NP-MRD: Showing NP-Card for 21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol (NP0329181)

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Record Information

Version

2.0

Created at

2022-09-12 13:20:02 UTC

Updated at

2022-09-12 13:20:03 UTC

NP-MRD ID

NP0329181

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol

Description

21-Chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]Tritriaconta-17(31),19(30),20,22(29)-tetraene-5,9-diol 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. 21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol is found in Penicillium crustosum and Penicillium solitum. 21-Chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]Tritriaconta-17(31),19(30),20,22(29)-tetraene-5,9-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251506192D          

 44 53  0  0  0  0            999 V2000
   10.6975    2.7983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4633    2.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0313    1.4089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6611    1.8146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0932    2.4129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2910    2.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7230    2.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9208    2.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6866    1.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1187    2.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8844    1.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7767    2.4601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6502    0.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2182    0.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0204    0.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2546    1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3624    0.4186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0568    1.4292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8225    0.6382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4269    1.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7241    2.9306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2045    2.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5500    1.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053    1.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
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  9 16  1  0  0  0  0
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 23 43  1  0  0  0  0
 43 44  1  0  0  0  0
 32 44  2  0  0  0  0
 40 44  1  0  0  0  0
M  END

     RDKit          3D

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 27 69  1  0
 27 70  1  0
 28 71  1  1
 29 72  1  0
 29 73  1  0
 30 74  1  6
 34 79  1  6
 14 62  1  0
 16 63  1  0
 33 77  1  0
 33 78  1  0
 32 75  1  0
 32 76  1  0
M  END


  Mrv1533004251506192D          

 44 53  0  0  0  0            999 V2000
   10.6975    2.7983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4633    2.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0313    1.4089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6611    1.8146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0932    2.4129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2910    2.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7230    2.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9208    2.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6866    1.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1187    2.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8844    1.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7767    2.4601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6502    0.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2182    0.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0204    0.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2546    1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3624    0.4186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0568    1.4292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8225    0.6382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6247    0.8308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4269    1.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9949    0.4252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8255    0.8295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4704    0.0848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6928   -0.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1601   -0.8705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1570   -0.8181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481    0.1644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1704   -0.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8502    0.8772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6726    0.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0277    1.6867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5603    2.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7379    2.3017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3828    1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5604    1.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506    3.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8733    3.5048    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.3282    3.3091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9556    2.7734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7241    2.9306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2045    2.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5500    1.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053    1.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 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
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 30 35  1  0  0  0  0
 35 36  2  0  0  0  0
 33 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 11 42  1  0  0  0  0
 42 43  2  0  0  0  0
 23 43  1  0  0  0  0
 43 44  1  0  0  0  0
 32 44  2  0  0  0  0
 40 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329181

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C1OC2CCC3(C)C4(C)C(CCC3(O)C22OC2C1O)C1OC(C)(C)C2CC3C2C2=C5C(NC4=C15)=CC(Cl)=C2CC3=C

> <INCHI_IDENTIFIER>
InChI=1S/C37H44ClNO5/c1-15(2)29-28(40)32-37(44-32)23(42-29)9-10-34(6)35(7)19(8-11-36(34,37)41)30-27-26-22(39-31(27)35)14-21(38)18-12-16(3)17-13-20(24(17)25(18)26)33(4,5)43-30/h14,17,19-20,23-24,28-30,32,39-41H,1,3,8-13H2,2,4-7H3

> <INCHI_KEY>
YWORPEZTBDVGCS-UHFFFAOYSA-N

> <FORMULA>
C37H44ClNO5

> <MOLECULAR_WEIGHT>
618.21

> <EXACT_MASS>
617.2908012

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
69.30799208517064

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol

> <ALOGPS_LOGP>
5.57

> <JCHEM_LOGP>
5.360639697666668

> <ALOGPS_LOGS>
-6.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
10

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.412714868698469

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.798320256725923

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6011931834560853

> <JCHEM_POLAR_SURFACE_AREA>
87.24000000000001

> <JCHEM_REFRACTIVITY>
167.5939

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.43e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      19.969   5.224   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      19.532   3.747   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.592   2.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.034   3.387   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      16.974   4.504   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.477   4.144   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.416   5.261   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.919   4.902   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.482   3.425   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.421   4.542   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.984   3.065   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.783   4.592   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.547   1.589   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.607   0.472   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.105   0.832   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.542   2.308   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.743   0.781   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.039   2.668   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      14.602   1.191   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      16.099   1.551   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.597   1.911   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.657   0.794   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.008   1.548   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.345   0.158   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.893  -0.356   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.766  -1.625   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.893  -1.527   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.503   0.307   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.052  -0.207   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.454   1.637   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.989   1.758   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.652   3.149   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.779   4.418   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.244   4.297   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.581   2.907   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.046   2.786   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.761   5.663   0.000  0.00  0.00           C+0
HETATM   38 Cl   UNK     0       3.497   6.542   0.000  0.00  0.00          Cl+0
HETATM   39  C   UNK     0       6.213   6.177   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.384   5.177   0.000  0.00  0.00           C+0
HETATM   41  N   UNK     0       8.818   5.470   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0       9.715   3.938   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.493   3.000   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.103   3.663   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   16                                             
CONECT   10    9                                                            
CONECT   11    9   12   13   42                                             
CONECT   12   11                                                            
CONECT   13   11   14   23                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    9   17   18                                             
CONECT   17   16                                                            
CONECT   18   16    6   19   20                                             
CONECT   19   18   20                                                       
CONECT   20   19   18   21                                                  
CONECT   21   20    4   22                                                  
CONECT   22   21                                                            
CONECT   23   13   24   43                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   28   32                                                  
CONECT   32   31   33   44                                                  
CONECT   33   32   34   37                                                  
CONECT   34   33   35                                                       
CONECT   35   34   30   36                                                  
CONECT   36   35                                                            
CONECT   37   33   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   44                                                  
CONECT   41   40   42                                                       
CONECT   42   41   11   43                                                  
CONECT   43   42   23   44                                                  
CONECT   44   43   32   40                                                  
MASTER        0    0    0    0    0    0    0    0   44    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₄ClNO₅

Average Mass

618.2100 Da

Monoisotopic Mass

617.29080 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=C)C1OC2CCC3(C)C4(C)C(CCC3(O)C22OC2C1O)C1OC(C)(C)C2CC3C2C2=C5C(NC4=C15)=CC(Cl)=C2CC3=C

InChI Identifier

InChI=1S/C37H44ClNO5/c1-15(2)29-28(40)32-37(44-32)23(42-29)9-10-34(6)35(7)19(8-11-36(34,37)41)30-27-26-22(39-31(27)35)14-21(38)18-12-16(3)17-13-20(24(17)25(18)26)33(4,5)43-30/h14,17,19-20,23-24,28-30,32,39-41H,1,3,8-13H2,2,4-7H3

InChI Key

YWORPEZTBDVGCS-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium crustosum	LOTUS Database	35616633
Penicillium solitum	LOTUS Database	35616633

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
Tetralin
3-alkylindole
Indole or derivatives
Indole
1,4-dioxepane
Dioxepane
Pyran
Oxane
Aryl halide
Monosaccharide
Benzenoid
Aryl chloride
Heteroaromatic compound
Cyclic alcohol
Tertiary alcohol
Pyrrole
Secondary alcohol
Dialkyl ether
Oxacycle
Oxirane
Ether
Azacycle
Organic oxygen compound
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	5.57	ALOGPS
logP	5.36	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	12.8	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	87.24 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	167.59 m³·mol⁻¹	ChemAxon
Polarizability	69.31 Å³	ChemAxon
Number of Rings	10	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14411897

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol (NP0329181)

MOL for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

3D MOL for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

3D SDF for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

3D-SDF for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

PDB for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

3D PDB for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

SMILES for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

INCHI for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

Structure for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)

3D Structure for NP0329181 (21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-5,9-diol)