NP-MRD: Showing NP-Card for sesterstatin 1 (NP0257634)

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Record Information

Version

2.0

Created at

2022-09-07 22:48:50 UTC

Updated at

2022-09-07 22:48:50 UTC

NP-MRD ID

NP0257634

Secondary Accession Numbers

None

Natural Product Identification

Common Name

sesterstatin 1

Description

Sesterstatin 1 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. sesterstatin 1 is found in Hyrtios erectus. sesterstatin 1 was first documented in 2012 (PMID: 22926987). Based on a literature review very few articles have been published on sesterstatin 1.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082200482D          

 29 33  0  0  1  0            999 V2000
    0.2565   -2.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0274   -2.5793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1830   -1.7691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -3.2875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2209   -3.2749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0056   -4.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2538   -3.3125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6554   -4.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8523   -2.5919    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2756   -1.8838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1005   -1.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -2.6170    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9254   -1.9089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3270   -2.6295    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7503   -1.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5752   -1.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9768   -2.6546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -3.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0961   -3.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9123   -4.7884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8548   -3.6601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7811   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7286   -3.3502    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1301   -4.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3052   -4.0583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7068   -4.7790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4803   -4.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0788   -3.3251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 19 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
 13 29  1  0  0  0  0
  8 29  1  0  0  0  0
M  END

     RDKit          3D

 67 71  0  0  0  0  0  0  0  0999 V2000
   -3.8570    1.2545    2.1663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5877    0.5567    0.8164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603    1.4619   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2652   -0.7688    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4957   -0.6307    0.2037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5653   -1.9296    0.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0813   -1.8751    0.2590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5879   -0.5125   -0.2739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2091   -0.4032   -1.6190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0823    0.4498    0.7573 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4232    1.7838    0.7452 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608    1.5979    0.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5943    0.7764   -0.1864 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6161    1.6644   -1.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0269    0.4067    0.1579 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8607    1.5128    0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1126    0.9297    1.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3760   -0.4559    0.8417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8549   -1.0509   -0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5125   -2.3158   -0.4355 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2560   -3.1616   -1.3640 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4979   -2.4572    0.5314 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2875   -1.4549    1.4776 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7299   -0.3912   -0.9082 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3741    0.4449   -1.9882 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8869   -1.4581   -1.5293 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3306   -1.6684   -2.8389 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4334   -1.2015   -1.5815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1141   -0.5236   -0.3470 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9356    1.0506    2.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1767    0.8719    2.9373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7992    2.3547    2.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0313    0.9695   -0.7620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4125    1.8314   -0.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6219    2.4016    0.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5904   -1.0333    1.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0526   -0.0064    0.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8109   -2.8694    0.9122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9500   -2.1821   -0.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6142   -2.0712    1.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7272   -2.6401   -0.4624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3171   -0.4741   -1.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9238    0.4405   -2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8825   -1.3248   -2.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7978   -0.0024    1.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7901    2.3233    1.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6757    2.4359   -0.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5040    2.6261    0.8349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2495    1.1654    1.9488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.1724   -2.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2638    2.5477   -1.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3650    2.1434   -1.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -0.3199    1.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    1.9876    1.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0705    2.3314   -0.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1025    0.9486    2.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9782    1.5584    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8119   -1.9220    2.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2609   -0.9936    1.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2755    1.5186   -1.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4853    0.2523   -2.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9901    0.1670   -3.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0620   -2.4437   -1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673   -1.3540   -3.5090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0894   -2.2034   -1.6279 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0725   -0.6612   -2.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2385   -1.1775    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 19 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 10  2  1  0
 29 13  1  0
 29  8  1  0
 24 15  1  0
 23 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  1
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  9 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  1
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  1
 16 54  1  0
 16 55  1  0
 17 56  1  0
 17 57  1  0
 23 58  1  0
 23 59  1  0
 25 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  1
 27 64  1  0
 28 65  1  0
 28 66  1  0
 29 67  1  1
M  END


  Mrv1652309082200482D          

 29 33  0  0  1  0            999 V2000
    0.2565   -2.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0274   -2.5793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1830   -1.7691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -3.2875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2209   -3.2749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0056   -4.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2538   -3.3125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6554   -4.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8523   -2.5919    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2756   -1.8838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1005   -1.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -2.6170    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9254   -1.9089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3270   -2.6295    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7503   -1.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5752   -1.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9768   -2.6546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -3.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0961   -3.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9123   -4.7884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8548   -3.6601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7811   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7286   -3.3502    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1301   -4.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3052   -4.0583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7068   -4.7790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4803   -4.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0788   -3.3251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 19 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
 13 29  1  0  0  0  0
  8 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0257634

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@@]1(C)[C@@H]3CCC4=C(C(=O)OC4)[C@@]3(C)[C@H](O)C[C@H]21

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O4/c1-22(2)15-8-10-24(4)16-7-6-14-13-29-21(28)20(14)25(16,5)19(27)12-17(24)23(15,3)11-9-18(22)26/h15-19,26-27H,6-13H2,1-5H3/t15-,16-,17+,18-,19+,23-,24-,25+/m0/s1

> <INCHI_KEY>
IELITCZHWCOSJX-VAWUUXLBSA-N

> <FORMULA>
C25H38O4

> <MOLECULAR_WEIGHT>
402.575

> <EXACT_MASS>
402.277009704

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
46.31275414827608

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,10S,11R,13R,14R,17S,19R)-11,17-dihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-en-8-one

> <JCHEM_LOGP>
3.624873079333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.632375930016217

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.280981240199786

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351214683741061

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
112.25729999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,10S,11R,13R,14R,17S,19R)-11,17-dihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-en-8-one

> <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       0.479  -4.266   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.918  -4.815   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.208  -3.302   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.128  -6.137   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.412  -6.113   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.877  -7.482   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.417  -7.505   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.207  -6.183   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.957  -7.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.458  -4.838   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.248  -3.516   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.788  -3.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.537  -4.885   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.327  -3.563   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.077  -4.908   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.867  -3.587   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.407  -3.610   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.157  -4.955   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.366  -6.277   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.379  -7.437   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.036  -8.938   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.796  -6.832   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.658  -5.298   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.827  -6.254   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.576  -7.599   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.036  -7.575   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.786  -8.921   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.497  -7.552   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.747  -6.207   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   29                                             
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   29                                             
CONECT   14   13                                                            
CONECT   15   13   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   18                                                       
CONECT   24   19   15   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   13    8                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
Sesterstatin-1	MeSH

Chemical Formula

C₂₅H₃₈O₄

Average Mass

402.5750 Da

Monoisotopic Mass

402.27701 Da

IUPAC Name

(1R,2S,10S,11R,13R,14R,17S,19R)-11,17-dihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-en-8-one

Traditional Name

(1R,2S,10S,11R,13R,14R,17S,19R)-11,17-dihydroxy-1,10,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicos-5(9)-en-8-one

CAS Registry Number

Not Available

SMILES

CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@@]1(C)[C@@H]3CCC4=C(C(=O)OC4)[C@@]3(C)[C@H](O)C[C@H]21

InChI Identifier

InChI=1S/C25H38O4/c1-22(2)15-8-10-24(4)16-7-6-14-13-29-21(28)20(14)25(16,5)19(27)12-17(24)23(15,3)11-9-18(22)26/h15-19,26-27H,6-13H2,1-5H3/t15-,16-,17+,18-,19+,23-,24-,25+/m0/s1

InChI Key

IELITCZHWCOSJX-VAWUUXLBSA-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
Hyrtios erectus	LOTUS Database	35616633

Chemical Taxonomy

Description

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
Steroid lactone
Hydroxysteroid
7-hydroxysteroid
16-oxasteroid
Steroid
2-furanone
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

secondary alcohol (CHEBI:66475 )
organic heteropentacyclic compound (CHEBI:66475 )
gamma-lactone (CHEBI:66475 )
terpene lactone (CHEBI:66475 )
scalarane sesterterpenoid (CHEBI:66475 )

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	3.62	ChemAxon
pKa (Strongest Acidic)	13.28	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	112.26 m³·mol⁻¹	ChemAxon
Polarizability	46.31 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9916558

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11741854

PDB ID

Not Available

ChEBI ID

66475

Good Scents ID

Not Available

References

General References

Jimenez T, Morcillo SP, Martin-Lasanta A, Collado-Sanz D, Cardenas DJ, Gansauer A, Justicia J, Cuerva JM: Combining the power of Ti(III)-mediated processes for easy access to hydroxylated polycyclic terpenoids: synthesis of sesterstatin 1 and C-D rings of aspergilloxide. Chemistry. 2012 Oct 1;18(40):12825-33. doi: 10.1002/chem.201201534. Epub 2012 Aug 24. [PubMed:22926987 ]
LOTUS database [Link]

Showing NP-Card for sesterstatin 1 (NP0257634)

MOL for NP0257634 (sesterstatin 1)

3D MOL for NP0257634 (sesterstatin 1)

3D SDF for NP0257634 (sesterstatin 1)

3D-SDF for NP0257634 (sesterstatin 1)

PDB for NP0257634 (sesterstatin 1)

3D PDB for NP0257634 (sesterstatin 1)

SMILES for NP0257634 (sesterstatin 1)

INCHI for NP0257634 (sesterstatin 1)

Structure for NP0257634 (sesterstatin 1)

3D Structure for NP0257634 (sesterstatin 1)