NP-MRD: Showing NP-Card for Taxinine B (NP0074777)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 20:06:12 UTC

Updated at

2022-04-28 20:06:12 UTC

NP-MRD ID

NP0074777

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Taxinine B

Description

Taxinine B 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. Taxinine B is found in Taxus baccata , Taxus canadensis, Taxus cuspidata, Taxus cuspidata Sieb et Zucc , Taxus mairei , Taxus sumatrana , Taxus wallichiana and Taxus yunnanensis. Taxinine B was first documented in 2010 (PMID: 20170941). Based on a literature review very few articles have been published on Taxinine B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222062D          

 48 51  0  0  1  0            999 V2000
    6.9783    1.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1253    1.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9091    0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7935   -0.1960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6609   -0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2763    0.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0808    0.0537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9235   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1955    0.1490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0428    0.9597    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5348    1.6446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3899    1.7449    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5782    2.5482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3679    2.7868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5561    3.5900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9694    2.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1161    2.3555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5224    3.0735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1037    3.7843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3474    3.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643    1.2328    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6385    0.6952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7912   -0.1155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5697   -0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7224   -1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1655   -0.6531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3182   -1.4639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0967   -1.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6924   -2.0015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -2.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2193   -3.3499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3721   -4.1606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -4.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0322   -4.4251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1849   -3.6144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4409   -3.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1116    2.0436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7073    1.7791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804    3.1274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7949    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7467   -1.1164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3561   -1.6725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1424   -1.4228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1792   -2.4783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2308    1.0162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.4155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5332    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  4  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  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 24  1  6  0  0  0
 24 25  2  0  0  0  0
 23 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 21 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 10 41  1  6  0  0  0
  8 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
  3 46  1  0  0  0  0
  3 47  1  0  0  0  0
  1 48  1  0  0  0  0
M  END

     RDKit          3D

 92 95  0  0  0  0  0  0  0  0999 V2000
    1.0484   -2.4131   -1.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9227   -1.4351   -0.3784 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0169   -1.2731    0.6540 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0064   -0.3367    0.2177 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3143   -0.7300   -0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5832   -1.9456    0.1518 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3568    0.2156   -0.4798 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5768   -0.2443   -0.6877 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6976    0.5413   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6273    1.8898   -1.3914 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7037    2.6450   -1.8097 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9144    2.0420   -1.9756 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0268    0.6922   -1.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9402   -0.0401   -1.3042 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4821   -0.9504    1.9913 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382   -0.0362    1.9912 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1945   -0.0602    3.3399 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0513    1.0524    4.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4430    0.9364    5.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6435    2.0716    3.7301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7975   -0.6055    1.0220 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7346   -2.0596    1.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0642    0.0169    1.3426 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0419    1.4379    1.2929 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4068    2.3221    2.2367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3438    3.7962    2.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8278    1.7955    3.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3395   -0.5272    0.7267 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7840   -1.7456    1.2715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8867   -1.9213    2.0553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876   -3.2437    2.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5991   -0.9281    2.3408 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3006   -0.7232   -0.7126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8254    0.4285   -1.1779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8812    1.1686   -0.4164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3233    0.9373   -2.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6322    2.0733   -2.8749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4323    0.0935   -3.2921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251   -0.9589   -2.3835 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8042   -0.1920   -1.5762 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1403    1.2274   -1.5996 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4229    2.1816   -2.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8476    3.5980   -2.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6155    1.8640   -2.8727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1927   -0.4601   -0.3091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9039   -1.6630   -1.7762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9635   -1.8640   -2.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6339   -3.0694   -1.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -2.6747   -2.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9487   -3.0656   -1.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4967   -2.2741    0.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1554    1.2486   -0.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7370   -1.3162   -0.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6891    2.4013   -1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5611    3.7109   -1.9992 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7790    2.6211   -2.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0129    0.2479   -1.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1091   -1.1064   -1.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2615   -0.3561    2.5493 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2996   -1.8348    2.6359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6516    0.9376    1.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5338    0.9300    5.5712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520    1.7264    6.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1056   -0.0558    5.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0316   -2.6512    1.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7112   -2.1010    2.6577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7046   -2.5025    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2829   -0.1319    2.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2979    4.2979    3.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4458    4.0494    1.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2214    4.1152    1.5312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0884    0.2059    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3672   -3.4392    2.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7316   -4.0817    2.1175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1616   -3.3119    3.6914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4250    1.7487   -1.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6909    0.5281   -0.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5140    1.9580    0.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -0.4117   -4.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6527    0.7077   -3.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3074   -1.6654   -3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1239   -0.1506   -2.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5130    3.8855   -3.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0159    4.2999   -2.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4346    3.7969   -1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4509    0.5167   -0.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6926   -2.6740   -2.5330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4587   -2.3347   -3.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5982   -1.0217   -3.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4169   -3.3954   -0.6733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648   -3.2797   -0.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6478   -3.6980   -2.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  2  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  3  2  1  0
  2  1  2  3
  2 45  1  0
 45 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 42 44  2  0
 40 39  1  0
 39 38  1  0
 38 36  1  0
 36 37  2  0
 36 34  1  0
 34 35  1  0
 34 33  2  0
 33 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 28 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 23 21  1  0
 21 22  1  1
 33 46  1  0
 46 47  1  6
 46 48  1  0
 21 16  1  0
 14  9  1  0
 21 45  1  0
 46 39  1  0
 19 62  1  0
 19 63  1  0
 19 64  1  0
 16 61  1  6
 15 59  1  0
 15 60  1  0
  3 51  1  1
  7 52  1  0
  8 53  1  0
 10 54  1  0
 11 55  1  0
 12 56  1  0
 13 57  1  0
 14 58  1  0
  1 49  1  0
  1 50  1  0
 45 86  1  1
 40 82  1  6
 43 83  1  0
 43 84  1  0
 43 85  1  0
 39 81  1  6
 38 79  1  0
 38 80  1  0
 35 76  1  0
 35 77  1  0
 35 78  1  0
 28 72  1  6
 31 73  1  0
 31 74  1  0
 31 75  1  0
 23 68  1  1
 26 69  1  0
 26 70  1  0
 26 71  1  0
 22 65  1  0
 22 66  1  0
 22 67  1  0
 47 87  1  0
 47 88  1  0
 47 89  1  0
 48 90  1  0
 48 91  1  0
 48 92  1  0
M  END


  Mrv1652304282222062D          

 48 51  0  0  1  0            999 V2000
    6.9783    1.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1253    1.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9091    0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7935   -0.1960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6609   -0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2763    0.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0808    0.0537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9235   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1955    0.1490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0428    0.9597    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5348    1.6446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3899    1.7449    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5782    2.5482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3679    2.7868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5561    3.5900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9694    2.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1161    2.3555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5224    3.0735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1037    3.7843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3474    3.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643    1.2328    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6385    0.6952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7912   -0.1155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5697   -0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7224   -1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1655   -0.6531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3182   -1.4639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0967   -1.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6924   -2.0015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -2.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2193   -3.3499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3721   -4.1606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -4.6982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0322   -4.4251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1849   -3.6144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4409   -3.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1116    2.0436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7073    1.7791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804    3.1274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7949    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7467   -1.1164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3561   -1.6725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1424   -1.4228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1792   -2.4783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2308    1.0162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.4155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5332    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  4  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  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 24  1  6  0  0  0
 24 25  2  0  0  0  0
 23 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 21 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 10 41  1  6  0  0  0
  8 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
  3 46  1  0  0  0  0
  3 47  1  0  0  0  0
  1 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074777

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)C(=C)[C@H]2[C@H](OC(C)=O)[C@@H]3CC(=O)C(C)=C([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@]12C)C3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H44O11/c1-19-27(42)17-26-33(45-22(4)39)32-20(2)28(48-30(43)16-15-25-13-11-10-12-14-25)18-29(44-21(3)38)37(32,9)35(47-24(6)41)34(46-23(5)40)31(19)36(26,7)8/h10-16,26,28-29,32-35H,2,17-18H2,1,3-9H3/b16-15+/t26-,28-,29-,32-,33+,34+,35-,37+/m0/s1

> <INCHI_KEY>
SLJNSLIEGINNEE-UWUOQQJISA-N

> <FORMULA>
C37H44O11

> <MOLECULAR_WEIGHT>
664.748

> <EXACT_MASS>
664.288362237

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
69.48208229100638

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,5S,7S,8S,9R,10R)-2,7,9,10-tetrakis(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
3.9912228839999995

> <ALOGPS_LOGS>
-5.69

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.483264535883002

> <JCHEM_PKA_STRONGEST_BASIC>
-5.888193650599053

> <JCHEM_POLAR_SURFACE_AREA>
148.57000000000002

> <JCHEM_REFRACTIVITY>
172.25070000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,5S,7S,8S,9R,10R)-2,7,9,10-tetrakis(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.026   1.940   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.434   2.363   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.030   1.020   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.815  -0.366   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.434  -0.671   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.582   0.441   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      15.084   0.100   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.191  -0.580   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.832   0.278   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.547   1.791   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.465   3.070   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.061   3.257   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.413   4.757   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.887   5.202   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.238   6.701   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      13.010   4.148   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.683   4.397   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.442   5.737   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.660   7.064   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.982   5.751   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.093   2.301   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.925   1.298   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.210  -0.216   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.663  -0.725   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.949  -2.239   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.042  -1.219   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.327  -2.733   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.780  -3.242   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.159  -3.736   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.444  -5.250   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.276  -6.253   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.561  -7.766   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.393  -8.770   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.060  -8.260   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.345  -6.747   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.823  -5.743   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.808   3.815   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.355   4.325   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.187   3.321   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       4.070   5.838   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.084   3.260   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.860  -2.084   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       9.998  -3.122   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      11.466  -2.656   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       9.668  -4.626   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.764   1.897   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.510   0.776   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      14.062   3.080   0.000  0.00  0.00           C+0
CONECT    1    2    6   48                                                  
CONECT    2    1    3   12                                                  
CONECT    3    2    4   46   47                                             
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    4    9   42                                                  
CONECT    9    8   10   24                                                  
CONECT   10    9   11   21   41                                             
CONECT   11   10   12   17                                                  
CONECT   12   11    2   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   10   22   37                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23    9   25                                                  
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   21   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   10                                                            
CONECT   42    8   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46    3                                                            
CONECT   47    3                                                            
CONECT   48    1                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₄O₁₁

Average Mass

664.7480 Da

Monoisotopic Mass

664.28836 Da

IUPAC Name

(1R,2R,3R,5S,7S,8S,9R,10R)-2,7,9,10-tetrakis(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

Traditional Name

(1R,2R,3R,5S,7S,8S,9R,10R)-2,7,9,10-tetrakis(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@H](OC(=O)\C=C\C2=CC=CC=C2)C(=C)[C@H]2[C@H](OC(C)=O)[C@@H]3CC(=O)C(C)=C([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@]12C)C3(C)C

InChI Identifier

InChI=1S/C37H44O11/c1-19-27(42)17-26-33(45-22(4)39)32-20(2)28(48-30(43)16-15-25-13-11-10-12-14-25)18-29(44-21(3)38)37(32,9)35(47-24(6)41)34(46-23(5)40)31(19)36(26,7)8/h10-16,26,28-29,32-35H,2,17-18H2,1,3-9H3/b16-15+/t26-,28-,29-,32-,33+,34+,35-,37+/m0/s1

InChI Key

SLJNSLIEGINNEE-UWUOQQJISA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 baccata	Plant	KNApSAcK
Taxus canadensis	LOTUS Database	35616633
Taxus cuspidata	LOTUS Database	35616633
Taxus cuspidata Sieb et Zucc	Plant	KNApSAcK
Taxus mairei	Plant	KNApSAcK
Taxus sumatrana	Plant	KNApSAcK
Taxus wallichiana	LOTUS Database	35616633
Taxus wallichiana var. yunnanensis	Plant	KNApSAcK

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
Cinnamic acid or derivatives
Cinnamic acid ester
Styrene
Cyclohexenone
Fatty acid ester
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	2.8	ALOGPS
logP	3.99	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	18.48	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	148.57 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	172.25 m³·mol⁻¹	ChemAxon
Polarizability	69.48 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

C00036220

Chemspider ID

8230739

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10055179

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kim SY, Yun-Choi HS: A comparative optical aggregometry study of antiplatelet activity of taxanes from Taxus cuspidata. Thromb Res. 2010 Jun;125(6):e281-4. doi: 10.1016/j.thromres.2009.12.024. Epub 2010 Feb 18. [PubMed:20170941 ]

Showing NP-Card for Taxinine B (NP0074777)

MOL for NP0074777 (Taxinine B)

3D MOL for NP0074777 (Taxinine B)

3D SDF for NP0074777 (Taxinine B)

3D-SDF for NP0074777 (Taxinine B)

PDB for NP0074777 (Taxinine B)

3D PDB for NP0074777 (Taxinine B)

SMILES for NP0074777 (Taxinine B)

INCHI for NP0074777 (Taxinine B)

Structure for NP0074777 (Taxinine B)

3D Structure for NP0074777 (Taxinine B)