NP-MRD: Showing NP-Card for 3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate (NP0213289)

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Record Information

Version

2.0

Created at

2022-09-05 12:14:10 UTC

Updated at

2022-09-05 12:14:10 UTC

NP-MRD ID

NP0213289

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate

Description

8-(Acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]Pentadec-2-en-14-yl acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate is found in Jania rubens and Laurencia dendroidea. 8-(Acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]Pentadec-2-en-14-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251512362D          

 30 33  0  0  0  0            999 V2000
    0.3062    3.3589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124    2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021    1.9446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7351    1.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5517    1.5911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    0.7071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7923    1.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4910    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4703   -0.7071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6537   -0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475    0.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8372   -0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310    0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2041   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021    0.5304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033    0.0958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6518    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3940    1.9292    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4594    0.9770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0092    1.5921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7765   -1.4732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4496   -2.0036    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
  2  4  1  0  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
 10 11  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 16 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
    2.8494    4.1753    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0642    3.5416    1.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9221    4.1981   -0.0271 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4869    2.3042    1.1018 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7467    1.7291    0.0506 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6958    1.5061    0.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3536    1.0564   -0.9095 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0152   -0.3785   -1.1146 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.8175   -1.2555   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2799   -1.0648   -0.3758 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9483   -1.6163    0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8146   -2.6668    0.6340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5013   -3.2264    1.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0208   -3.1569   -0.5070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7400    0.3303   -0.5527 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.8155    1.3573   -0.9390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2986    2.4667   -1.8599 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4347   -0.5647   -0.9319 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0290   -1.7603   -1.1536 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4592   -2.0222   -0.9946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950   -1.0715   -0.0900 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1346   -0.2579   -0.9898 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0239   -1.8920    0.8551 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1116   -3.0911   -0.2167 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.8844   -1.1115    1.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1099   -0.2771    2.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2977   -0.0934    0.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3769    0.4949   -0.5003 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4650    5.2266    2.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9111    4.2298    1.8482 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6551    3.6765    3.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8406   -0.3242   -3.2994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5276   -0.5046   -2.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5187   -1.1883    0.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6109   -1.6494   -1.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0267   -2.9063    2.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5708   -2.8926    1.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5088   -4.3519    1.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7821    0.4017   -0.9860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8548    1.1216    1.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2150    2.1876    0.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    3.1084   -2.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6508    2.0671   -2.8186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0187    3.1395   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3751   -2.5655   -1.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5628   -3.0861   -0.6443 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9003   -2.0518   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7769   -0.2794   -2.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1534    0.8082   -0.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1597   -0.6307   -0.9623 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3289   -2.5381    1.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
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 23 25  1  0
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 25 27  1  0
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  7 18  1  0
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 17 16  1  0
 16 11  1  0
 20  8  1  0
 16 18  1  0
 20 30  1  0
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  9 40  1  0
  7 37  1  6
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  6 36  1  0
  5 34  1  6
  1 31  1  0
  1 32  1  0
  1 33  1  0
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 29 63  1  0
 29 64  1  0
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 22 54  1  0
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 19 50  1  0
 19 51  1  0
 19 52  1  0
 17 48  1  0
 17 49  1  0
 16 47  1  6
M  END


  Mrv1533004251512362D          

 30 33  0  0  0  0            999 V2000
    0.3062    3.3589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124    2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021    1.9446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7351    1.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5517    1.5911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    0.7071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7923    1.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4910    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4703   -0.7071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6537   -0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475    0.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8372   -0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310    0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0207   -0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2041   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021    0.5304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8033    0.0958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6518    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3940    1.9292    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4594    0.9770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0092    1.5921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7765   -1.4732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4496   -2.0036    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213289

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2(C)C(CC(OC(C)=O)C3CC(C)(CC=C23)C(Br)CO)C2(C)CC12

> <INCHI_IDENTIFIER>
InChI=1S/C24H35BrO5/c1-13(27)29-18-8-20-23(4)10-17(23)19(30-14(2)28)11-24(20,5)16-6-7-22(3,9-15(16)18)21(25)12-26/h6,15,17-21,26H,7-12H2,1-5H3

> <INCHI_KEY>
SNYAFQIWJMZVCJ-UHFFFAOYSA-N

> <FORMULA>
C24H35BrO5

> <MOLECULAR_WEIGHT>
483.443

> <EXACT_MASS>
482.166787

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
48.83547210660531

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]pentadec-2-en-14-yl acetate

> <ALOGPS_LOGP>
4.25

> <JCHEM_LOGP>
3.007338076666666

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.50579317517607

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0149660651779877

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
117.3776

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]pentadec-2-en-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       0.572   6.270   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.143   4.840   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.191   3.630   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.239   3.190   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.763   2.970   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.859   1.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.079   2.844   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.383   1.100   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.430  -0.110   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.478  -1.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.954  -1.100   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.382   0.330   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.429  -0.880   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.858   0.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.905  -0.660   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.381  -0.440   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.191   0.990   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.500   0.179   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.762   2.200   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.286   1.980   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.217   2.138   0.000  0.00  0.00           C+0
HETATM   24 Br   UNK     0      -0.735   3.601   0.000  0.00  0.00          Br+0
HETATM   25  C   UNK     0      -2.724   1.824   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.750   2.972   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.049  -2.750   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.097  -3.960   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.573  -3.740   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   14                                                  
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    8   12                                                  
CONECT   12   11   13   27                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   23                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    5   16                                                  
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   12   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
8-(Acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0,.0,]pentadec-2-en-14-yl acetic acid	Generator
8-(Acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]pentadec-2-en-14-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₅BrO₅

Average Mass

483.4430 Da

Monoisotopic Mass

482.16679 Da

IUPAC Name

8-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]pentadec-2-en-14-yl acetate

Traditional Name

8-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]pentadec-2-en-14-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2(C)C(CC(OC(C)=O)C3CC(C)(CC=C23)C(Br)CO)C2(C)CC12

InChI Identifier

InChI=1S/C24H35BrO5/c1-13(27)29-18-8-20-23(4)10-17(23)19(30-14(2)28)11-24(20,5)16-6-7-22(3,9-15(16)18)21(25)12-26/h6,15,17-21,26H,7-12H2,1-5H3

InChI Key

SNYAFQIWJMZVCJ-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
Jania rubens	LOTUS Database	35616633
Laurencia dendroidea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Dicarboxylic acid or derivatives
Bromohydrin
Carboxylic acid ester
Halohydrin
Carboxylic acid derivative
Organobromide
Organohalogen compound
Alkyl bromide
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Alkyl halide
Organooxygen compound
Primary alcohol
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	4.25	ALOGPS
logP	3.01	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	14.51	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	6	ChemAxon
Refractivity	117.38 m³·mol⁻¹	ChemAxon
Polarizability	48.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

73838011

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)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate (NP0213289)

MOL for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D MOL for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D SDF for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D-SDF for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

PDB for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D PDB for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

SMILES for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

INCHI for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

Structure for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D Structure for NP0213289 (3-(acetyloxy)-5-(1-bromo-2-hydroxyethyl)-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)