NP-MRD: Showing NP-Card for (1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate (NP0215801)

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Record Information

Version

2.0

Created at

2022-09-05 15:32:04 UTC

Updated at

2022-09-05 15:32:05 UTC

NP-MRD ID

NP0215801

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate

Description

(1S,3S,4R,6S,8R,9R,10R,11S,14S,15R,17S)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]Heptadecan-3-yl acetate belongs to the class of organic compounds known as grayanoids. These are diterpenoids containing a skeleton based on or derived from the ent-kaurane moiety. Grayanoids usually possess either one of the grayanane, the 2,4-seco-grayanane, the 9,10-seco-grayanane, the 1,5-seco-grayanane, the kalmane, or the leucothane skeleton. Some derivatives also include the 1,5-seco-kalmane skeleton. (1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate is found in Rhododendron molle. Based on a literature review very few articles have been published on (1S,3S,4R,6S,8R,9R,10R,11S,14S,15R,17S)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]Heptadecan-3-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052217322D          

 29 33  0  0  1  0            999 V2000
    2.2056    2.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    2.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0769    3.1518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6221    1.8310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5134    1.0132    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7287    0.7503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3868   -0.0275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6253    0.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9151   -0.0557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1638   -0.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5033    0.6592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1946   -0.8739    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6649   -1.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5193   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765   -0.7646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7079   -0.8534    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4379   -1.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4067   -1.2919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2954   -0.2682    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1030   -0.4367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9280   -0.4335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5128    0.2794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9584    0.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6240    1.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5432    1.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2060    0.5519    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2739    1.3741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8250   -0.4783    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3032   -1.1506    0.0000 O   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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 16 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  6  0  0  0
 22 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
  5 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  1  0  0  0
 12 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          2D

 63 67  0  0  0  0  0  0  0  0999 V2000
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   -5.6055   -2.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4351   -3.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5607   -0.7781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2398   -0.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2267    1.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9588    2.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4347    2.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3849    2.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1154    4.7355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8691    5.5369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5931    4.7483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2587    2.6595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602    2.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9908    4.1354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4330    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8660    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4330   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495   -2.5838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1586   -1.9635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3921   -1.3515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2349    3.3267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7036    3.6313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2473   -3.6990    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2156   -4.3091    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1127    4.9905    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0381    6.1419    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4817    4.2046    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7189    2.9762    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6443    4.2223    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5568    1.9570    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3396   -2.0357    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6394   -3.9542    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4315   -3.5074    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1850   -2.1453    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3566   -2.8663    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7453   -3.4054    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5182   -1.3298    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -2.5908    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.6535    4.7922    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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  9 11  1  1
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 26  5  1  0
 15  7  1  0
 26 19  1  0
 28  7  1  0
 22 20  1  0
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  1 31  1  0
  1 32  1  0
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  6 34  1  0
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 10 38  1  0
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 25 58  1  0
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 25 60  1  0
 27 61  1  0
 28 62  1  6
 29 63  1  0
M  END


  Mrv1652309052217322D          

 29 33  0  0  1  0            999 V2000
    2.2056    2.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    2.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0769    3.1518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6221    1.8310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5134    1.0132    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7287    0.7503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3868   -0.0275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6253    0.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9151   -0.0557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1638   -0.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5033    0.6592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1946   -0.8739    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6649   -1.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5193   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765   -0.7646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7079   -0.8534    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4379   -1.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4067   -1.2919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2954   -0.2682    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1030   -0.4367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9280   -0.4335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5128    0.2794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9584    0.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6240    1.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5432    1.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2060    0.5519    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2739    1.3741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8250   -0.4783    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3032   -1.1506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
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  9 12  1  0  0  0  0
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 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
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M  END
> <DATABASE_ID>
NP0215801

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@]23C[C@@](C)(O)[C@@H](CC[C@@H]2[C@@](C)(O)[C@H]2[C@H]4O[C@H]4C(C)(C)[C@@]12O)[C@@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O7/c1-10(23)28-13-8-21-9-19(4,25)11(16(21)24)6-7-12(21)20(5,26)15-14-17(29-14)18(2,3)22(13,15)27/h11-17,24-27H,6-9H2,1-5H3/t11-,12+,13-,14+,15+,16-,17+,19+,20+,21-,22+/m0/s1

> <INCHI_KEY>
FJISLLRXVSQIES-QZCYQNCWSA-N

> <FORMULA>
C22H34O7

> <MOLECULAR_WEIGHT>
410.507

> <EXACT_MASS>
410.230453435

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
0.0

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,4R,6S,8R,9R,10R,11S,14S,15R,17S)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

> <JCHEM_LOGP>
-0.4254122926666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.041147918132772

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.998963283455438

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9365822713340908

> <JCHEM_POLAR_SURFACE_AREA>
119.75000000000001

> <JCHEM_REFRACTIVITY>
101.59469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4R,6S,8R,9R,10R,11S,14S,15R,17S)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

> <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       4.117   3.769   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.541   4.357   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.743   5.883   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.761   3.418   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.558   1.891   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.094   1.401   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.455  -0.051   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.034   0.841   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.708  -0.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.306  -0.740   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.940   1.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.230  -1.631   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.108  -2.991   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.703  -2.923   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.369  -1.427   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.921  -1.593   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.417  -3.048   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.226  -2.412   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.018  -0.501   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.526  -0.815   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.066  -0.809   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.291   0.521   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.256   1.662   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.498   2.572   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.481   2.993   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.851   1.030   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.978   2.565   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.407  -0.893   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.299  -2.148   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   15   28                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    7   16                                                  
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   26                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   22                                                       
CONECT   22   21   20   23                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23    5   19   27                                             
CONECT   27   26                                                            
CONECT   28   12    7   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
(1S,3S,4R,6S,8R,9R,10R,11S,14S,15R,17S)-4,10,15,17-Tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0,.0,.0,]heptadecan-3-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₄O₇

Average Mass

410.5070 Da

Monoisotopic Mass

410.23045 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@]23C[C@@](C)(O)[C@@H](CC[C@@H]2[C@@](C)(O)[C@H]2[C@H]4O[C@H]4C(C)(C)[C@@]12O)[C@@H]3O

InChI Identifier

InChI=1S/C22H34O7/c1-10(23)28-13-8-21-9-19(4,25)11(16(21)24)6-7-12(21)20(5,26)15-14-17(29-14)18(2,3)22(13,15)27/h11-17,24-27H,6-9H2,1-5H3/t11-,12+,13-,14+,15+,16-,17+,19+,20+,21-,22+/m0/s1

InChI Key

FJISLLRXVSQIES-QZCYQNCWSA-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
Rhododendron molle	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as grayanoids. These are diterpenoids containing a skeleton based on or derived from the ent-kaurane moiety. Grayanoids usually possess either one of the grayanane, the 2,4-seco-grayanane, the 9,10-seco-grayanane, the 1,5-seco-grayanane, the kalmane, or the leucothane skeleton. Some derivatives also include the 1,5-seco-kalmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Grayanoids

Alternative Parents

Substituents

Grayanoid
Oxane
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

138108177

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate (NP0215801)

MOL for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

3D MOL for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

3D SDF for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

3D-SDF for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

PDB for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

3D PDB for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

SMILES for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

INCHI for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

Structure for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)

3D Structure for NP0215801 ((1s,3s,4r,6s,8r,9r,10r,11s,14s,15r,17s)-4,10,15,17-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0¹,¹¹.0⁴,⁹.0⁶,⁸]heptadecan-3-yl acetate)