NP-MRD: Showing NP-Card for (1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate (NP0223110)

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Record Information

Version

2.0

Created at

2022-09-06 01:06:49 UTC

Updated at

2022-09-06 01:06:49 UTC

NP-MRD ID

NP0223110

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate

Description

(1R,2R,3S,4S,5R,6S,11S,12R,14R,16R,17R,18R,19R,20R,24R)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]Hexacosan-18-yl acetate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. (1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate is found in Chukrasia tabularis. Based on a literature review very few articles have been published on (1R,2R,3S,4S,5R,6S,11S,12R,14R,16R,17R,18R,19R,20R,24R)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]Hexacosan-18-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062203062D          

 44 52  0  0  1  0            999 V2000
    5.4582    2.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3133    1.2879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.0072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9442    0.7563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7993   -0.0559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0373   -0.3931    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4455    0.1817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6648   -1.3058    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4681   -0.3536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2937   -0.8506    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1370   -0.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -1.2721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7796   -2.2047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8569   -2.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1454   -3.1038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5187   -3.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9275   -3.4858    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1330   -4.2848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3982   -2.8164    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8980   -3.4728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2104   -2.5258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8408   -3.0580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569   -1.6977    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3529   -0.9042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2152   -1.4406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8204   -2.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6086   -1.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2138   -2.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7915   -0.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1862   -0.3923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3691    0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8258    1.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2483    1.7416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0528    1.5587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1274    0.7371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3981   -0.6362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5900    0.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222   -2.0577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1124   -1.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0842   -0.8068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465   -0.4374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623   -0.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4911   -0.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6543   -1.6487    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 10 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 35  2  0  0  0  0
 30 36  1  0  0  0  0
  5 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  6  0  0  0
 15 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 44 43  1  6  0  0  0
 38 44  1  0  0  0  0
 13 44  1  0  0  0  0
  8 44  1  0  0  0  0
M  END


  Mrv1652309062203062D          

 44 52  0  0  1  0            999 V2000
    5.4582    2.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3133    1.2879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.0072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9442    0.7563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7993   -0.0559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0373   -0.3931    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4455    0.1817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6648   -1.3058    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4681   -0.3536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2937   -0.8506    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1370   -0.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3811   -1.2721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7796   -2.2047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8569   -2.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1454   -3.1038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5187   -3.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9275   -3.4858    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1330   -4.2848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3982   -2.8164    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8980   -3.4728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2104   -2.5258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8408   -3.0580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569   -1.6977    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3529   -0.9042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2152   -1.4406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8204   -2.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6086   -1.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2138   -2.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7915   -0.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1862   -0.3923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3691    0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8258    1.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2483    1.7416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0528    1.5587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1274    0.7371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3981   -0.6362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5900    0.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222   -2.0577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1124   -1.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0842   -0.8068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465   -0.4374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623   -0.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4911   -0.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6543   -1.6487    0.0000 C   0  0  1  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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 10 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 35  2  0  0  0  0
 30 36  1  0  0  0  0
  5 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  6  0  0  0
 15 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 44 43  1  6  0  0  0
 38 44  1  0  0  0  0
 13 44  1  0  0  0  0
  8 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223110

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1[C@@H](O)[C@@]23O[C@@]4(C)O[C@@]2([C@H](O)[C@@]2(O)[C@@H](O)[C@]5(C)C[C@@]2(O4)[C@]32COC(=O)C[C@@H]52)[C@@H]2CC(=O)O[C@@H](C3=COC=C3)[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H34O14/c1-12(31)40-20-18(34)30-26-11-39-16(32)7-14(26)23(2)10-27(26)28(37,21(23)35)22(36)29(30,43-25(4,42-27)44-30)15-8-17(33)41-19(24(15,20)3)13-5-6-38-9-13/h5-6,9,14-15,18-22,34-37H,7-8,10-11H2,1-4H3/t14-,15+,18+,19-,20-,21-,22+,23+,24+,25+,26+,27+,28-,29+,30-/m0/s1

> <INCHI_KEY>
UDYRKFWKABPBEK-AHLJRIKYSA-N

> <FORMULA>
C30H34O14

> <MOLECULAR_WEIGHT>
618.588

> <EXACT_MASS>
618.194855775

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
58.55371827929493

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3S,4S,5R,6S,11S,12R,14R,16R,17R,18R,19R,20R,24R)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1^{5,12}.0^{1,16}.0^{3,12}.0^{6,11}.0^{11,16}.0^{19,24}]hexacosan-18-yl acetate

> <JCHEM_LOGP>
-1.3432412340000015

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.788255088136527

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.7020567109769

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8625244480568415

> <JCHEM_POLAR_SURFACE_AREA>
200.65

> <JCHEM_REFRACTIVITY>
136.77149999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3S,4S,5R,6S,11S,12R,14R,16R,17R,18R,19R,20R,24R)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1^{5,12}.0^{1,16}.0^{3,12}.0^{6,11}.0^{11,16}.0^{19,24}]hexacosan-18-yl acetate

> <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      10.189   3.920   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.918   2.404   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.470   1.880   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.096   1.412   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.825  -0.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.403  -0.734   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.298   0.339   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.708  -2.437   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.340  -0.660   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.015  -1.588   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.722  -0.076   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.311  -2.375   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.055  -4.115   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.333  -4.857   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.871  -5.794   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.702  -6.795   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.331  -6.507   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.715  -7.998   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.210  -5.257   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.143  -6.483   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.726  -4.715   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.903  -5.708   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.999  -3.169   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.992  -1.688   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.602  -2.689   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.731  -3.736   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.203  -3.281   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      15.332  -4.327   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      14.544  -1.779   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      13.414  -0.732   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.756   0.769   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.741   1.928   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.530   3.251   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      15.032   2.910   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      15.171   1.376   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.943  -1.188   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.301   0.310   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.268  -3.841   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.943  -3.049   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.890  -1.506   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       2.513  -0.816   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       5.156  -0.625   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       6.517  -1.306   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.821  -3.078   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   36                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   23   44                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   12   24                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   19   44                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   17   38                                             
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   13   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    8   24   25                                             
CONECT   24   23   10                                                       
CONECT   25   23   26   36                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   31                                                       
CONECT   36   30    5   25   37                                             
CONECT   37   36                                                            
CONECT   38   15   39   44                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   38   13    8                                             
MASTER        0    0    0    0    0    0    0    0   44    0  104    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3S,4S,5R,6S,11S,12R,14R,16R,17R,18R,19R,20R,24R)-20-(Furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1,.0,.0,.0,.0,.0,]hexacosan-18-yl acetic acid	Generator

Chemical Formula

C₃₀H₃₄O₁₄

Average Mass

618.5880 Da

Monoisotopic Mass

618.19486 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1[C@@H](O)[C@@]23O[C@@]4(C)O[C@@]2([C@H](O)[C@@]2(O)[C@@H](O)[C@]5(C)C[C@@]2(O4)[C@]32COC(=O)C[C@@H]52)[C@@H]2CC(=O)O[C@@H](C3=COC=C3)[C@]12C

InChI Identifier

InChI=1S/C30H34O14/c1-12(31)40-20-18(34)30-26-11-39-16(32)7-14(26)23(2)10-27(26)28(37,21(23)35)22(36)29(30,43-25(4,42-27)44-30)15-8-17(33)41-19(24(15,20)3)13-5-6-38-9-13/h5-6,9,14-15,18-22,34-37H,7-8,10-11H2,1-4H3/t14-,15+,18+,19-,20-,21-,22+,23+,24+,25+,26+,27+,28-,29+,30-/m0/s1

InChI Key

UDYRKFWKABPBEK-AHLJRIKYSA-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
Chukrasia tabularis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Mexicanolide
Limonoid skeleton
Prostaglandin skeleton
Eicosanoid
Naphthopyran
Naphthalene
Tricarboxylic acid or derivatives
Ortho ester
1,3-dioxepane
Carboxylic acid orthoester
Delta valerolactone
Delta_valerolactone
Dioxepane
Pyran
Meta-dioxane
Oxane
Fatty acyl
Meta-dioxolane
Cyclic alcohol
Heteroaromatic compound
Furan
Tertiary alcohol
Carboxylic acid ester
Lactone
Secondary alcohol
Orthocarboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
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

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

163060602

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,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate (NP0223110)

MOL for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

3D MOL for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

3D SDF for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

3D-SDF for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

PDB for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

3D PDB for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

SMILES for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

INCHI for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

Structure for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)

3D Structure for NP0223110 ((1r,2r,3s,4s,5r,6s,11s,12r,14r,16r,17r,18r,19r,20s,24r)-20-(furan-3-yl)-2,3,4,17-tetrahydroxy-5,14,19-trimethyl-8,22-dioxo-9,13,15,21,25-pentaoxaoctacyclo[12.10.1.1⁵,¹².0¹,¹⁶.0³,¹².0⁶,¹¹.0¹¹,¹⁶.0¹⁹,²⁴]hexacosan-18-yl acetate)