 36  1  1
 10 37  1  0
 10 38  1  0
 11 39  1  6
 28 54  1  0
 28 55  1  0
 28 56  1  0
 26 52  1  0
 26 53  1  0
 20 48  1  6
 16 47  1  6
 15 45  1  0
 15 46  1  0
 14 43  1  0
 14 44  1  0
 13 40  1  0
 13 41  1  0
 13 42  1  0
 25 51  1  0
 23 50  1  0
 22 49  1  0
M  END


  Mrv1652309062218412D          

 28 32  0  0  1  0            999 V2000
    4.8985   -0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1973   -1.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2230   -1.9218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5217   -2.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4703   -0.7071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2124   -1.4908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806   -0.0589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4910    0.5893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    0.7071    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475    0.1768    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6537   -0.5893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9600   -1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3269   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -0.3536    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2041   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3062   -0.8839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021    0.5304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083    1.1786    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1021    1.9446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6977    2.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7522    2.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0139    3.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5419    2.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310    0.2946    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0413    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  9  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 25  2  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0234584

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=C)[C@]1(O)[C@H]2O[C@H]2C[C@@H]2[C@@]3(C)C[C@@H](OC(=O)[C@@H]3CC[C@]12C)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O6/c1-12(25-4)22(24)18-15(27-18)9-17-20(2)10-16(13-6-8-26-11-13)28-19(23)14(20)5-7-21(17,22)3/h6,8,11,14-18,24H,1,5,7,9-10H2,2-4H3/t14-,15-,16+,17+,18-,20-,21-,22-/m0/s1

> <INCHI_KEY>
PXDWHOGTDYNMHZ-OTUOGLGPSA-N

> <FORMULA>
C22H28O6

> <MOLECULAR_WEIGHT>
388.46

> <EXACT_MASS>
388.188588622

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
40.58579106059376

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,4R,7R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecan-6-one

> <JCHEM_LOGP>
2.2516506589999983

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.263656113651011

> <JCHEM_PKA_STRONGEST_BASIC>
-2.864004079075981

> <JCHEM_POLAR_SURFACE_AREA>
81.43

> <JCHEM_REFRACTIVITY>
100.0996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4R,7R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecan-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.144  -1.237   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.835  -2.048   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.883  -3.587   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.574  -4.399   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.478  -1.320   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.997  -2.783   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.430  -0.110   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.383   1.100   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.859   1.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.382   0.330   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.954  -1.100   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.525  -2.530   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.477  -2.090   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.905  -0.660   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.381  -0.440   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.572  -1.650   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -0.191   0.990   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.762   2.200   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.191   3.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.302   4.008   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.404   5.545   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.026   6.116   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.011   4.933   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.286   1.980   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.858   0.550   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.811   1.760   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6    7   12                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7    9                                                       
CONECT    9    8    7   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11    5   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21                                                       
CONECT   26   20   27                                                       
CONECT   27   26   16   11   28                                             
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₆

Average Mass

388.4600 Da

Monoisotopic Mass

388.18859 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=C)[C@]1(O)[C@H]2O[C@H]2C[C@@H]2[C@@]3(C)C[C@@H](OC(=O)[C@@H]3CC[C@]12C)C1=COC=C1

InChI Identifier

InChI=1S/C22H28O6/c1-12(25-4)22(24)18-15(27-18)9-17-20(2)10-16(13-6-8-26-11-13)28-19(23)14(20)5-7-21(17,22)3/h6,8,11,14-18,24H,1,5,7,9-10H2,2-4H3/t14-,15-,16+,17+,18-,20-,21-,22-/m0/s1

InChI Key

PXDWHOGTDYNMHZ-OTUOGLGPSA-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
Arcangelisia flava	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthopyran
Naphthalene
Delta valerolactone
Oxepane
Delta_valerolactone
Pyran
Oxane
Cyclic alcohol
Heteroaromatic compound
Tertiary alcohol
Furan
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Oxirane
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Alcohol
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
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

162938141

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one (NP0234584)

MOL for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

3D MOL for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

3D SDF for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

3D-SDF for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

PDB for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

3D PDB for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

SMILES for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

INCHI for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

Structure for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)

3D Structure for NP0234584 ((1r,2r,4r,7r,10s,11r,12s,14s)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]pentadecan-6-one)