NP-MRD: Showing NP-Card for 23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione (NP0263866)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 07:11:06 UTC

Updated at

2022-09-08 07:11:06 UTC

NP-MRD ID

NP0263866

Secondary Accession Numbers

None

Natural Product Identification

Common Name

23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione

Description

23'-Acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]Octacosane]-1',9',19'-triene-3',18'-dione belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain. 23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione is found in Paramyrothecium roridum. Based on a literature review very few articles have been published on 23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]Octacosane]-1',9',19'-triene-3',18'-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082209112D          

 39 44  0  0  0  0            999 V2000
   11.1381   -2.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0682   -1.3758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7451   -0.9043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3213   -1.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3343   -1.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1302   -2.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6101   -3.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8612   -3.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0301   -3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6274   -4.3704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5329   -2.9727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0106   -2.3035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3648   -2.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5923   -2.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.9178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949   -1.0080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5647   -0.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7153    0.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0863    0.9045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3095    0.6267    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0997    0.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0462   -0.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8580   -0.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    0.2510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9162    0.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7249    1.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7041    0.5759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4236    0.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0945    0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8647    0.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9749   -0.4990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5510   -0.6972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8993   -1.2031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6248   -1.4983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3232   -1.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0644   -1.9639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2436   -1.8801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7266   -1.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 28 26  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 32  1  0  0  0  0
 29 33  1  0  0  0  0
  4 33  1  0  0  0  0
 33 34  1  0  0  0  0
 23 35  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 14 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 39  1  0  0  0  0
M  END

     RDKit          3D

 75 80  0  0  0  0  0  0  0  0999 V2000
    3.8621    0.4133    2.4204 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5437    0.6135    1.1129 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6474    1.1422    1.1357 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9943    0.2281   -0.1788 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8555   -1.3020   -0.1709 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5347   -1.7445    0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4728   -3.1429    0.8176 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7125   -4.0886    0.2920 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873   -3.9413   -0.2745 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2483   -4.4362   -1.4586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7186   -3.3717    0.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0506   -2.1380    0.7531 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6298   -2.4002    2.1566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9429   -1.6024    2.1417 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5543   -0.2616    2.2624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9422    0.3968    1.1284 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9578    1.8604    1.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1598    2.5249    0.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1882    4.0273    0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4654    4.3838   -0.4114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3620    1.8695   -1.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0109    0.4272   -1.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1828   -0.0368   -0.1128 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8056    0.5262   -0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6654    1.7414   -0.8128 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2363    2.4187   -1.5590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1671    2.7257   -2.7598 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5757    2.8651   -1.2500 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6381    2.1953   -0.8786 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0095    2.8367   -0.7705 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0738    1.9433   -1.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8642    0.5986   -1.1973 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    0.7560   -0.5289 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2900    0.1210   -1.7384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1912   -1.5634   -0.0661 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2145   -2.1526   -1.4594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3956   -1.9475    0.7403 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6756   -2.2685    0.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7677   -3.2864    0.6135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8106    0.7896    2.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3632    1.0136    3.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8468   -0.6150    2.7712 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6660   -1.7666    0.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9358   -1.6212   -1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -1.1513    1.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7163   -1.6809   -0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1241   -3.3801    1.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1920   -5.0883    0.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2514   -1.4244    0.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9624   -2.0914    2.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9135   -3.4443    2.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6279   -1.9305    2.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0113    0.0806    0.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8206    2.4388    2.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3962    4.4435   -0.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1560    4.3850    1.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6447    4.0442   -1.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8000    2.4812   -2.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4385    2.0225   -1.5171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512   -0.1610   -1.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4860    0.2190   -2.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2065   -0.2845   -0.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3995    0.5999    0.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7980    3.9592   -1.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1789    3.2560    0.2388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9297    3.7493   -1.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0514    2.2521   -0.8640 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1961    2.1602   -2.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9361    0.6324    0.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9259    0.4822   -2.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3611   -1.7897   -2.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2331   -3.2618   -1.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1349   -1.8881   -1.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5458   -2.1163    1.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9989   -2.2437   -0.7127 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  4  2  1  1
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 23 22  1  6
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 29 33  1  0
 33 34  1  0
 23 35  1  0
 35 36  1  6
 35 37  1  0
 37 38  1  0
 38 39  1  0
 32  4  1  0
 37 39  1  1
 33  4  1  0
 35 12  1  0
 37 14  1  0
 23 16  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  6 46  1  0
  7 47  1  0
  8 48  1  0
 12 49  1  1
 13 50  1  0
 13 51  1  0
 14 52  1  1
 16 53  1  6
 17 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  0
 21 58  1  0
 21 59  1  0
 22 60  1  0
 22 61  1  0
 24 62  1  0
 24 63  1  0
 28 64  1  0
 30 65  1  0
 30 66  1  0
 31 67  1  0
 31 68  1  0
 33 69  1  1
 34 70  1  0
 36 71  1  0
 36 72  1  0
 36 73  1  0
 38 74  1  0
 38 75  1  0
M  END


  Mrv1652309082209112D          

 39 44  0  0  0  0            999 V2000
   11.1381   -2.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0682   -1.3758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7451   -0.9043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3213   -1.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3343   -1.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1302   -2.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6101   -3.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8612   -3.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0301   -3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6274   -4.3704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5329   -2.9727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0106   -2.3035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3648   -2.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5923   -2.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.9178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949   -1.0080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5647   -0.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7153    0.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0863    0.9045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3095    0.6267    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0997    0.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0462   -0.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8580   -0.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    0.2510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9162    0.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7249    1.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7041    0.5759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4236    0.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0945    0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8647    0.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9749   -0.4990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5510   -0.6972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8993   -1.2031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6248   -1.4983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3232   -1.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0644   -1.9639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2436   -1.8801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7266   -1.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 28 26  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 32  1  0  0  0  0
 29 33  1  0  0  0  0
  4 33  1  0  0  0  0
 33 34  1  0  0  0  0
 23 35  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 14 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263866

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C12CCC=CC(=O)OC3CC4OC5C=C(CO)CCC5(COC(=O)C=C(CCO1)C2O)C3(C)C41CO1

> <INCHI_IDENTIFIER>
InChI=1S/C29H36O10/c1-17(31)28-8-4-3-5-23(32)39-20-13-22-29(16-37-29)26(20,2)27(9-6-18(14-30)11-21(27)38-22)15-35-24(33)12-19(25(28)34)7-10-36-28/h3,5,11-12,20-22,25,30,34H,4,6-10,13-16H2,1-2H3

> <INCHI_KEY>
FAUFOECCTCIGCY-UHFFFAOYSA-N

> <FORMULA>
C29H36O10

> <MOLECULAR_WEIGHT>
544.597

> <EXACT_MASS>
544.230847359

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.16765342180021

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19'-triene-3',18'-dione

> <JCHEM_LOGP>
1.1074534253333317

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.077403577035323

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.17021031096699

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7344927114403603

> <JCHEM_POLAR_SURFACE_AREA>
141.12000000000003

> <JCHEM_REFRACTIVITY>
137.6736

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19'-triene-3',18'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      20.791  -4.103   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.661  -2.568   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      21.924  -1.688   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      19.266  -1.914   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.291  -3.499   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.910  -5.014   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.939  -6.236   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.541  -6.942   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.990  -6.814   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      14.238  -8.158   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      14.061  -5.549   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      13.087  -4.300   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.881  -5.402   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.439  -4.654   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.128  -3.580   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.697  -1.882   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.521  -0.833   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.802   0.692   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.628   1.688   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.178   1.170   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.247   1.213   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.386   0.159   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.286  -1.450   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.802  -0.825   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.698   0.468   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      14.777   1.587   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      14.420   3.085   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      16.248   1.075   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      17.591   0.250   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      18.843   1.187   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      20.281   0.609   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      20.486  -0.931   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      17.828  -1.301   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      16.612  -2.246   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      12.366  -2.797   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.670  -1.977   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      11.320  -3.666   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.788  -3.509   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      10.690  -2.261   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   32   33                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   35                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   37                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16   24   35                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   33                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    4                                                       
CONECT   33   29    4   34                                                  
CONECT   34   33                                                            
CONECT   35   23   12   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   14   38   39                                             
CONECT   38   37   39                                                       
CONECT   39   38   37                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   88    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₆O₁₀

Average Mass

544.5970 Da

Monoisotopic Mass

544.23085 Da

IUPAC Name

23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19'-triene-3',18'-dione

Traditional Name

23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19'-triene-3',18'-dione

CAS Registry Number

Not Available

SMILES

CC(=O)C12CCC=CC(=O)OC3CC4OC5C=C(CO)CCC5(COC(=O)C=C(CCO1)C2O)C3(C)C41CO1

InChI Identifier

InChI=1S/C29H36O10/c1-17(31)28-8-4-3-5-23(32)39-20-13-22-29(16-37-29)26(20,2)27(9-6-18(14-30)11-21(27)38-22)15-35-24(33)12-19(25(28)34)7-10-36-28/h3,5,11-12,20-22,25,30,34H,4,6-10,13-16H2,1-2H3

InChI Key

FAUFOECCTCIGCY-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Myrothecium roridum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Trichothecenes

Alternative Parents

Substituents

Trichothecene skeleton
Macrolide
Oxepane
Oxane
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	1.11	ChemAxon
pKa (Strongest Acidic)	13.17	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	141.12 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	137.67 m³·mol⁻¹	ChemAxon
Polarizability	55.17 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162814254

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione (NP0263866)

MOL for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

3D MOL for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

3D SDF for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

3D-SDF for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

PDB for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

3D PDB for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

SMILES for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

INCHI for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

Structure for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)

3D Structure for NP0263866 (23'-acetyl-27'-hydroxy-9'-(hydroxymethyl)-15'-methyl-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19'-triene-3',18'-dione)