NP-MRD: Showing NP-Card for Persicamidine C (NP0333158)

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Record Information

Version

2.0

Created at

2024-05-11 19:32:56 UTC

Updated at

2024-09-03 04:21:22 UTC

NP-MRD ID

NP0333158

Natural Product DOI

https://doi.org/10.57994/2463

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Persicamidine C

Description

Persicamidine C belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions. Persicamidine C was first documented in 2023 (PMID: 36422061). Based on a literature review very few articles have been published on Persicamidine C.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01232322092D          

 59 67  0  0  1  0            999 V2000
   11.5500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7250    0.2211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3125   -0.4934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7250   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0750    0.2211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8375    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8375    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6127    2.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7560    3.4591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6942    3.1769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9500    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7125    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1250    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0625    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6500    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6500    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.0789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    3.0789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4750    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6000    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  4  3  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  3  9  1  0  0  0  0
 10  9  1  0  0  0  0
 10  8  1  0  0  0  0
 10 11  1  1  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 14 17  1  6  0  0  0
 18 14  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 26 25  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 21  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 31 30  1  6  0  0  0
 32 31  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 39  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 38 45  2  0  0  0  0
 46 45  1  0  0  0  0
 46 35  1  0  0  0  0
 46 47  1  1  0  0  0
 48 46  1  0  0  0  0
 48 49  1  1  0  0  0
 50 48  1  0  0  0  0
 32 50  1  0  0  0  0
 50 51  1  6  0  0  0
 32 51  1  6  0  0  0
 31 52  1  0  0  0  0
 52 26  1  0  0  0  0
 52 53  1  1  0  0  0
 53 54  1  0  0  0  0
 33 54  1  0  0  0  0
 54 55  2  0  0  0  0
 56 18  1  0  0  0  0
 23 56  1  0  0  0  0
 56 57  1  1  0  0  0
 56 58  1  0  0  0  0
 58 12  1  0  0  0  0
 58 59  1  1  0  0  0
M  END


  Mrv2104 01232322092D          

 59 67  0  0  1  0            999 V2000
   11.5500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7250    0.2211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3125   -0.4934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7250   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0750    0.2211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8375    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8375    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6127    2.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7560    3.4591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6942    3.1769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9500    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7125    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1250    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0625    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6500    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6500    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.0789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    3.0789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4750    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6000    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  4  3  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  3  9  1  0  0  0  0
 10  9  1  0  0  0  0
 10  8  1  0  0  0  0
 10 11  1  1  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 14 17  1  6  0  0  0
 18 14  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 20  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 26 25  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 21  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 31 30  1  6  0  0  0
 32 31  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 39  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 38 45  2  0  0  0  0
 46 45  1  0  0  0  0
 46 35  1  0  0  0  0
 46 47  1  1  0  0  0
 48 46  1  0  0  0  0
 48 49  1  1  0  0  0
 50 48  1  0  0  0  0
 32 50  1  0  0  0  0
 50 51  1  6  0  0  0
 32 51  1  6  0  0  0
 31 52  1  0  0  0  0
 52 26  1  0  0  0  0
 52 53  1  1  0  0  0
 53 54  1  0  0  0  0
 33 54  1  0  0  0  0
 54 55  2  0  0  0  0
 56 18  1  0  0  0  0
 23 56  1  0  0  0  0
 56 57  1  1  0  0  0
 56 58  1  0  0  0  0
 58 12  1  0  0  0  0
 58 59  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0333158

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@H](O[C@H]2C[C@](C)(CO)[C@@H]3CC[C@@]4(C)[C@@H]5CC[C@@H]6[C@H](CC(=O)[C@]7(C)C8=COC(N[C@H](C)C(C)C)=N[C@]8(C)[C@@H](O)[C@@H]8O[C@]678)[C@@]5(C)CC[C@@H]4[C@@]3(C)[C@@H]2O)O[C@H](C)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H74N2O10/c1-23(2)24(3)48-40-49-46(10)33(21-56-40)45(9)34(51)18-27-26(47(45)39(59-47)38(46)54)12-13-31-42(27,6)16-15-32-43(31,7)17-14-30-41(5,22-50)20-29(37(53)44(30,32)8)58-35-19-28(55-11)36(52)25(4)57-35/h21,23-32,35-39,50,52-54H,12-20,22H2,1-11H3,(H,48,49)/t24-,25-,26-,27+,28-,29+,30+,31-,32+,35+,36-,37-,38+,39+,41-,42-,43+,44+,45+,46+,47+/m1/s1

> <INCHI_KEY>
NWFBSKMPTYKHMN-FTFYICBJSA-N

> <FORMULA>
C47H74N2O10

> <MOLECULAR_WEIGHT>
827.113

> <EXACT_MASS>
826.534346591

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
133

> <JCHEM_AVERAGE_POLARIZABILITY>
95.76560603190708

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,6R,7S,8S,10S,11S,14S,15R,18R,19R,21S,22R,23S,29R)-7,22-dihydroxy-8-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-10-(hydroxymethyl)-2,6,10,14,23,29-hexamethyl-25-{[(2R)-3-methylbutan-2-yl]amino}-20,26-dioxa-24-azaoctacyclo[16.13.0.0^{2,15}.0^{5,14}.0^{6,11}.0^{19,21}.0^{19,29}.0^{23,28}]hentriaconta-24,27-dien-30-one

> <JCHEM_LOGP>
4.9538591506666645

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.29658951166044

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.751459863376432

> <JCHEM_PKA_STRONGEST_BASIC>
5.120954575961536

> <JCHEM_POLAR_SURFACE_AREA>
171.82999999999998

> <JCHEM_REFRACTIVITY>
219.13290000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,6R,7S,8S,10S,11S,14S,15R,18R,19R,21S,22R,23S,29R)-7,22-dihydroxy-8-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-10-(hydroxymethyl)-2,6,10,14,23,29-hexamethyl-25-{[(2R)-3-methylbutan-2-yl]amino}-20,26-dioxa-24-azaoctacyclo[16.13.0.0^{2,15}.0^{5,14}.0^{6,11}.0^{19,21}.0^{19,29}.0^{23,28}]hentriaconta-24,27-dien-30-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-JAN-23         0                                  
HETATM    1  C   UNK     0      21.560   3.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      20.020   3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      19.250   1.746   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.020   0.413   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      21.560   0.413   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      19.250  -0.921   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.020  -2.255   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      17.710  -0.921   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      17.710   1.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.940   0.413   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      15.400   0.413   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      14.630   1.746   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.400   3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.630   4.414   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.077   4.940   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.345   6.457   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      14.363   5.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.090   4.414   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.320   5.747   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.780   5.747   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.010   4.414   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.240   5.747   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.780   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.010   1.746   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.470   1.746   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.700   3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.930   1.746   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.470   4.414   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.700   5.747   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.160   5.747   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.390   4.414   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.850   4.414   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.080   3.080   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.310   1.746   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.540   3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.770   1.746   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.770   1.746   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.540   3.080   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0      -3.080   3.080   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0      -3.850   1.746   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.080   0.413   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -5.390   1.746   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -6.160   0.413   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -6.160   3.080   0.000  0.00  0.00           C+0
HETATM   45  N   UNK     0      -0.770   4.414   0.000  0.00  0.00           N+0
HETATM   46  C   UNK     0       0.770   4.414   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -0.000   5.747   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.540   5.747   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       0.770   7.081   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       3.080   5.747   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       4.620   5.747   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       6.160   3.080   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       5.390   1.746   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       3.850   1.746   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       3.080   0.413   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      12.320   3.080   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      11.550   1.746   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      13.090   1.746   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      12.320   0.413   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6   10                                                       
CONECT    9    3   10                                                       
CONECT   10    9    8   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   58                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17   18                                             
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14                                                            
CONECT   18   14   19   56                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   28                                             
CONECT   22   21                                                            
CONECT   23   21   24   56                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   52                                             
CONECT   27   26                                                            
CONECT   28   26   21   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   52                                                  
CONECT   32   31   33   50   51                                             
CONECT   33   32   34   35   54                                             
CONECT   34   33                                                            
CONECT   35   33   36   46                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   45                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   38   46                                                       
CONECT   46   45   35   47   48                                             
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   32   51                                                  
CONECT   51   50   32                                                       
CONECT   52   31   26   53                                                  
CONECT   53   52   54                                                       
CONECT   54   53   33   55                                                  
CONECT   55   54                                                            
CONECT   56   18   23   57   58                                             
CONECT   57   56                                                            
CONECT   58   56   12   59                                                  
CONECT   59   58                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  134    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₇H₇₄N₂O₁₀

Average Mass

827.1130 Da

Monoisotopic Mass

826.53435 Da

IUPAC Name

(1S,2R,5S,6R,7S,8S,10S,11S,14S,15R,18R,19R,21S,22R,23S,29R)-7,22-dihydroxy-8-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-10-(hydroxymethyl)-2,6,10,14,23,29-hexamethyl-25-{[(2R)-3-methylbutan-2-yl]amino}-20,26-dioxa-24-azaoctacyclo[16.13.0.0^{2,15}.0^{5,14}.0^{6,11}.0^{19,21}.0^{19,29}.0^{23,28}]hentriaconta-24,27-dien-30-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@H](O[C@H]2C[C@](C)(CO)[C@@H]3CC[C@@]4(C)[C@@H]5CC[C@@H]6[C@H](CC(=O)[C@]7(C)C8=COC(N[C@H](C)C(C)C)=N[C@]8(C)[C@@H](O)[C@@H]8O[C@]678)[C@@]5(C)CC[C@@H]4[C@@]3(C)[C@@H]2O)O[C@H](C)[C@H]1O

InChI Identifier

InChI=1S/C47H74N2O10/c1-23(2)24(3)48-40-49-46(10)33(21-56-40)45(9)34(51)18-27-26(47(45)39(59-47)38(46)54)12-13-31-42(27,6)16-15-32-43(31,7)17-14-30-41(5,22-50)20-29(37(53)44(30,32)8)58-35-19-28(55-11)36(52)25(4)57-35/h21,23-32,35-39,50,52-54H,12-20,22H2,1-11H3,(H,48,49)/t24-,25-,26-,27+,28-,29+,30+,31-,32+,35+,36-,37-,38+,39+,41-,42-,43+,44+,45+,46+,47+/m1/s1

InChI Key

NWFBSKMPTYKHMN-FTFYICBJSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
MLEV NMR	[¹H, ¹H] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD3OD, experimental)	amninder.kaur@helmholtz-hips.de	Not Available	Not Available	2024-05-11	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Kibdelosporangium persicum		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Scalarane sesterterpenoids

Alternative Parents

Substituents

Scalarane sesterterpenoid
Terpene glycoside
Oxepane
Oxane
Monosaccharide
Meta-oxazine
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Ether
Oxirane
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	4.95	ChemAxon
pKa (Strongest Acidic)	12.75	ChemAxon
pKa (Strongest Basic)	5.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	171.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	219.13 m³·mol⁻¹	ChemAxon
Polarizability	95.77 Å³	ChemAxon
Number of Rings	9	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Keller L, Oueis E, Kaur A, Safaei N, Kirsch SH, Gunesch AP, Haid S, Rand U, Cicin-Sain L, Fu C, Wink J, Pietschmann T, Muller R: Persicamidines-Unprecedented Sesquarterpenoids with Potent Antiviral Bioactivity against Coronaviruses. Angew Chem Int Ed Engl. 2023 Feb 1;62(6):e202214595. doi: 10.1002/anie.202214595. Epub 2023 Jan 4. [PubMed:36422061 ]
DOI: 10.1002/anie.202214595

Showing NP-Card for Persicamidine C (NP0333158)

MOL for NP0333158 (Persicamidine C)

3D MOL for NP0333158 (Persicamidine C)

3D SDF for NP0333158 (Persicamidine C)

3D-SDF for NP0333158 (Persicamidine C)

PDB for NP0333158 (Persicamidine C)

3D PDB for NP0333158 (Persicamidine C)

SMILES for NP0333158 (Persicamidine C)

INCHI for NP0333158 (Persicamidine C)

Structure for NP0333158 (Persicamidine C)

3D Structure for NP0333158 (Persicamidine C)