NP-MRD: Showing NP-Card for 2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate (NP0198448)

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Record Information

Version

2.0

Created at

2022-09-04 16:54:15 UTC

Updated at

2022-09-04 16:54:15 UTC

NP-MRD ID

NP0198448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate

Description

2,4-Dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]Pentadecane-2,4-dicarboxylate belongs to the class of organic compounds known as c20-gibberellins. These are gibberellins with carboxy groups in positions 7 and 18 and some also in 20, while others have an aldehyde group in the latter position. Based on a literature review very few articles have been published on 2,4-dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]Pentadecane-2,4-dicarboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042218542D          

 28 31  0  0  1  0            999 V2000
   -1.5766   -0.6321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8037   -0.3437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0752   -0.8268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0599   -1.6517    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.6481   -0.3078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0561    0.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5707    0.4953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0966    1.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7653    1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1400    0.4214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9535    0.1957    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8234    1.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6402    0.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3795    0.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4322   -0.5365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1715   -0.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7454   -0.9938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3150   -1.5906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2565   -1.6583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4366   -1.5671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -2.4139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0986   -3.0785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -0.6277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2295   -0.9276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0458   -1.7319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2575   -1.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6506   -2.2930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4670   -3.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  6  1  1  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 11  1  1  0  0  0
 23 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    5.0724    0.3046    0.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7960    0.1177    0.3133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917    0.2967   -0.5610 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6830    1.6110   -0.9809 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.3978    0.0348    0.2928 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9315    0.4232    1.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2689   -0.3328    1.6298 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1069   -1.8116    1.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6687   -2.2374    1.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9772   -1.3985    0.3999 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5157   -1.3082    0.5728 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0058   -0.9444    1.9135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2250   -2.5372    0.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6886   -2.3409   -0.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1830   -1.0430   -0.5605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7450   -1.2061   -1.8508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2535    0.1355   -0.4952 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4371    0.8678   -1.8482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7053    1.1375    0.4931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6034    0.8398    1.3089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663    2.4031    0.5481 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6416    3.3330    1.5239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.2267   -0.4424 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1703    0.8122   -0.1202 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4106    1.7496   -1.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3522    2.9988   -1.1306 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7210    1.2775   -2.5479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9447    2.2072   -3.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8595    0.1477    0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3269    0.6361   -0.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6451   -0.4281   -1.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3463    0.0864    2.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1787    1.4925    1.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9094   -0.0056    2.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6541   -2.2585    0.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5381   -2.3327    2.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2550   -2.2672    2.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6364   -3.2976    1.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1315   -1.8612   -0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0749   -1.3117    1.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0778    0.1431    2.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5075   -1.3912    2.7670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7869   -2.7316   -0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0496   -3.4254    0.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1581   -2.6413    0.8932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0463   -3.1760   -0.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0825   -0.7633    0.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912   -1.7594   -2.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5492    0.9307   -1.9788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0815    1.9025   -1.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0500    0.2738   -2.6719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7522    3.3273    1.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4124    3.0149    2.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2525    4.3466    1.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5415   -0.6548   -1.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0674    1.4509    0.7605 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1624    3.2154   -3.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8757    1.9042   -4.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0668    2.2701   -4.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 25  1  0
 25 26  2  0
 25 24  1  0
 24 23  1  0
 23 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  1
 19 20  2  0
 19 21  1  0
 21 22  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  5  6  1  1
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  5 24  1  0
 17 23  1  0
  5 10  1  0
  2  7  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 24 56  1  1
 23 55  1  6
 12 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  1
 16 48  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 22 52  1  0
 22 53  1  0
 22 54  1  0
 10 39  1  6
  9 37  1  0
  9 38  1  0
  8 35  1  0
  8 36  1  0
  7 34  1  1
  6 32  1  0
  6 33  1  0
  3 31  1  6
  1 29  1  0
  1 30  1  0
M  END


  Mrv1652309042218542D          

 28 31  0  0  1  0            999 V2000
   -1.5766   -0.6321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8037   -0.3437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0752   -0.8268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0599   -1.6517    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.6481   -0.3078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0561    0.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5707    0.4953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0966    1.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7653    1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1400    0.4214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9535    0.1957    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8234    1.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6402    0.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3795    0.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4322   -0.5365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1715   -0.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7454   -0.9938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3150   -1.5906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2565   -1.6583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4366   -1.5671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -2.4139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0986   -3.0785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -0.6277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2295   -0.9276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0458   -1.7319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2575   -1.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6506   -2.2930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4670   -3.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  6  1  1  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 11  1  1  0  0  0
 23 24  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@H]1[C@H]2[C@@](C)(CC[C@H](O)[C@@]2(C)C(=O)OC)[C@@H]2CC[C@@H]3C[C@]12[C@@H](F)C3=C

> <INCHI_IDENTIFIER>
InChI=1S/C22H31FO5/c1-11-12-6-7-13-20(2)9-8-14(24)21(3,19(26)28-5)16(20)15(18(25)27-4)22(13,10-12)17(11)23/h12-17,24H,1,6-10H2,2-5H3/t12-,13+,14+,15-,16+,17+,20+,21-,22-/m1/s1

> <INCHI_KEY>
DAYMQQMZXAMXSG-HFCIBHKPSA-N

> <FORMULA>
C22H31FO5

> <MOLECULAR_WEIGHT>
394.483

> <EXACT_MASS>
394.215552261

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.252480806811796

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,4-dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4-dicarboxylate

> <JCHEM_LOGP>
2.463171824666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.452471084916532

> <JCHEM_PKA_STRONGEST_BASIC>
-3.038289147457509

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
99.72559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2,4-dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.943  -1.180   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.500  -0.642   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.140  -1.543   0.000  0.00  0.00           C+0
HETATM    4  F   UNK     0      -0.112  -3.083   0.000  0.00  0.00           F+0
HETATM    5  C   UNK     0       1.210  -0.575   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.105   0.244   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.065   0.925   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.180   2.287   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.428   2.253   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.128   0.787   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.647   0.365   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.404   1.886   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.928   1.219   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.308   0.535   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.407  -1.002   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.787  -1.685   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.125  -1.855   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.188  -2.969   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.212  -3.095   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.682  -2.925   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.830  -4.506   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.917  -5.746   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.745  -1.172   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.295  -1.731   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.952  -3.233   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.481  -3.687   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       3.081  -4.280   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.738  -5.782   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10   24                                             
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12   13   23                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   23                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23   17   11   24                                                  
CONECT   24   23    5   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
2,4-Dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0,.0,]pentadecane-2,4-dicarboxylic acid	Generator

Chemical Formula

C₂₂H₃₁FO₅

Average Mass

394.4830 Da

Monoisotopic Mass

394.21555 Da

IUPAC Name

2,4-dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4-dicarboxylate

Traditional Name

2,4-dimethyl (1R,2S,3S,4S,5S,8S,9S,12R,14S)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4-dicarboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@H]1[C@H]2[C@@](C)(CC[C@H](O)[C@@]2(C)C(=O)OC)[C@@H]2CC[C@@H]3C[C@]12[C@@H](F)C3=C

InChI Identifier

InChI=1S/C22H31FO5/c1-11-12-6-7-13-20(2)9-8-14(24)21(3,19(26)28-5)16(20)15(18(25)27-4)22(13,10-12)17(11)23/h12-17,24H,1,6-10H2,2-5H3/t12-,13+,14+,15-,16+,17+,20+,21-,22-/m1/s1

InChI Key

DAYMQQMZXAMXSG-HFCIBHKPSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c20-gibberellins. These are gibberellins with carboxy groups in positions 7 and 18 and some also in 20, while others have an aldehyde group in the latter position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

C20-gibberellins

Alternative Parents

Substituents

Gibberellane diterpenoid
Beta-hydroxy acid
Dicarboxylic acid or derivatives
Hydroxy acid
Cyclic alcohol
Methyl ester
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organooxygen compound
Organofluoride
Organohalogen compound
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Alkyl halide
Alkyl fluoride
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.46	ChemAxon
pKa (Strongest Acidic)	14.45	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.73 m³·mol⁻¹	ChemAxon
Polarizability	41.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

162892923

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate (NP0198448)

MOL for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

3D MOL for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

3D SDF for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

3D-SDF for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

PDB for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

3D PDB for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

SMILES for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

INCHI for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

Structure for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)

3D Structure for NP0198448 (2,4-dimethyl (1r,2s,3s,4s,5s,8s,9s,12r,14s)-14-fluoro-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0¹,⁹.0³,⁸]pentadecane-2,4-dicarboxylate)