NP-MRD: Showing NP-Card for Curvularol (NP0003633)

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Record Information

Version

2.0

Created at

2020-12-09 00:49:40 UTC

Updated at

2021-07-15 16:46:57 UTC

NP-MRD ID

NP0003633

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Curvularol

Provided By

NPAtlas

Description

Curvularol belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. Curvularol is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Curvularol is found in Curvularia. Curvularol was first documented in 2001 (PMID: 11269706). Based on a literature review very few articles have been published on curvularol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117483D          

 41 44  0  0  0  0            999 V2000
    3.7253    0.2593    2.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5063    0.2495    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3113    0.4647    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.4591    1.1095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9531   -0.1566    1.7908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118   -0.1393    1.0278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1528   -0.5853    1.8037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3634    1.1938    0.3730 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5253    1.1578   -0.8677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0899    2.3387   -1.4880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2079    1.6012   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2097   -0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7490   -0.6915   -2.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9786   -1.0328   -0.2146 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1723   -0.9705   -0.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398   -0.3402   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5386   -1.7953    0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    0.0712   -0.8926 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7609   -0.0068    0.0026 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3928    1.0603    1.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4437    0.5139    3.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2617   -0.6979    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.6441    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794    1.5140    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0817   -1.5918    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    1.1873    0.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    2.0477    1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4359    3.3210   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    2.4477   -2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -1.5300   -2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143   -0.9130   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3024    0.1579   -2.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -2.0302    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7443   -1.7374   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -1.9978    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2985   -2.5035   -0.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.9250    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5102    1.0312   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -0.7005   -1.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4844    0.7940   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3511   -0.9591   -0.1421 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  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
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19  2  1  0  0  0  0
 16  4  1  0  0  0  0
 14  6  1  0  0  0  0
  9 11  1  6  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  6  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
 13 30  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 14 33  1  1  0  0  0
 15 34  1  0  0  0  0
 17 35  1  0  0  0  0
 17 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 19 40  1  0  0  0  0
 19 41  1  0  0  0  0
M  END

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
    3.7253    0.2593    2.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5063    0.2495    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3113    0.4647    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.4591    1.1095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9531   -0.1566    1.7908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118   -0.1393    1.0278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1528   -0.5853    1.8037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3634    1.1938    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5253    1.1578   -0.8677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0899    2.3387   -1.4880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2079    1.6012   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2097   -0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7490   -0.6915   -2.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9786   -1.0328   -0.2146 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1723   -0.9705   -0.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398   -0.3402   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5386   -1.7953    0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    0.0712   -0.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -0.0068    0.0026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928    1.0603    1.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4437    0.5139    3.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2617   -0.6979    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.6441    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794    1.5140    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0817   -1.5918    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    1.1873    0.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    2.0477    1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4359    3.3210   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    2.4477   -2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -1.5300   -2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143   -0.9130   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3024    0.1579   -2.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -2.0302    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7443   -1.7374   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -1.9978    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2985   -2.5035   -0.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.9250    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5102    1.0312   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -0.7005   -1.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4844    0.7940   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3511   -0.9591   -0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19  2  1  0
 16  4  1  0
 14  6  1  0
  9 11  1  6
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  6
  7 25  1  0
  8 26  1  0
  8 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
 14 33  1  1
 15 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 19 41  1  0
M  END


  Mrv1652306242117483D          

 41 44  0  0  0  0            999 V2000
    3.7253    0.2593    2.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5063    0.2495    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3113    0.4647    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.4591    1.1095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9531   -0.1566    1.7908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118   -0.1393    1.0278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1528   -0.5853    1.8037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3634    1.1938    0.3730 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5253    1.1578   -0.8677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0899    2.3387   -1.4880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2079    1.6012   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2097   -0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7490   -0.6915   -2.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9786   -1.0328   -0.2146 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1723   -0.9705   -0.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398   -0.3402   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5386   -1.7953    0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    0.0712   -0.8926 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7609   -0.0068    0.0026 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3928    1.0603    1.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4437    0.5139    3.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2617   -0.6979    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.6441    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794    1.5140    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0817   -1.5918    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    1.1873    0.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    2.0477    1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4359    3.3210   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    2.4477   -2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -1.5300   -2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143   -0.9130   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3024    0.1579   -2.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -2.0302    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7443   -1.7374   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -1.9978    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2985   -2.5035   -0.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.9250    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5102    1.0312   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -0.7005   -1.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4844    0.7940   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3511   -0.9591   -0.1421 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  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
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19  2  1  0  0  0  0
 16  4  1  0  0  0  0
 14  6  1  0  0  0  0
  9 11  1  6  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  6  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
 10 28  1  0  0  0  0
 10 29  1  0  0  0  0
 13 30  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 14 33  1  1  0  0  0
 15 34  1  0  0  0  0
 17 35  1  0  0  0  0
 17 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 19 40  1  0  0  0  0
 19 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003633

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])[C@@]2(O[H])O[C@@]3([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])[C@]3(C([H])([H])[H])[C@]1(C([H])([H])[H])[C@@]1(OC1([H])[H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O4/c1-9-4-5-12(2)10(6-9)19-15(17)7-14(8-18-14)13(12,3)11(15)16/h6,10-11,16-17H,4-5,7-8H2,1-3H3/t10-,11-,12-,13+,14+,15-/m0/s1

> <INCHI_KEY>
SSTQGEBHEZQSQQ-HCKLQLJTSA-N

> <FORMULA>
C15H22O4

> <MOLECULAR_WEIGHT>
266.337

> <EXACT_MASS>
266.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.156552228287993

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,2'R,7'S,9'S,12'S)-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-9',12'-diol

> <ALOGPS_LOGP>
0.74

> <JCHEM_LOGP>
1.4864739626666659

> <ALOGPS_LOGS>
-1.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.592218269408473

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.995542524407023

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7695700447044844

> <JCHEM_POLAR_SURFACE_AREA>
62.22

> <JCHEM_REFRACTIVITY>
68.9786

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.71e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,2'R,7'S,9'S,12'S)-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-9',12'-diol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
    3.7253    0.2593    2.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5063    0.2495    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3113    0.4647    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.4591    1.1095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9531   -0.1566    1.7908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118   -0.1393    1.0278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1528   -0.5853    1.8037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3634    1.1938    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5253    1.1578   -0.8677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0899    2.3387   -1.4880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2079    1.6012   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2097   -0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7490   -0.6915   -2.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9786   -1.0328   -0.2146 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1723   -0.9705   -0.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398   -0.3402   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5386   -1.7953    0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    0.0712   -0.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -0.0068    0.0026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928    1.0603    1.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4437    0.5139    3.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2617   -0.6979    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.6441    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794    1.5140    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0817   -1.5918    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    1.1873    0.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    2.0477    1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4359    3.3210   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    2.4477   -2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -1.5300   -2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143   -0.9130   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3024    0.1579   -2.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -2.0302    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7443   -1.7374   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -1.9978    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2985   -2.5035   -0.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.9250    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5102    1.0312   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -0.7005   -1.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4844    0.7940   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3511   -0.9591   -0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19  2  1  0
 16  4  1  0
 14  6  1  0
  9 11  1  6
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  6
  7 25  1  0
  8 26  1  0
  8 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
 14 33  1  1
 15 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 19 41  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.725   0.259   2.325  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.506   0.250   1.430  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.311   0.465   1.958  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.123   0.459   1.109  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.953  -0.157   1.791  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.112  -0.139   1.028  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.153  -0.585   1.804  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.363   1.194   0.373  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.525   1.158  -0.868  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.090   2.339  -1.488  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.208   1.601  -2.077  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.923  -0.210  -0.972  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.749  -0.692  -2.376  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.979  -1.033  -0.215  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.172  -0.971  -0.892  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.340  -0.340  -0.143  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.539  -1.795   0.295  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.577   0.071  -0.893  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.761  -0.007   0.003  0.00  0.00           C+0
HETATM   20  H   UNK     0       4.393   1.060   1.926  0.00  0.00           H+0
HETATM   21  H   UNK     0       3.444   0.514   3.354  0.00  0.00           H+0
HETATM   22  H   UNK     0       4.262  -0.698   2.232  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.222   0.644   3.019  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.179   1.514   0.841  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.082  -1.592   1.837  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.448   1.187   0.064  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.151   2.048   1.032  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.436   3.321  -1.107  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.248   2.448  -2.205  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.039  -1.530  -2.370  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.714  -0.913  -2.837  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.302   0.158  -2.961  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.627  -2.030   0.028  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.744  -1.737  -0.627  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.003  -1.998   1.255  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.299  -2.503  -0.501  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.626  -1.925   0.535  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.510   1.031  -1.396  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.721  -0.701  -1.703  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.484   0.794  -0.336  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.351  -0.959  -0.142  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3   19                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5   16   24                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8   14                                             
CONECT    7    6   25                                                       
CONECT    8    6    9   26   27                                             
CONECT    9    8   10   12   11                                             
CONECT   10    9   11   28   29                                             
CONECT   11   10    9                                                       
CONECT   12    9   13   14   16                                             
CONECT   13   12   30   31   32                                             
CONECT   14   12   15    6   33                                             
CONECT   15   14   34                                                       
CONECT   16   12   17   18    4                                             
CONECT   17   16   35   36   37                                             
CONECT   18   16   19   38   39                                             
CONECT   19   18    2   40   41                                             
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28   10                                                            
CONECT   29   10                                                            
CONECT   30   13                                                            
CONECT   31   13                                                            
CONECT   32   13                                                            
CONECT   33   14                                                            
CONECT   34   15                                                            
CONECT   35   17                                                            
CONECT   36   17                                                            
CONECT   37   17                                                            
CONECT   38   18                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   19                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   88    0
END

RDKit          3D

41 44  0  0  0  0  0  0  0  0999 V2000
    3.7253    0.2593    2.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5063    0.2495    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3113    0.4647    1.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.4591    1.1095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9531   -0.1566    1.7908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118   -0.1393    1.0278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1528   -0.5853    1.8037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3634    1.1938    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5253    1.1578   -0.8677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0899    2.3387   -1.4880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2079    1.6012   -2.0769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2097   -0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7490   -0.6915   -2.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9786   -1.0328   -0.2146 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1723   -0.9705   -0.8916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398   -0.3402   -0.1430 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5386   -1.7953    0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    0.0712   -0.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -0.0068    0.0026 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928    1.0603    1.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4437    0.5139    3.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2617   -0.6979    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.6441    3.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794    1.5140    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0817   -1.5918    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    1.1873    0.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    2.0477    1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4359    3.3210   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2475    2.4477   -2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -1.5300   -2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143   -0.9130   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3024    0.1579   -2.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6272   -2.0302    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7443   -1.7374   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -1.9978    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2985   -2.5035   -0.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -1.9250    0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5102    1.0312   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -0.7005   -1.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4844    0.7940   -0.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3511   -0.9591   -0.1421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19  2  1  0
 16  4  1  0
 14  6  1  0
  9 11  1  6
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  6
  7 25  1  0
  8 26  1  0
  8 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
 14 33  1  1
 15 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 19 41  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₄

Average Mass

266.3370 Da

Monoisotopic Mass

266.15181 Da

IUPAC Name

(1'S,2S,2'R,7'S,9'S,12'S)-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-9',12'-diol

Traditional Name

(1'S,2S,2'R,7'S,9'S,12'S)-1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-9',12'-diol

CAS Registry Number

Not Available

SMILES

CC1=C[C@@H]2O[C@@]3(O)C[C@@]4(CO4)[C@](C)(C3O)[C@@]2(C)CC1

InChI Identifier

InChI=1S/C15H22O4/c1-9-4-5-12(2)10(6-9)19-15(17)7-14(8-18-14)13(12,3)11(15)16/h6,10-11,16-17H,4-5,7-8H2,1-3H3/t10-,11?,12-,13+,14+,15-/m0/s1

InChI Key

SSTQGEBHEZQSQQ-HCKLQLJTSA-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
Curvularia	NPAtlas	11269706

Species Where Detected

Species Name	Source	Reference
Curvularia sp. RK97-F166	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
Oxane
Cyclic alcohol
Secondary alcohol
Hemiacetal
Oxacycle
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

organic heterotetracyclic compound (CHEBI:82660 )
epoxide (CHEBI:82660 )
bridged compound (CHEBI:82660 )
cyclic hemiketal (CHEBI:82660 )
oxaspiro compound (CHEBI:82660 )

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	0.74	ALOGPS
logP	1.49	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	11	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.98 m³·mol⁻¹	ChemAxon
Polarizability	28.16 Å³	ChemAxon
Number of Rings	4	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

NPAtlas ID

NPA008851

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00015733

Chemspider ID

7992538

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

82660

Good Scents ID

Not Available

References

General References

Honda Y, Ueki M, Okada G, Onose R, Usami R, Horikoshi K, Osada H: Isolation, and biological properties of a new cell cycle inhibitor, curvularol, isolated from Curvularia sp. RK97-F166. J Antibiot (Tokyo). 2001 Jan;54(1):10-6. doi: 10.7164/antibiotics.54.10. [PubMed:11269706 ]

Showing NP-Card for Curvularol (NP0003633)

MOL for NP0003633 (Curvularol)

3D MOL for NP0003633 (Curvularol)

3D SDF for NP0003633 (Curvularol)

3D-SDF for NP0003633 (Curvularol)

PDB for NP0003633 (Curvularol)

3D PDB for NP0003633 (Curvularol)

SMILES for NP0003633 (Curvularol)

INCHI for NP0003633 (Curvularol)

Structure for NP0003633 (Curvularol)

3D Structure for NP0003633 (Curvularol)