NP-MRD: Showing NP-Card for (1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid (NP0172331)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 09:13:06 UTC

Updated at

2022-09-03 09:13:06 UTC

NP-MRD ID

NP0172331

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid

Description

NSC734355 belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid is found in Guilandina bonduc. Based on a literature review very few articles have been published on NSC734355.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032211132D          

 29 32  0  0  1  0            999 V2000
    4.1730   -3.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6412   -2.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8291   -3.0076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215   -2.0864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5776   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5133   -0.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3241    0.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -0.0491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6064    0.5816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185    0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2306    0.8721    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5109    1.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624    0.2414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5745    0.3866    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8548    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230    1.7932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6670    1.3077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -1.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -0.5346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6700   -0.6798    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2018   -1.3105    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 14  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  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
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
   -1.5084    4.7195    0.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8924    3.3095    0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7239    2.9576    1.6321 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4076    2.2835   -0.0676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871    0.9288    0.0809 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6053    0.5904   -1.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2108   -0.7657   -1.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428   -1.7244   -0.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0873   -1.8692    1.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5571   -3.1175   -0.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9984   -1.3426   -0.2780 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6875   -1.1044   -1.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0732   -2.4253    0.1517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401   -2.0576   -0.1037 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0736   -2.8043    0.8803 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162   -0.6489    0.0484 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8877   -0.2232   -0.8175 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8662   -1.2090   -1.1817 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8915   -2.3696   -0.7785 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8791   -0.8273   -2.0686 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596    0.9552   -0.1204 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7243    1.3797    0.1702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5716    2.5832    0.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3075    2.8206    0.9604 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853    1.8720    0.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144    1.7239    0.2453 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6529    0.3922   -0.2116 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6837   -0.0143    0.3888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4480   -0.1293    1.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    4.9615    1.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0981    4.9210   -0.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4110    5.3847    0.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5098    0.9254    0.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0662    0.8471   -2.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4667    1.3269   -1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2663   -0.7372   -0.7049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3474   -1.1704   -2.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0494   -2.9267    1.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980   -1.7058    0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8007   -1.2348    1.8938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9388   -3.2740   -1.7411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4331   -3.9042   -0.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6277   -3.2013   -1.1830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3282   -1.4187   -2.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2677   -2.8125    1.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3181   -3.3143   -0.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6224   -2.4464   -1.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2705   -2.2097    1.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0731   -0.5068    1.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4202    0.1494   -1.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5703   -0.3304   -2.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6816    0.9549   -0.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3607    3.2046    1.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8402    2.4684   -0.5671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6818    2.0749    1.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4948    0.3731   -1.3283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5449    0.3082    2.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4471   -1.1368    2.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1926    0.5467    2.3848 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  8 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 27  1  0
 27 26  1  0
 26 25  1  0
 25 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 21 17  1  0
 17 18  1  0
 18 20  1  0
 18 19  2  0
 27 28  1  0
 28 29  1  1
 28  5  1  0
 28 11  1  0
 17 16  1  0
 24 25  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  1
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  6
 15 48  1  0
 16 49  1  1
 27 56  1  6
 26 54  1  0
 26 55  1  0
 22 52  1  0
 23 53  1  0
 17 50  1  6
 20 51  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
M  END


  Mrv1652309032211132D          

 29 32  0  0  1  0            999 V2000
    4.1730   -3.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6412   -2.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8291   -3.0076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215   -2.0864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5776   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5133   -0.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3241    0.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -0.0491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6064    0.5816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185    0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2306    0.8721    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5109    1.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624    0.2414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5745    0.3866    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8548    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230    1.7932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6670    1.3077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -1.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -0.5346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6700   -0.6798    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2018   -1.3105    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 14  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  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
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0172331

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CCC(C)(C)[C@]2(O)C[C@H](O)[C@@H]3[C@H](CC4=C(C=CO4)[C@H]3C(O)=O)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-11(23)29-16-5-7-20(2,3)22(27)10-14(24)18-13(21(16,22)4)9-15-12(6-8-28-15)17(18)19(25)26/h6,8,13-14,16-18,24,27H,5,7,9-10H2,1-4H3,(H,25,26)/t13-,14-,16-,17+,18-,21-,22+/m0/s1

> <INCHI_KEY>
KBZHBWNGYVPFTP-SSWVEASGSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.67414695478186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S,7R,9S,10R,11S)-3-(acetyloxy)-7,9-dihydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylic acid

> <ALOGPS_LOGP>
1.78

> <JCHEM_LOGP>
1.2639595309999996

> <ALOGPS_LOGS>
-3.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.83908978123026

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.598159287588697

> <JCHEM_PKA_STRONGEST_BASIC>
-2.823840196072052

> <JCHEM_POLAR_SURFACE_AREA>
117.20000000000002

> <JCHEM_REFRACTIVITY>
102.40779999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.77e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,7R,9S,10R,11S)-3-(acetyloxy)-7,9-dihydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       7.790  -6.520   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.797  -5.343   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.281  -5.614   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.320  -3.895   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.327  -2.717   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.811  -2.988   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.819  -1.811   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.342  -0.363   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.825  -0.099   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.338   1.177   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.858  -0.092   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.865   1.086   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.381   1.357   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.897   1.628   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.420   3.076   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.890   0.451   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.406   0.722   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.929   2.170   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.936   3.347   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      12.445   2.441   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.399  -0.456   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.938  -0.506   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.366  -1.985   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.091  -2.849   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.875  -1.904   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.359  -2.175   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.367  -0.998   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.851  -1.269   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.843  -2.446   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   13   28                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   27                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   17   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   16   28                                                  
CONECT   28   27    5   11   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₇

Average Mass

406.4750 Da

Monoisotopic Mass

406.19915 Da

IUPAC Name

(1S,2S,3S,7R,9S,10R,11S)-3-(acetyloxy)-7,9-dihydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylic acid

Traditional Name

(1S,2S,3S,7R,9S,10R,11S)-3-(acetyloxy)-7,9-dihydroxy-2,6,6-trimethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-12(16),13-diene-11-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CCC(C)(C)[C@]2(O)C[C@H](O)[C@@H]3[C@H](CC4=C(C=CO4)[C@H]3C(O)=O)[C@@]12C

InChI Identifier

InChI=1S/C22H30O7/c1-11(23)29-16-5-7-20(2,3)22(27)10-14(24)18-13(21(16,22)4)9-15-12(6-8-28-15)17(18)19(25)26/h6,8,13-14,16-18,24,27H,5,7,9-10H2,1-4H3,(H,25,26)/t13-,14-,16-,17+,18-,21-,22+/m0/s1

InChI Key

KBZHBWNGYVPFTP-SSWVEASGSA-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
Guilandina bonduc	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Naphthofuran
Benzofuran
Dicarboxylic acid or derivatives
Cyclic alcohol
Heteroaromatic compound
Furan
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen 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
logP	1.78	ALOGPS
logP	1.26	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	117.2 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.41 m³·mol⁻¹	ChemAxon
Polarizability	42.67 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

28284114

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24205117

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid (NP0172331)

MOL for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

3D MOL for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

3D SDF for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

3D-SDF for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

PDB for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

3D PDB for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

SMILES for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

INCHI for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

Structure for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)

3D Structure for NP0172331 ((1s,4ar,6s,6ar,7s,11as,11bs)-1-(acetyloxy)-4a,6-dihydroxy-4,4,11b-trimethyl-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-7-carboxylic acid)