NP-MRD: Showing NP-Card for (1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate (NP0302715)

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Record Information

Version

2.0

Created at

2022-09-10 16:28:47 UTC

Updated at

2022-09-10 16:28:47 UTC

NP-MRD ID

NP0302715

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-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. (1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate is found in Laurencia saitoi. Based on a literature review very few articles have been published on (1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0²,⁷.0¹¹,¹³]Pentadec-2-en-14-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102218282D          

 27 30  0  0  1  0            999 V2000
    0.3402   -0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6464   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1361   -1.5321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4630   -1.0018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7692   -1.7679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5857   -1.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919   -2.6518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4022   -2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2188   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0353   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3415   -3.0054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0428   -2.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8913   -3.6205    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6989   -3.4520    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.6334   -4.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1832   -5.0193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8312   -3.6536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146   -3.5357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5043   -4.1839    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8105   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6878   -4.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5650   -3.1821    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4472   -3.9987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485   -3.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2588   -2.4161    0.0000 C   0  0  1  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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 19 18  1  1  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 23 22  1  6  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 27 26  1  1  0  0  0
  5 27  1  0  0  0  0
 24 27  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    5.6843    0.1720    3.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8502    0.7022    2.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9894    1.9167    2.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9357   -0.0317    1.6816 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1335    0.5094    0.6184 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7094    0.3633    1.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7953   -0.0852   -0.0967 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8685   -1.5951   -0.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6326    0.2682    0.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0331    0.5473    1.4014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4304    0.8940    1.6810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4306    0.4162    0.6895 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6407    1.3642    0.7956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9068   -0.9488    1.1261 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4813   -2.2572    0.9659 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -5.0853   -1.4588    0.3341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1842   -0.5944    0.4503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9722    0.4110   -0.7184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5305    0.2684   -0.9793 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9746    1.2990   -1.9453 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8368    1.3672   -3.0255 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3427    0.7459   -2.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3380    0.5703   -1.3291 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5724   -0.1288   -1.7532 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5575   -1.3024   -2.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    0.6693   -1.8060 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -0.2167   -0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6113   -0.9451    3.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7579    0.4357    3.3350 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3980    0.6106    4.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4439    1.5881    0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5910   -0.3069    1.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3737    1.3872    1.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.0328   -0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6010   -1.9322    0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8628   -2.0003   -0.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2601    0.4996    2.1758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6868    0.4417    2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5651    2.0019    1.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1858    1.4243   -0.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1803    2.3866    0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2495    1.1618    1.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2317   -0.9406    2.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8615   -1.6957   -0.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4594   -2.4271    0.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6251   -0.7702    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2953    1.3848   -1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235   -0.3526   -1.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3311   -0.7228   -1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8213    2.2549   -1.4370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4631    2.1276   -2.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7607    1.5026   -3.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1300   -0.1520   -3.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6380    1.6172   -1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676   -1.7138   -2.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036   -1.0049   -3.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2018   -2.1269   -2.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8115    1.7718   -1.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6675    0.3539   -2.4991 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1928   -1.1223   -0.5509 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  0
 20 19  1  0
 19 18  1  0
 18 12  1  0
 12 13  1  6
 12 11  1  0
 11 10  1  0
 10  9  2  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 23 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  0
 27  5  1  0
  9  7  1  0
 27 24  1  0
  9 19  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  5 31  1  6
  6 32  1  0
  6 33  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
 23 54  1  1
 22 52  1  0
 22 53  1  0
 20 50  1  1
 21 51  1  0
 19 49  1  6
 18 47  1  0
 18 48  1  0
 13 40  1  0
 13 41  1  0
 13 42  1  0
 11 38  1  0
 11 39  1  0
 10 37  1  0
 14 43  1  1
 16 44  1  0
 16 45  1  0
 17 46  1  0
 25 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  0
 26 59  1  0
 27 60  1  1
M  END


  Mrv1652309102218282D          

 27 30  0  0  1  0            999 V2000
    0.3402   -0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6464   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1361   -1.5321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4630   -1.0018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7692   -1.7679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5857   -1.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8919   -2.6518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4022   -2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2188   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0353   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3415   -3.0054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0428   -2.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8913   -3.6205    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6989   -3.4520    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.6334   -4.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1832   -5.0193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8312   -3.6536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0146   -3.5357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5043   -4.1839    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8105   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6878   -4.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5650   -3.1821    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4472   -3.9987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485   -3.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2588   -2.4161    0.0000 C   0  0  1  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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 19 18  1  1  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 23 22  1  6  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 27 26  1  1  0  0  0
  5 27  1  0  0  0  0
 24 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302715

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@]2(C)[C@H](C[C@@H](O)[C@@H]3C[C@](C)(CC=C23)[C@H](Br)CO)[C@@]2(C)C[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C22H33BrO4/c1-12(25)27-17-10-22(4)14-5-6-20(2,19(23)11-24)8-13(14)16(26)7-18(22)21(3)9-15(17)21/h5,13,15-19,24,26H,6-11H2,1-4H3/t13-,15+,16-,17-,18-,19-,20+,21+,22+/m1/s1

> <INCHI_KEY>
UVYAPBDOYMZESV-QCLOFMSXSA-N

> <FORMULA>
C22H33BrO4

> <MOLECULAR_WEIGHT>
441.406

> <EXACT_MASS>
440.156223

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.24983701809137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-14-yl acetate

> <JCHEM_LOGP>
2.5662126663333344

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.577698461361084

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.50579317910642

> <JCHEM_PKA_STRONGEST_BASIC>
-0.796514423220812

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
108.22609999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.635  -0.220   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.207  -1.650   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.254  -2.860   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.731  -1.870   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.302  -3.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.827  -3.520   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.398  -4.950   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.351  -3.740   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.922  -5.170   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.875  -3.960   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.399  -4.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.971  -5.610   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.280  -4.799   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.997  -6.758   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0      12.505  -6.444   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0      10.516  -8.221   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.542  -9.369   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.018  -6.820   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.494  -6.600   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.541  -7.810   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.113  -9.240   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.017  -7.590   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.446  -6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.921  -5.940   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.701  -7.464   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.397  -5.720   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.350  -4.510   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   27                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   23                                             
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   18                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   12   19                                                       
CONECT   19   18    9   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22    7   24                                                  
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26    5   24                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-Bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0,.0,]pentadec-2-en-14-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₃BrO₄

Average Mass

441.4060 Da

Monoisotopic Mass

440.15622 Da

IUPAC Name

(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-14-yl acetate

Traditional Name

(1R,5S,7R,8R,10R,11R,13R,14R)-5-[(1S)-1-bromo-2-hydroxyethyl]-8-hydroxy-1,5,11-trimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-14-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@]2(C)[C@H](C[C@@H](O)[C@@H]3C[C@](C)(CC=C23)[C@H](Br)CO)[C@@]2(C)C[C@@H]12

InChI Identifier

InChI=1S/C22H33BrO4/c1-12(25)27-17-10-22(4)14-5-6-20(2,19(23)11-24)8-13(14)16(26)7-18(22)21(3)9-15(17)21/h5,13,15-19,24,26H,6-11H2,1-4H3/t13-,15+,16-,17-,18-,19-,20+,21+,22+/m1/s1

InChI Key

UVYAPBDOYMZESV-QCLOFMSXSA-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
Laurencia saitoi	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
Cyclic alcohol
Bromohydrin
Carboxylic acid ester
Secondary alcohol
Halohydrin
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alcohol
Organohalogen compound
Organobromide
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Alkyl halide
Alkyl bromide
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	2.57	ChemAxon
pKa (Strongest Acidic)	14.51	ChemAxon
pKa (Strongest Basic)	-0.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.23 m³·mol⁻¹	ChemAxon
Polarizability	45.25 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

163014012

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate (NP0302715)

MOL for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D MOL for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D SDF for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D-SDF for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

PDB for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D PDB for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

SMILES for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

INCHI for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

Structure for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)

3D Structure for NP0302715 ((1ar,1br,3r,3ar,5s,7br,9r,9ar)-5-[(1s)-1-bromo-2-hydroxyethyl]-3-hydroxy-1a,5,7b-trimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-9-yl acetate)