NP-MRD: Showing NP-Card for 3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate (NP0168774)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 04:38:02 UTC

Updated at

2022-09-03 04:38:02 UTC

NP-MRD ID

NP0168774

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate

Description

10-(Acetyloxy)-2,2,6,9-tetramethyl-1,2,3,3a¹,5,6,7,8,8a,9,10,10a-dodecahydropyren-1-yl acetate belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. 3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate is found in Sinularia nanolobata. 10-(Acetyloxy)-2,2,6,9-tetramethyl-1,2,3,3a¹,5,6,7,8,8a,9,10,10a-dodecahydropyren-1-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231518422D          

 28 31  0  0  0  0            999 V2000
    3.4914   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -0.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
  8 28  1  0  0  0  0
 18 28  1  0  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
   -2.6863    4.4794    0.6435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5768    3.7029    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9659    4.1141   -0.9678 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1245    2.4939    0.5134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0880    1.7356   -0.0239 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5591    0.4214   -0.6056 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0799   -0.7703    0.1190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4334   -2.0039   -0.5180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3851   -3.0082   -0.8029 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8276   -3.0051   -0.5283 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3663   -1.6271   -0.2628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5437   -0.6235   -0.0489 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    0.7439    0.0286 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4324    0.7415    0.7343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3987   -0.2810    0.2759 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8451   -1.5313   -0.2681 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3589   -2.7620    0.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1181    1.5747    0.8503 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7935    2.9105    1.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8666   -2.1741   -0.8638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4099   -0.8930   -1.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7766   -0.6884   -2.8021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9030   -0.9783   -1.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0527    0.2197   -0.4710 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2764   -0.3464    0.8148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1573    0.1884    1.7341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2851   -0.5131    3.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7888    1.2129    1.4309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9918    4.1098    1.6214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5795    4.5411   -0.0056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3028    5.5350    0.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2793    2.3345   -0.9141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2328    0.2878   -1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1756   -0.7403    1.1922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0191   -3.9217   -1.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0830   -3.6930    0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3939   -3.3661   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1400    1.2105   -0.9734 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8955    1.7574    0.5734 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2656    0.6824    1.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1152    0.1718   -0.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600   -0.5434    1.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1703   -1.6909   -1.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6719   -2.9455    1.3525 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3419   -3.6616   -0.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3720   -2.5614    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9556    1.0027    1.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    2.7930    1.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0890    3.7144    1.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3102    3.2119    0.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0306   -2.9682   -1.5990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4914   -2.4310    0.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4471   -1.1416   -3.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6964    0.3828   -3.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8204   -1.2373   -2.8983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1186   -2.0104   -2.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4874   -0.8164   -0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1640   -0.2762   -2.4879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6473    1.1232   -0.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3936   -0.3340    3.6767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3048   -1.6226    2.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1666   -0.2300    3.6089 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 18  1  0
 18 19  1  0
 18  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  6  1  0
  6 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 24 21  1  0
 21 22  1  0
 21 23  1  0
 21 20  1  0
 20  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12  7  1  0
 11 16  1  0
 12 13  1  0
  7  6  1  0
  7  8  1  0
 17 44  1  0
 17 45  1  0
 17 46  1  0
 16 43  1  6
 15 41  1  0
 15 42  1  0
 14 39  1  0
 14 40  1  0
 13 38  1  6
 18 47  1  1
 19 48  1  0
 19 49  1  0
 19 50  1  0
  5 32  1  6
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 33  1  6
 24 59  1  6
 27 60  1  0
 27 61  1  0
 27 62  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
 23 56  1  0
 23 57  1  0
 23 58  1  0
 20 51  1  0
 20 52  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
  7 34  1  1
M  END


  Mrv1533004231518422D          

 28 31  0  0  0  0            999 V2000
    3.4914   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -0.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
  8 28  1  0  0  0  0
 18 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0168774

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2C(C)C(OC(C)=O)C3C(OC(C)=O)C(C)(C)CC4=CCC1=C2C34

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O4/c1-12-7-9-18-13(2)22(27-14(3)25)21-19-16(8-10-17(12)20(18)19)11-24(5,6)23(21)28-15(4)26/h8,12-13,18-19,21-23H,7,9-11H2,1-6H3

> <INCHI_KEY>
NOEYXOCPONNRST-UHFFFAOYSA-N

> <FORMULA>
C24H34O4

> <MOLECULAR_WEIGHT>
386.532

> <EXACT_MASS>
386.245709575

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
43.78919885307614

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(acetyloxy)-2,2,5,8-tetramethyl-1,2,3,3a,3a¹,4,5,5a,6,7,8,9-dodecahydropyren-4-yl acetate

> <ALOGPS_LOGP>
4.87

> <JCHEM_LOGP>
3.5450965553333336

> <ALOGPS_LOGS>
-4.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.7033364488870815

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
108.68449999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a¹,4,5,5a,6,7,8,9-decahydro-1H-pyren-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       6.517  -5.541   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.747  -4.207   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.207  -4.207   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.437  -5.541   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.207  -6.875   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.747  -6.875   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.437  -8.208   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.437  -2.874   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.127  -4.207   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.413  -4.207   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.183  -2.874   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.183  -5.541   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.127  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.052  -2.530   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.052  -0.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.897  -0.206   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.437  -0.206   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.207   1.127   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.747   1.127   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.517  -2.874   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.827  -1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.827   1.127   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.207  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    3    9   28                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   28                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   28                                                  
CONECT   23   22    2   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21   27                                                  
CONECT   27   26                                                            
CONECT   28   22    8   18                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
10-(Acetyloxy)-2,2,6,9-tetramethyl-1,2,3,3a,5,6,7,8,8a,9,10,10a-dodecahydropyren-1-yl acetic acid	Generator
10-(Acetyloxy)-2,2,6,9-tetramethyl-1,2,3,3a¹,5,6,7,8,8a,9,10,10a-dodecahydropyren-1-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₄O₄

Average Mass

386.5320 Da

Monoisotopic Mass

386.24571 Da

IUPAC Name

3-(acetyloxy)-2,2,5,8-tetramethyl-1,2,3,3a,3a¹,4,5,5a,6,7,8,9-dodecahydropyren-4-yl acetate

Traditional Name

3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a¹,4,5,5a,6,7,8,9-decahydro-1H-pyren-4-yl acetate

CAS Registry Number

Not Available

SMILES

CC1CCC2C(C)C(OC(C)=O)C3C(OC(C)=O)C(C)(C)CC4=CCC1=C2C34

InChI Identifier

InChI=1S/C24H34O4/c1-12-7-9-18-13(2)22(27-14(3)25)21-19-16(8-10-17(12)20(18)19)11-24(5,6)23(21)28-15(4)26/h8,12-13,18-19,21-23H,7,9-11H2,1-6H3

InChI Key

NOEYXOCPONNRST-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
Sinularia nanolobata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.87	ALOGPS
logP	3.55	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.68 m³·mol⁻¹	ChemAxon
Polarizability	43.79 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

73798228

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate (NP0168774)

MOL for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

3D MOL for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

3D SDF for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

3D-SDF for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

PDB for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

3D PDB for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

SMILES for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

INCHI for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

Structure for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)

3D Structure for NP0168774 (3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a?,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate)