NP-MRD: Showing NP-Card for (1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol (NP0208535)

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Record Information

Version

2.0

Created at

2022-09-05 05:34:41 UTC

Updated at

2022-09-05 05:34:41 UTC

NP-MRD ID

NP0208535

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol

Description

Agallochaol D belongs to the class of organic compounds known as 17-hydroxysteroids. These are steroids carrying a hydroxyl group at the 17-position of the steroid backbone. (1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol is found in Excoecaria agallocha. Based on a literature review very few articles have been published on Agallochaol D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052207342D          

 24 27  0  0  1  0            999 V2000
    4.7094    0.3328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9960    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119   -0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278    1.3777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3399    1.2325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354    2.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035    1.6682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6232    2.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914    1.8134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5596    1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8399    0.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838    0.8922    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7475    1.3279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0962    0.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867    1.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574    2.0770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8637    2.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    2.1038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1073    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    2.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111    2.5893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3429    3.2200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  2 14  1  0  0  0  0
  8 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  1  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
   -3.8558    1.6150    0.7154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1586    0.2648    0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -0.6609    1.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5327   -0.2566   -0.8049 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9227   -0.5123   -0.7585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8598   -1.5293   -1.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5275   -1.7462   -0.5283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8746   -0.4363   -0.2210 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7849    0.3379   -1.5391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4857   -0.5438    0.3761 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0962    0.8240    0.3404 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2905    1.8380    0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1491    1.7362    0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6982    0.3571    0.7908 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5219    1.0198    0.0650 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1013    2.0139    0.8761 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4841    1.7308    0.8507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4482    0.2316    1.1489 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9804    0.0931    2.4536 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3694   -0.1844    0.1380 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1343   -0.4505   -1.1644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7079   -1.4480    0.5346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3800   -1.5611   -0.2295 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8816   -2.8387    0.1148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9477    1.3633    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5120    2.1549    1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7448    2.1962   -0.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2672   -0.0912    2.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6340   -1.2608    1.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0680   -1.3454    2.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4072    0.5658   -1.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4484    0.2776   -0.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975   -2.4243   -0.9065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7937   -1.5701   -2.2919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8783   -2.2493   -1.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6155   -2.3926    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2923    0.4354   -1.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1495    1.3744   -1.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2879   -0.1853   -2.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3727   -0.7907    1.4636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7188    2.8423    0.5453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3030    2.1159    1.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7651    2.4238    0.2186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4750   -0.1331    1.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5975    1.4365   -0.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8215    1.9279   -0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9901    2.3053    1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4022   -0.2592    0.9618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9192    0.9697    2.9289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5322   -0.2331   -2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4111   -1.5420   -1.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1022    0.0971   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4098   -1.3729    1.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3519   -2.3072    0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5209   -1.4624   -1.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6619   -2.7606    1.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  6
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14  2  1  0
  2  1  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
 11 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 15 20  1  0
 18 20  1  0
  8 10  1  0
  8 14  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 22 54  1  0
 23 55  1  6
 24 56  1  0
 10 40  1  1
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  1
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  6
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
  9 38  1  0
  9 39  1  0
 15 45  1  6
 17 46  1  0
 17 47  1  0
 18 48  1  1
 19 49  1  0
M  END


  Mrv1652309052207342D          

 24 27  0  0  1  0            999 V2000
    4.7094    0.3328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9960    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119   -0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278    1.3777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3399    1.2325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354    2.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035    1.6682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6232    2.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914    1.8134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5596    1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8399    0.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838    0.8922    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7475    1.3279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0962    0.8215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867    1.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574    2.0770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8637    2.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    2.1038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1073    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    2.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111    2.5893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3429    3.2200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  2 14  1  0  0  0  0
  8 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0208535

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12C[C@@H](O)[C@H]3C(=CC[C@H]4C(C)(C)[C@H](O)CC[C@]34C)[C@H]1OC[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O4/c1-18(2)13-6-5-11-16(19(13,3)8-7-14(18)22)12(21)9-20(4)15(23)10-24-17(11)20/h5,12-17,21-23H,6-10H2,1-4H3/t12-,13+,14-,15-,16-,17-,19+,20-/m1/s1

> <INCHI_KEY>
CTPOACOXOBCZPS-SOJUVPGHSA-N

> <FORMULA>
C20H32O4

> <MOLECULAR_WEIGHT>
336.472

> <EXACT_MASS>
336.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
38.26396002977952

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,5R,7R,11R,14S,15R,17R)-2,6,6,15-tetramethyl-12-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-ene-5,14,17-triol

> <JCHEM_LOGP>
1.3710293040000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.88583594376886

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.80317023661916

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8066255415230995

> <JCHEM_POLAR_SURFACE_AREA>
69.92

> <JCHEM_REFRACTIVITY>
92.6691

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5R,7R,11R,14S,15R,17R)-2,6,6,15-tetramethyl-12-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-ene-5,14,17-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.791   0.621   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.459   1.394   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.929  -0.051   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.452   2.572   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.968   2.301   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.929   4.020   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.413   4.291   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.420   3.114   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.897   4.562   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.904   3.385   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.911   2.208   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.434   0.759   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.950   0.488   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.943   1.666   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.395   2.479   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.179   1.534   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.095   2.398   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.667   3.877   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.612   5.093   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.872   3.927   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.200   5.313   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.865   5.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.381   4.833   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.374   6.011   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   14                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   14                                             
CONECT    9    8                                                            
CONECT   10    8   11   23                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    2    8                                                  
CONECT   15   11   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   15   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₄

Average Mass

336.4720 Da

Monoisotopic Mass

336.23006 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@]12C[C@@H](O)[C@H]3C(=CC[C@H]4C(C)(C)[C@H](O)CC[C@]34C)[C@H]1OC[C@H]2O

InChI Identifier

InChI=1S/C20H32O4/c1-18(2)13-6-5-11-16(19(13,3)8-7-14(18)22)12(21)9-20(4)15(23)10-24-17(11)20/h5,12-17,21-23H,6-10H2,1-4H3/t12-,13+,14-,15-,16-,17-,19+,20-/m1/s1

InChI Key

CTPOACOXOBCZPS-SOJUVPGHSA-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
Excoecaria agallocha	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 17-hydroxysteroids. These are steroids carrying a hydroxyl group at the 17-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

17-hydroxysteroids

Alternative Parents

Substituents

Diterpenoid
3-hydroxy-delta-7-steroid
3-hydroxysteroid
11-alpha-hydroxysteroid
17-hydroxysteroid
3-alpha-hydroxysteroid
11-hydroxysteroid
Delta-7-steroid
15-oxasteroid
Naphthofuran
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Polyol
Ether
Oxacycle
Dialkyl ether
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

28282739

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101722985

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol (NP0208535)

MOL for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

3D MOL for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

3D SDF for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

3D-SDF for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

PDB for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

3D PDB for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

SMILES for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

INCHI for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

Structure for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)

3D Structure for NP0208535 ((1s,3ar,5ar,7r,9as,9br,10r,11ar)-6,6,9a,11a-tetramethyl-1h,2h,3ah,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-b]furan-1,7,10-triol)