NP-MRD: Showing NP-Card for Botryosphaerin F (NP0011629)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 21:15:26 UTC

Updated at

2021-07-15 17:09:29 UTC

NP-MRD ID

NP0011629

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Botryosphaerin F

Provided By

NPAtlas

Description

(1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadec-2-ene-4,11-dione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Botryosphaerin F is found in Aspergillus. Botryosphaerin F was first documented in 2013 (PMID: 23521163). Based on a literature review very few articles have been published on (1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadec-2-ene-4,11-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242116573D          

 41 44  0  0  0  0            999 V2000
   -2.8838    1.5837    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    0.3260   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7735   -0.8351    0.5046 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9023   -2.0054    0.7572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4824   -1.6838    1.1650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0994   -0.7561    0.1528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1197   -1.4687   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -0.3736    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.2627    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -0.9732    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.8184    1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1287    0.3533    0.9301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4158    1.0158   -0.1375 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9363    1.0037    0.1534 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2146    1.6145   -1.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4820    2.9850   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2742    1.4484   -0.9302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8773    0.8374   -2.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105    0.2909   -1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0405   -0.1563   -2.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.5052    0.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2105    2.3336    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7137    1.3444    0.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3833    2.0837   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6672   -1.1925   -0.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898   -0.4902    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9326   -2.7595   -0.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426   -2.5746    1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -2.6666    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -1.3246    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369   -0.9349   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310   -2.4049   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8464   -1.8154   -1.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0215   -2.2816    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7726    2.0417   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.4114   -1.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634    1.6643    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    1.2408   -1.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    3.3351   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088    2.4050   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6090    0.9544    1.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  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  6  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 17 21  1  0  0  0  0
 19  2  1  0  0  0  0
 21  2  1  0  0  0  0
 21  6  1  0  0  0  0
 14  8  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  0  0  0  0
  5 30  1  0  0  0  0
  7 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  9 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 14 37  1  1  0  0  0
 15 38  1  6  0  0  0
 16 39  1  0  0  0  0
 17 40  1  1  0  0  0
 21 41  1  1  0  0  0
M  END

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
   -2.8838    1.5837    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    0.3260   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7735   -0.8351    0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9023   -2.0054    0.7572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4824   -1.6838    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0994   -0.7561    0.1528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1197   -1.4687   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -0.3736    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.2627    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -0.9732    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.8184    1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1287    0.3533    0.9301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4158    1.0158   -0.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9363    1.0037    0.1534 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2146    1.6145   -1.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4820    2.9850   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2742    1.4484   -0.9302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8773    0.8374   -2.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105    0.2909   -1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0405   -0.1563   -2.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.5052    0.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2105    2.3336    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7137    1.3444    0.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3833    2.0837   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6672   -1.1925   -0.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898   -0.4902    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9326   -2.7595   -0.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426   -2.5746    1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -2.6666    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -1.3246    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369   -0.9349   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310   -2.4049   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8464   -1.8154   -1.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0215   -2.2816    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7726    2.0417   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.4114   -1.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634    1.6643    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    1.2408   -1.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    3.3351   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088    2.4050   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6090    0.9544    1.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 17 21  1  0
 19  2  1  0
 21  2  1  0
 21  6  1  0
 14  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  9 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  1
 15 38  1  6
 16 39  1  0
 17 40  1  1
 21 41  1  1
M  END


  Mrv1652306242116573D          

 41 44  0  0  0  0            999 V2000
   -2.8838    1.5837    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    0.3260   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7735   -0.8351    0.5046 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9023   -2.0054    0.7572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4824   -1.6838    1.1650 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0994   -0.7561    0.1528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1197   -1.4687   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -0.3736    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.2627    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -0.9732    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.8184    1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1287    0.3533    0.9301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4158    1.0158   -0.1375 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9363    1.0037    0.1534 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2146    1.6145   -1.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4820    2.9850   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2742    1.4484   -0.9302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8773    0.8374   -2.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105    0.2909   -1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0405   -0.1563   -2.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.5052    0.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2105    2.3336    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7137    1.3444    0.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3833    2.0837   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6672   -1.1925   -0.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898   -0.4902    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9326   -2.7595   -0.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426   -2.5746    1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -2.6666    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -1.3246    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369   -0.9349   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310   -2.4049   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8464   -1.8154   -1.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0215   -2.2816    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7726    2.0417   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.4114   -1.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634    1.6643    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    1.2408   -1.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    3.3351   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088    2.4050   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6090    0.9544    1.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  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  6  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 17 21  1  0  0  0  0
 19  2  1  0  0  0  0
 21  2  1  0  0  0  0
 21  6  1  0  0  0  0
 14  8  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  0  0  0  0
  5 30  1  0  0  0  0
  7 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  9 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 14 37  1  1  0  0  0
 15 38  1  6  0  0  0
 16 39  1  0  0  0  0
 17 40  1  1  0  0  0
 21 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0011629

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])[C@@]2([H])OC(=O)[C@@]3(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@@](C4=C([H])C(=O)OC([H])([H])[C@@]14[H])(C([H])([H])[H])[C@@]23[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O5/c1-15-4-3-5-16(2)13(15)12(21-14(16)19)11(18)8-7-20-10(17)6-9(8)15/h6,8,11-13,18H,3-5,7H2,1-2H3/t8-,11+,12-,13-,15-,16+/m1/s1

> <INCHI_KEY>
AHMYWLVSCSDIAQ-WDQVFQSZSA-N

> <FORMULA>
C16H20O5

> <MOLECULAR_WEIGHT>
292.331

> <EXACT_MASS>
292.131073744

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
29.682963643304777

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-2-ene-4,11-dione

> <ALOGPS_LOGP>
1.00

> <JCHEM_LOGP>
1.2596373219999997

> <ALOGPS_LOGS>
-2.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.201233006159725

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.545814328541084

> <JCHEM_PKA_STRONGEST_BASIC>
-3.333901845353326

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
73.2318

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.19e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-2-ene-4,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
   -2.8838    1.5837    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    0.3260   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7735   -0.8351    0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9023   -2.0054    0.7572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4824   -1.6838    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0994   -0.7561    0.1528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1197   -1.4687   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -0.3736    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.2627    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -0.9732    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.8184    1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1287    0.3533    0.9301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4158    1.0158   -0.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9363    1.0037    0.1534 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2146    1.6145   -1.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4820    2.9850   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2742    1.4484   -0.9302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8773    0.8374   -2.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105    0.2909   -1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0405   -0.1563   -2.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.5052    0.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2105    2.3336    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7137    1.3444    0.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3833    2.0837   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6672   -1.1925   -0.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898   -0.4902    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9326   -2.7595   -0.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426   -2.5746    1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -2.6666    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -1.3246    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369   -0.9349   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310   -2.4049   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8464   -1.8154   -1.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0215   -2.2816    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7726    2.0417   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.4114   -1.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634    1.6643    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    1.2408   -1.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    3.3351   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088    2.4050   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6090    0.9544    1.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 17 21  1  0
 19  2  1  0
 21  2  1  0
 21  6  1  0
 14  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  9 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  1
 15 38  1  6
 16 39  1  0
 17 40  1  1
 21 41  1  1
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      -2.884   1.584   0.266  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.145   0.326  -0.149  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.773  -0.835   0.505  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.902  -2.005   0.757  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.482  -1.684   1.165  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.099  -0.756   0.153  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.120  -1.469  -1.171  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.524  -0.374   0.432  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.336  -1.263   0.912  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.730  -0.973   1.208  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.532  -1.818   1.674  0.00  0.00           O+0
HETATM   12  O   UNK     0       4.129   0.353   0.930  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.416   1.016  -0.138  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.936   1.004   0.153  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.215   1.615  -1.027  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.482   2.985  -0.997  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.274   1.448  -0.930  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.877   0.837  -2.047  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.111   0.291  -1.630  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.041  -0.156  -2.338  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.683   0.505   0.178  0.00  0.00           C+0
HETATM   22  H   UNK     0      -2.211   2.334   0.726  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.714   1.344   0.994  0.00  0.00           H+0
HETATM   24  H   UNK     0      -3.383   2.084  -0.589  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.667  -1.192  -0.057  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.190  -0.490   1.497  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.933  -2.760  -0.083  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.343  -2.575   1.629  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.060  -2.667   1.089  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.465  -1.325   2.196  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.637  -0.935  -1.971  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.731  -2.405  -0.997  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.846  -1.815  -1.528  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.022  -2.282   1.120  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.773   2.042  -0.239  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.558   0.411  -1.070  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.763   1.664   1.042  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.650   1.241  -1.976  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.631   3.335  -0.099  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.809   2.405  -0.755  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.609   0.954   1.167  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   19   21                                             
CONECT    3    2    4   25   26                                             
CONECT    4    3    5   27   28                                             
CONECT    5    4    6   29   30                                             
CONECT    6    5    7    8   21                                             
CONECT    7    6   31   32   33                                             
CONECT    8    6    9   14                                                  
CONECT    9    8   10   34                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   35   36                                             
CONECT   14   13   15    8   37                                             
CONECT   15   14   16   17   38                                             
CONECT   16   15   39                                                       
CONECT   17   15   18   21   40                                             
CONECT   18   17   19                                                       
CONECT   19   18   20    2                                                  
CONECT   20   19                                                            
CONECT   21   17    2    6   41                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
CONECT   27    4                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    5                                                            
CONECT   31    7                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    9                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   17                                                            
CONECT   41   21                                                            
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
   -2.8838    1.5837    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    0.3260   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7735   -0.8351    0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9023   -2.0054    0.7572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4824   -1.6838    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0994   -0.7561    0.1528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1197   -1.4687   -1.1713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241   -0.3736    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3358   -1.2627    0.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -0.9732    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.8184    1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1287    0.3533    0.9301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4158    1.0158   -0.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9363    1.0037    0.1534 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2146    1.6145   -1.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4820    2.9850   -0.9972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2742    1.4484   -0.9302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8773    0.8374   -2.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105    0.2909   -1.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0405   -0.1563   -2.3385 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.5052    0.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2105    2.3336    0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7137    1.3444    0.9936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3833    2.0837   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6672   -1.1925   -0.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898   -0.4902    1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9326   -2.7595   -0.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3426   -2.5746    1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -2.6666    1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -1.3246    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6369   -0.9349   -1.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7310   -2.4049   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8464   -1.8154   -1.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0215   -2.2816    1.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7726    2.0417   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    0.4114   -1.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7634    1.6643    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    1.2408   -1.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    3.3351   -0.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8088    2.4050   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6090    0.9544    1.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 17 21  1  0
 19  2  1  0
 21  2  1  0
 21  6  1  0
 14  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  9 34  1  0
 13 35  1  0
 13 36  1  0
 14 37  1  1
 15 38  1  6
 16 39  1  0
 17 40  1  1
 21 41  1  1
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₆H₂₀O₅

Average Mass

292.3310 Da

Monoisotopic Mass

292.13107 Da

IUPAC Name

(1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-2-ene-4,11-dione

Traditional Name

(1S,7S,8S,9S,12S,16R)-8-hydroxy-1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadec-2-ene-4,11-dione

CAS Registry Number

Not Available

SMILES

C[C@]12CCC[C@@]3(C)[C@H]1[C@H](OC2=O)[C@@H](O)[C@@H]1COC(=O)C=C31

InChI Identifier

InChI=1S/C16H20O5/c1-15-4-3-5-16(2)13(15)12(21-14(16)19)11(18)8-7-20-10(17)6-9(8)15/h6,8,11-13,18H,3-5,7H2,1-2H3/t8-,11+,12-,13-,15-,16+/m1/s1

InChI Key

AHMYWLVSCSDIAQ-WDQVFQSZSA-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
Aspergillus	NPAtlas	23521163

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Dihydropyranone
Pyran
Gamma butyrolactone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	ALOGPS
logP	1.26	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	13.55	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	73.23 m³·mol⁻¹	ChemAxon
Polarizability	29.68 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

NPA019241

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30771217

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146684753

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Deng C, Huang C, Wu Q, Pang J, Lin Y: A new sesquiterpene from the mangrove endophytic fungus Aspergillus terreus (No. GX7-3B). Nat Prod Res. 2013 Oct;27(20):1882-7. doi: 10.1080/14786419.2013.778847. Epub 2013 Mar 22. [PubMed:23521163 ]

Showing NP-Card for Botryosphaerin F (NP0011629)

MOL for NP0011629 (Botryosphaerin F)

3D MOL for NP0011629 (Botryosphaerin F)

3D SDF for NP0011629 (Botryosphaerin F)

3D-SDF for NP0011629 (Botryosphaerin F)

PDB for NP0011629 (Botryosphaerin F)

3D PDB for NP0011629 (Botryosphaerin F)

SMILES for NP0011629 (Botryosphaerin F)

INCHI for NP0011629 (Botryosphaerin F)

Structure for NP0011629 (Botryosphaerin F)

3D Structure for NP0011629 (Botryosphaerin F)