NP-MRD: Showing NP-Card for (-)-Cochliospicin A (NP0083042)

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Record Information

Version

2.0

Created at

2022-04-29 04:05:29 UTC

Updated at

2022-04-29 04:05:29 UTC

NP-MRD ID

NP0083042

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Cochliospicin A

Description

(3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-1,3,4,5,7,8-hexahydrospiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. (-)-Cochliospicin A is found in Cochliobolus spicifer. Based on a literature review very few articles have been published on (3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-1,3,4,5,7,8-hexahydrospiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -3.1937   -2.1393   -0.9668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8611   -0.7425   -0.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4713   -0.7810    0.1164 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4676   -1.7799    1.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4911   -1.2301   -0.9174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8425   -1.7657   -2.0021 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9087   -1.0308   -0.6375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3138   -0.3518    0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311    0.3799    1.2175 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    0.8077    2.3257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147    0.5512    0.6265 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9779    1.2391    1.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5632    2.3558    0.6607 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1915    3.6107    1.1193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9556    2.1665   -0.6740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3963    2.6359   -1.7410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8438    1.3964   -0.5186 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7539   -0.4060    0.7100 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1780    0.3922    1.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5031   -0.0839   -0.5420 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7491    1.3937   -0.7270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9148   -0.5600   -1.6779 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0075   -1.5679   -1.5154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -2.8695   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2336   -2.4312   -0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1882   -2.1465   -2.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9008   -0.0345   -1.3218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5834   -0.4326    0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4843   -1.9355    1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8395   -1.4135    2.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0188   -2.7323    0.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7658    0.6139    1.9430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4016    1.7080    2.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6594    2.2503    0.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3623    4.2444    0.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9873   -1.4859    0.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7897   -0.0872    2.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8914    1.4397    1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    0.3471    1.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5111   -0.5855   -0.4545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9080    1.9437    0.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421    1.5728   -1.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8152    1.8114   -1.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5325   -1.7736   -2.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4414   -2.4934   -1.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  6
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 11  3  1  0
 11 17  1  6
 23  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  4 31  1  0
 18 36  1  1
 19 37  1  0
 19 38  1  0
 19 39  1  0
 20 40  1  1
 21 41  1  0
 21 42  1  0
 21 43  1  0
 23 44  1  0
 23 45  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  6
 14 35  1  0
M  END


  Mrv1652304292206052D          

 23 25  0  0  1  0            999 V2000
    2.0564   -2.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6988   -1.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9194   -0.3798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9000   -1.3812    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6795   -2.1762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2576   -2.7647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0370   -3.5596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3770   -2.9437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465   -2.8932    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6529   -2.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4205   -1.7920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0429   -1.6513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9713   -3.5298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6658   -0.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1133   -1.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0652   -0.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0757   -1.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6539   -2.1453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4333   -2.9403    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6345   -3.1468    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4140   -3.9417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0115   -3.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  1  0  0  0
 10 14  1  1  0  0  0
  5 15  1  6  0  0  0
  5 16  1  1  0  0  0
 16 17  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  1  0  0  0
 20 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0083042

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@]1(C)C(=O)C2=C([C@H](C)[C@H](C)OC2)C(=O)[C@]11C[C@@H](O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O6/c1-5-16(4)13(19)10-7-22-9(3)8(2)12(10)14(20)17(16)6-11(18)15(21)23-17/h8-9,11,18H,5-7H2,1-4H3/t8-,9+,11-,16+,17-/m1/s1

> <INCHI_KEY>
YXBCBQJJLPBBMD-XGSISSNYSA-N

> <FORMULA>
C17H22O6

> <MOLECULAR_WEIGHT>
322.357

> <EXACT_MASS>
322.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
32.80691299949094

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-1,3,4,5,7,8-hexahydrospiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

> <ALOGPS_LOGP>
1.19

> <JCHEM_LOGP>
1.7566536326666662

> <ALOGPS_LOGS>
-1.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.586687466701822

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8543829020646223

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
80.83250000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-3,4-dihydro-1H-spiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.839  -4.775   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.250  -3.291   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.171  -2.193   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.583  -0.709   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.680  -2.578   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.268  -4.062   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.348  -5.161   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.936  -6.645   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.704  -5.495   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.833  -5.401   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.219  -3.910   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.652  -3.345   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       0.080  -3.082   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -1.813  -6.589   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.243  -1.102   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.211  -2.115   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.122  -0.611   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.741  -2.906   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.821  -4.005   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.409  -5.489   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.918  -5.874   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.506  -7.358   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.488  -6.587   0.000  0.00  0.00           C+0
CONECT    1    2    7   21                                                  
CONECT    2    1    3   18                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   15   16                                             
CONECT    6    5    7    9   13                                             
CONECT    7    6    1    8                                                  
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6                                                       
CONECT   14   10                                                            
CONECT   15    5                                                            
CONECT   16    5   17                                                       
CONECT   17   16                                                            
CONECT   18    2   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20    1   22                                                  
CONECT   22   21                                                            
CONECT   23   20                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₂O₆

Average Mass

322.3570 Da

Monoisotopic Mass

322.14164 Da

IUPAC Name

(3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-1,3,4,5,7,8-hexahydrospiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

Traditional Name

(3S,4S,4'R,6S,7R)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-3,4-dihydro-1H-spiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

CAS Registry Number

Not Available

SMILES

CC[C@@]1(C)C(=O)C2=C([C@H](C)[C@H](C)OC2)C(=O)[C@]11C[C@@H](O)C(=O)O1

InChI Identifier

InChI=1S/C17H22O6/c1-5-16(4)13(19)10-7-22-9(3)8(2)12(10)14(20)17(16)6-11(18)15(21)23-17/h8-9,11,18H,5-7H2,1-4H3/t8-,9+,11-,16+,17-/m1/s1

InChI Key

YXBCBQJJLPBBMD-XGSISSNYSA-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
Cochliobolus spicifer	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

Not Available

Direct Parent

Benzopyrans

Alternative Parents

Substituents

Benzopyran
Cyclohexenone
Alpha-acyloxy ketone
Pyran
Gamma butyrolactone
Tetrahydrofuran
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
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	1.19	ALOGPS
logP	1.76	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	12.59	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	80.83 m³·mol⁻¹	ChemAxon
Polarizability	32.81 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

163034987

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Cochliospicin A (NP0083042)

MOL for NP0083042 ((-)-Cochliospicin A)

3D MOL for NP0083042 ((-)-Cochliospicin A)

3D SDF for NP0083042 ((-)-Cochliospicin A)

3D-SDF for NP0083042 ((-)-Cochliospicin A)

PDB for NP0083042 ((-)-Cochliospicin A)

3D PDB for NP0083042 ((-)-Cochliospicin A)

SMILES for NP0083042 ((-)-Cochliospicin A)

INCHI for NP0083042 ((-)-Cochliospicin A)

Structure for NP0083042 ((-)-Cochliospicin A)

3D Structure for NP0083042 ((-)-Cochliospicin A)