NP-MRD: Showing NP-Card for 13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one (NP0328205)

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Record Information

Version

2.0

Created at

2022-09-12 11:27:57 UTC

Updated at

2022-09-12 11:27:57 UTC

NP-MRD ID

NP0328205

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one

Description

13-Chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-2H,3H,3aH,4H,7H,8H,11H,12H,13H,14H,15H,15aH-cyclotetradeca[b]furan-2-one belongs to the class of organic compounds known as cembranolides. These are diterpenoids with a structure based on a cembrane skeleton fused to a lactone ring (5- or 6-membered). 13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one is found in Sarcophyton crassocaule. 13-Chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-2H,3H,3aH,4H,7H,8H,11H,12H,13H,14H,15H,15aH-cyclotetradeca[b]furan-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
   -2.8432   -1.4072   -2.1676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4442   -0.2253   -1.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5661    1.0115   -2.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0897    1.2274   -3.6109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9667    2.0067   -1.7267 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8866    1.6109   -0.3839 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8775    2.2615    0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2329    2.9821   -0.2103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1577    4.0722   -1.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0074    3.5866    0.8118 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1985    2.0638   -0.9315 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2481    3.0383   -2.0175 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.1052    1.3219    0.0250 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4289   -0.0415   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9755   -0.9718    0.4295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682   -0.6870    0.9541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3481   -2.0294    0.9186 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9816   -2.4582    0.5200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0339   -1.9757    1.5633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3549   -2.6002    1.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4089   -4.1026    1.4286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4447   -1.9354    0.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.4868    0.7464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7937    0.0775   -0.4152 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7113   -2.2970   -1.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2908   -1.4924   -3.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9127    1.8090    0.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4139    1.4787    1.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3627    2.9643    1.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7452    4.7333   -1.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4150    3.7379   -2.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9228    4.7196   -0.6821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9046    3.7835    0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6827    1.3188   -1.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0782    1.8457    0.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5861    1.1537    0.9676 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5928   -0.4270   -1.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2724    0.0950   -1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4713   -1.0988    1.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4760    0.4249    1.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1101   -1.1234    0.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8899   -2.6321    1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9792   -3.5700    0.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -2.1127   -0.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3185   -2.3924    2.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0433   -0.8981    1.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033   -4.3120    2.3663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305   -4.5484    1.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8877   -4.5737    0.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3449   -2.5566    0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2286    0.0865    1.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6168   -0.1842    0.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7693   -0.2712   -0.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  2  0
 22 23  1  0
 23 24  1  0
 24  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  1
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
 19 20  1  0
  2 24  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 24 53  1  6
  6 27  1  1
  7 28  1  0
  7 29  1  0
  9 30  1  0
  9 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  6
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1533004161514192D          

 24 25  0  0  0  0            999 V2000
    2.2760   -0.7621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4857    0.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8996    0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1037    0.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5176    0.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7273    1.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5232    1.9949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329    2.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107    2.8608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    3.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5288    3.0101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7385    3.8080    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.1149    2.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9108    2.6468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4969    2.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872    1.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4913    1.0510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2816    0.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2928    2.2835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0333    2.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6054    1.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4033    1.9111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3061    0.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7521    0.2385    0.0000 C   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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  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  2  0  0  0  0
 16 17  1  4  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
 15 19  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0328205

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CCC2C(CC(C)(O)C(Cl)CCC(C)=CCC1)OC(=O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H29ClO3/c1-13-6-5-7-14(2)9-11-18(21)20(4,23)12-17-16(10-8-13)15(3)19(22)24-17/h7-8,16-18,23H,3,5-6,9-12H2,1-2,4H3

> <INCHI_KEY>
AEKUHSZDYHCQSS-UHFFFAOYSA-N

> <FORMULA>
C20H29ClO3

> <MOLECULAR_WEIGHT>
352.9

> <EXACT_MASS>
352.1805225

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
39.26768988359675

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-2H,3H,3aH,4H,7H,8H,11H,12H,13H,14H,15H,15aH-cyclotetradeca[b]furan-2-one

> <ALOGPS_LOGP>
5.09

> <JCHEM_LOGP>
4.539286231

> <ALOGPS_LOGS>
-4.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.940100767616787

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2623999242444173

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
99.18099999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3aH,4H,7H,8H,11H,12H,13H,15H,15aH-cyclotetradeca[b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       4.249  -1.423   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.640   0.067   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.546   1.151   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.060   0.745   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.966   1.829   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.358   3.318   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.843   3.724   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.235   5.213   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.700   5.340   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.093   6.747   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.720   5.619   0.000  0.00  0.00           C+0
HETATM   12 Cl   UNK     0       5.112   7.108   0.000  0.00  0.00          Cl+0
HETATM   13  C   UNK     0       5.815   4.535   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.300   4.941   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.394   3.857   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.003   2.368   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.517   1.962   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.126   0.472   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.880   4.263   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.062   4.151   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.130   3.176   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.619   3.567   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.571   1.741   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.404   0.445   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    2                                                       
CONECT   19   15                                                            
CONECT   20    6   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    5   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₉ClO₃

Average Mass

352.9000 Da

Monoisotopic Mass

352.18052 Da

IUPAC Name

13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-2H,3H,3aH,4H,7H,8H,11H,12H,13H,14H,15H,15aH-cyclotetradeca[b]furan-2-one

Traditional Name

13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3aH,4H,7H,8H,11H,12H,13H,15H,15aH-cyclotetradeca[b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1=CCC2C(CC(C)(O)C(Cl)CCC(C)=CCC1)OC(=O)C2=C

InChI Identifier

InChI=1S/C20H29ClO3/c1-13-6-5-7-14(2)9-11-18(21)20(4,23)12-17-16(10-8-13)15(3)19(22)24-17/h7-8,16-18,23H,3,5-6,9-12H2,1-2,4H3

InChI Key

AEKUHSZDYHCQSS-UHFFFAOYSA-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
Sarcophyton crassocaule	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cembranolides. These are diterpenoids with a structure based on a cembrane skeleton fused to a lactone ring (5- or 6-membered).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Cembranolides

Alternative Parents

Substituents

Cembranolide-skeleton
Cembrane diterpenoid
Diterpenoid
Gamma butyrolactone
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Chlorohydrin
Halohydrin
Lactone
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Alkyl halide
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organohalogen compound
Organochloride
Organooxygen compound
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
logP	5.09	ALOGPS
logP	4.54	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	99.18 m³·mol⁻¹	ChemAxon
Polarizability	39.27 Å³	ChemAxon
Number of Rings	2	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

75066724

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one (NP0328205)

MOL for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

3D MOL for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

3D SDF for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

3D-SDF for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

PDB for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

3D PDB for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

SMILES for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

INCHI for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

Structure for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)

3D Structure for NP0328205 (13-chloro-14-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,13h,15h,15ah-cyclotetradeca[b]furan-2-one)