NP-MRD: Showing NP-Card for (1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate (NP0168493)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 04:18:48 UTC

Updated at

2022-09-03 04:18:48 UTC

NP-MRD ID

NP0168493

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate

Description

(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]Pentadecan]-11'-en-5'-yl acetate belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system. (1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate is found in Taxus mairei. Based on a literature review very few articles have been published on (1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]Pentadecan]-11'-en-5'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032206182D          

 43 46  0  0  1  0            999 V2000
    7.4137    0.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213    0.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0264    0.1129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4237    1.4855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6312    1.7149    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4337    2.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6412    2.7453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4436    3.5463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0385    4.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410    4.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8310    3.8885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463    2.1737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9397    2.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3105    2.5817    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3919    3.4027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7216    3.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699    3.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029    4.7046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951    2.3217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9898    2.9739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1724    2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603    2.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6671    3.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    1.5825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3670    1.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6038    1.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4459    0.1838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7907   -0.3175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376   -0.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9487    0.3825    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3093   -0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7837    0.6377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2856   -0.0170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9695   -0.7791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4714   -1.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1515   -0.8864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2439    1.3727    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0363    1.1433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6079    0.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    0.3508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5426    1.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386    1.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9601    1.7346    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  1  0  0  0
  5 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 40  1  6  0  0  0
 30 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END

     RDKit          3D

 85 88  0  0  0  0  0  0  0  0999 V2000
    5.7591   -1.4448   -3.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8830   -1.4116   -2.2900 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1483   -2.1808   -1.3305 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8010   -0.5540   -2.2176 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9528   -0.5200   -1.0455 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9574    0.8967   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335    1.4661   -0.4271 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7411    2.6836    0.2437 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4752    3.9105   -0.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197    5.1637    0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0234    3.9402   -1.5092 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6984    0.5247    0.3956 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6215    0.1716    1.5845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4842    1.1137    1.0224 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2917    2.4800    1.3306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3995    2.9788    2.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2291    4.3665    3.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6792    2.1405    3.5525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8409    0.9976    0.3412 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6476    1.8739    1.1335 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0687    3.1215    0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9102    4.0114    1.5531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7415    3.5416   -0.4284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3159   -0.3979    0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0599   -0.5600   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8229    0.5870   -1.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0409   -1.9135   -1.4019 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8275   -1.5810   -2.7719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8774   -2.7683   -0.9940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2187   -2.4674    0.3019 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1162   -3.7042    0.9966 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1719   -1.9517    0.2396 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9130   -2.9849   -0.4471 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8961   -3.7354    0.1520 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5909   -4.7704   -0.6517 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1671   -3.5146    1.3571 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4714   -0.6979   -0.4912 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5697   -0.8439   -1.5445 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4467   -1.4703   -2.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3419   -0.0912   -2.7832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1819   -1.6521    1.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4829   -2.4703    1.1644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7965   -1.5025    2.5678 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7862   -1.5934   -3.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4099   -2.2589   -4.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6635   -0.4499   -3.9836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3937   -1.2638   -0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4033    1.5997   -1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5470    1.1110    0.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1095    1.7277   -1.4143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0581    5.0200    1.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5658    5.7554   -0.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8180    5.8209    0.4155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1917   -0.7251    1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2449    1.0705    1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9517    0.0589    2.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6960    0.6540    2.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8444    4.5608    3.9725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8150    4.5359    3.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4680    5.1082    2.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6872    1.4755   -0.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9397    3.9645    1.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5580    5.0616    1.4013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8789    3.7022    2.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2647    1.2960   -1.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5304    0.1159   -2.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5396    1.0065   -0.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0131   -2.4082   -1.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6817   -1.3376   -3.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1086   -2.7943   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2977   -3.8293   -1.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9475   -3.5735    1.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -1.9682    1.2744 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7111   -5.7142   -0.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5805   -4.4190   -1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608   -5.0499   -1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4071   -0.4891   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5767   -2.0490   -3.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3959   -1.8864   -3.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3129   -1.8047    0.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4006   -3.4175    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7826   -2.7651    2.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2158   -2.4043    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219   -1.5612    2.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3458   -0.6637    3.0349 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  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
  7 12  1  0
 12 13  1  1
 12 37  1  0
 37 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  2  0
 32 30  1  0
 30 31  1  1
 30 29  1  0
 29 27  1  0
 27 28  1  0
 27 25  1  0
 25 26  1  0
 25 24  2  0
 24 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 19 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 24 41  1  0
 41 42  1  0
 41 43  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 38  5  1  0
 38 40  1  6
 14 12  1  0
 41 30  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  5 47  1  1
  6 48  1  0
  6 49  1  0
  7 50  1  6
 10 51  1  0
 10 52  1  0
 10 53  1  0
 13 54  1  0
 13 55  1  0
 13 56  1  0
 37 77  1  6
 32 73  1  1
 35 74  1  0
 35 75  1  0
 35 76  1  0
 31 72  1  0
 29 70  1  0
 29 71  1  0
 27 68  1  6
 28 69  1  0
 26 65  1  0
 26 66  1  0
 26 67  1  0
 19 61  1  6
 22 62  1  0
 22 63  1  0
 22 64  1  0
 14 57  1  1
 17 58  1  0
 17 59  1  0
 17 60  1  0
 42 80  1  0
 42 81  1  0
 42 82  1  0
 43 83  1  0
 43 84  1  0
 43 85  1  0
 39 78  1  0
 39 79  1  0
M  END


  Mrv1652309032206182D          

 43 46  0  0  1  0            999 V2000
    7.4137    0.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213    0.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0264    0.1129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4237    1.4855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6312    1.7149    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4337    2.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6412    2.7453    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4436    3.5463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0385    4.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410    4.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8310    3.8885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463    2.1737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9397    2.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3105    2.5817    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3919    3.4027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7216    3.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699    3.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029    4.7046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951    2.3217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9898    2.9739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1724    2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603    2.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6671    3.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    1.5825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3670    1.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6038    1.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4459    0.1838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7907   -0.3175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376   -0.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9487    0.3825    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3093   -0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7837    0.6377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2856   -0.0170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9695   -0.7791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4714   -1.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1515   -0.8864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2439    1.3727    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0363    1.1433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6079    0.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    0.3508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5426    1.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386    1.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9601    1.7346    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 12 37  1  0  0  0  0
 37 38  1  1  0  0  0
  5 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 40  1  6  0  0  0
 30 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0168493

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H](OC(C)=O)[C@]3(O)C[C@H](O)C(C)=C([C@@H](OC(C)=O)[C@@H]2OC(C)=O)C3(C)C)[C@]11CO1

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O13/c1-13-19(36)11-30(37)26(43-18(6)35)24-28(9,20(39-14(2)31)10-21(40-15(3)32)29(24)12-38-29)25(42-17(5)34)23(41-16(4)33)22(13)27(30,7)8/h19-21,23-26,36-37H,10-12H2,1-9H3/t19-,20-,21-,23+,24-,25-,26-,28+,29-,30+/m0/s1

> <INCHI_KEY>
IPUWXKDQBBTGBE-IVYORAKTSA-N

> <FORMULA>
C30H42O13

> <MOLECULAR_WEIGHT>
610.653

> <EXACT_MASS>
610.262541412

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
60.174929437726504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-7'-yl acetate

> <ALOGPS_LOGP>
1.48

> <JCHEM_LOGP>
-0.8965600616666686

> <ALOGPS_LOGS>
-3.33

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.62491855206131

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.249722480300601

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0188773633399864

> <JCHEM_POLAR_SURFACE_AREA>
184.49

> <JCHEM_REFRACTIVITY>
143.6727

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.86e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-7'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      13.839   0.849   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.360   1.278   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.249   0.211   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.991   2.773   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.512   3.201   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.143   4.696   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.664   5.125   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.295   6.620   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.405   7.687   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.037   9.182   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.885   7.258   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.553   4.058   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.354   5.585   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.180   4.819   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.331   6.352   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.080   7.249   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.677   6.615   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.232   8.782   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.658   4.334   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.714   5.551   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.188   5.343   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.606   3.918   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.245   6.560   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.790   2.954   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.552   1.914   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.127   2.499   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.699   0.343   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.476  -0.593   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.177  -0.210   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.504   0.714   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.177  -0.671   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.063   1.190   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.000  -0.032   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       7.410  -1.454   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.347  -2.676   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       5.883  -1.655   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       7.922   2.562   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.401   2.134   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.468   1.024   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.973   0.655   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.746   1.910   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.232   2.315   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.525   3.238   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   38                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   14   37                                             
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   41                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32   41                                             
CONECT   31   30                                                            
CONECT   32   30   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   12   38                                                  
CONECT   38   37    5   39   40                                             
CONECT   39   38   40                                                       
CONECT   40   39   38                                                       
CONECT   41   30   24   42   43                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Value	Source
(1's,2S,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',7',9',10'-Tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0,]pentadecan]-11'-en-5'-yl acetic acid	Generator

Chemical Formula

C₃₀H₄₂O₁₃

Average Mass

610.6530 Da

Monoisotopic Mass

610.26254 Da

IUPAC Name

(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-7'-yl acetate

Traditional Name

(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-7'-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H](OC(C)=O)[C@]3(O)C[C@H](O)C(C)=C([C@@H](OC(C)=O)[C@@H]2OC(C)=O)C3(C)C)[C@]11CO1

InChI Identifier

InChI=1S/C30H42O13/c1-13-19(36)11-30(37)26(43-18(6)35)24-28(9,20(39-14(2)31)10-21(40-15(3)32)29(24)12-38-29)25(42-17(5)34)23(41-16(4)33)22(13)27(30,7)8/h19-21,23-26,36-37H,10-12H2,1-9H3/t19-,20-,21-,23+,24-,25-,26-,28+,29-,30+/m0/s1

InChI Key

IPUWXKDQBBTGBE-IVYORAKTSA-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
Taxus mairei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Taxanes and derivatives

Alternative Parents

Substituents

Taxane diterpenoid
Pentacarboxylic acid or derivatives
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Alcohol
Carbonyl group
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	1.48	ALOGPS
logP	-0.9	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	13.25	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	184.49 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	143.67 m³·mol⁻¹	ChemAxon
Polarizability	60.17 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

4479399

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5321730

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate (NP0168493)

MOL for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

3D MOL for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

3D SDF for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

3D-SDF for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

PDB for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

3D PDB for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

SMILES for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

INCHI for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

Structure for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)

3D Structure for NP0168493 ((1's,2s,2's,3'r,5's,7's,8's,9'r,10'r,13's)-2',5',9',10'-tetrakis(acetyloxy)-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]pentadecan]-11'-en-7'-yl acetate)