NP-MRD: Showing NP-Card for 1,9-Dideoxyforskolin (NP0065156)

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Record Information

Version

2.0

Created at

2022-04-28 09:25:06 UTC

Updated at

2022-04-28 09:25:07 UTC

NP-MRD ID

NP0065156

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,9-Dideoxyforskolin

Description

1,9-Dideoxyforskolin belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Thus, 1,9-dideoxyforskolin is considered to be an isoprenoid. 1,9-Dideoxyforskolin is found in Coleus forskohlii. Based on a literature review very few articles have been published on 1,9-dideoxyforskolin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282211252D          

 27 29  0  0  1  0            999 V2000
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8678   -0.7993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308   -1.1265    0.0000 C   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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
  9 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  6  0  0  0
 19 20  2  0  0  0  0
 17 21  1  1  0  0  0
 21 22  2  0  0  0  0
 17 23  1  6  0  0  0
  8 24  1  6  0  0  0
  5 25  1  6  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
    3.7945   -0.4806    2.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0106   -1.2135    2.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9973   -0.9293    0.5198 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4721   -0.6509    0.1783 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6158   -2.1591   -0.2003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1375   -2.2608   -0.4701 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -3.2375   -0.9839 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3869   -1.0511   -0.0351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0751   -1.1079   -0.3763 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3654   -1.7215   -1.6863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6658   -2.0782    0.6723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1667   -2.1199    0.5811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6740   -0.7672    1.0178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1641    0.2910    0.0286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4675    1.6263    0.7403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9926    0.2245   -1.1712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6975    0.2073   -0.0716 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0292    1.3863   -0.7117 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1437    1.5349   -2.0319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4060    1.4029   -0.1816 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0920    2.5516   -0.5467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5002    3.4631    0.4135 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2350    4.7075    0.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454    3.2472    1.6389 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1540    0.1230   -0.4917 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6910    0.0761   -1.8890 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3074    0.2002    0.3302 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8036   -0.6833    3.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4216    0.3171    2.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4052   -1.9848    2.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1037   -1.2962    0.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6860   -0.9977   -0.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7399    0.3937    0.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -2.3542   -1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8332   -3.0475    0.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -1.0616    1.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5403   -2.8411   -1.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2583   -1.3487   -2.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5297   -1.6352   -2.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3755   -1.7383    1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2387   -3.0758    0.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5124   -2.8513    1.3302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5418   -2.4371   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7692   -0.7549    0.9465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3641   -0.5615    2.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5009    1.5033    1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5179    2.4540    0.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7772    1.7911    1.5741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4010   -0.8244   -1.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9432    0.8164   -0.9819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5978    0.6350   -2.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3872    0.3499    1.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4973    2.2951   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2685    0.7916   -2.6202 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2845    1.4018    0.9284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9685    5.5159    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8785    5.0621   -0.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3299    4.5908    0.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7473   -0.9133   -2.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7423    0.4932   -1.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1198    0.7317   -2.6049 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 24  2  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17 14  1  0
 14 15  1  1
 14 16  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  6
  9  8  1  0
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  3  1  0
  3  4  1  6
  3 27  1  0
 27 25  1  0
 25 26  1  6
  3  2  1  0
  2  1  2  3
 25 20  1  0
  9 17  1  0
 25  8  1  0
 23 56  1  0
 23 57  1  0
 23 58  1  0
 20 55  1  1
 18 53  1  1
 19 54  1  0
 17 52  1  1
 15 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 16 51  1  0
 13 44  1  0
 13 45  1  0
 12 42  1  0
 12 43  1  0
 11 40  1  0
 11 41  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
  8 36  1  1
  5 34  1  0
  5 35  1  0
  4 31  1  0
  4 32  1  0
  4 33  1  0
 26 59  1  0
 26 60  1  0
 26 61  1  0
  2 30  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652304282211252D          

 27 29  0  0  1  0            999 V2000
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8678   -0.7993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.7998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308   -1.1265    0.0000 C   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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
  9 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  6  0  0  0
 19 20  2  0  0  0  0
 17 21  1  1  0  0  0
 21 22  2  0  0  0  0
 17 23  1  6  0  0  0
  8 24  1  6  0  0  0
  5 25  1  6  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065156

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O5/c1-8-20(5)12-14(24)16-21(6)11-9-10-19(3,4)17(21)15(25)18(26-13(2)23)22(16,7)27-20/h8,15-18,25H,1,9-12H2,2-7H3/t15-,16+,17-,18-,20-,21+,22-/m0/s1

> <INCHI_KEY>
ZKZMDXUDDJYAIB-SUCLLAFCSA-N

> <FORMULA>
C22H34O5

> <MOLECULAR_WEIGHT>
378.509

> <EXACT_MASS>
378.240624195

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
41.91490612755714

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4aS,5S,6S,6aS,10aS,10bR)-3-ethenyl-6-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-5-yl acetate

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
3.1784443343333324

> <ALOGPS_LOGS>
-4.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.806764586713335

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.803037610627136

> <JCHEM_PKA_STRONGEST_BASIC>
-3.322258123548562

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
101.7066

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.48e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,9-dideoxyforskolin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.184  -3.231   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.874  -4.565   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.414  -4.565   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.104  -5.898   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.564  -0.564   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.874   3.437   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.566   0.047   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.620  -1.492   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.566   1.493   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -1.897   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.030  -1.380   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.777  -2.103   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   26   27                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   25                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   19                                                  
CONECT    8    7    9   16   24                                             
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    8   17                                                       
CONECT   17   16   18   21   23                                             
CONECT   18   17   19                                                       
CONECT   19   18    7   20                                                  
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21                                                            
CONECT   23   17                                                            
CONECT   24    8                                                            
CONECT   25    5                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₅

Average Mass

378.5090 Da

Monoisotopic Mass

378.24062 Da

IUPAC Name

(3R,4aS,5S,6S,6aS,10aS,10bR)-3-ethenyl-6-hydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-5-yl acetate

Traditional Name

1,9-dideoxyforskolin

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H34O5/c1-8-20(5)12-14(24)16-21(6)11-9-10-19(3,4)17(21)15(25)18(26-13(2)23)22(16,7)27-20/h8,15-18,25H,1,9-12H2,2-7H3/t15-,16+,17-,18-,20-,21+,22-/m0/s1

InChI Key

ZKZMDXUDDJYAIB-SUCLLAFCSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Plectranthus barbatus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Polycyclic triterpenoid
Naphthopyran
Naphthalene
Oxane
Pyran
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

organic heterotricyclic compound (CHEBI:50295 )
acetate ester (CHEBI:50295 )
labdane diterpenoid (CHEBI:50295 )
Labdane and halimane diterpenoids (LMPR0104030009 )

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	3.18	ALOGPS
logP	3.18	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	13.8	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	101.71 m³·mol⁻¹	ChemAxon
Polarizability	41.91 Å³	ChemAxon
Number of Rings	3	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

C00022264

Chemspider ID

97070

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

107948

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1,9-Dideoxyforskolin (NP0065156)

MOL for NP0065156 (1,9-Dideoxyforskolin)

3D MOL for NP0065156 (1,9-Dideoxyforskolin)

3D SDF for NP0065156 (1,9-Dideoxyforskolin)

3D-SDF for NP0065156 (1,9-Dideoxyforskolin)

PDB for NP0065156 (1,9-Dideoxyforskolin)

3D PDB for NP0065156 (1,9-Dideoxyforskolin)

SMILES for NP0065156 (1,9-Dideoxyforskolin)

INCHI for NP0065156 (1,9-Dideoxyforskolin)

Structure for NP0065156 (1,9-Dideoxyforskolin)

3D Structure for NP0065156 (1,9-Dideoxyforskolin)