NP-MRD: Showing NP-Card for Millmerranone E (NP0333224)

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Record Information

Version

2.0

Created at

2024-05-12 21:45:27 UTC

Updated at

2026-02-17 17:11:14 UTC

NP-MRD ID

NP0333224

Natural Product DOI

https://doi.org/10.57994/2555

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Millmerranone E

Description

Millmerranone E was first documented in 2021 (PMID: 34636579).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652311162200012D          

 37 42  0  0  1  0            999 V2000
    2.5883   -5.1687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1650   -4.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5666   -3.7400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9899   -4.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1433   -3.0319    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5449   -2.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3698   -2.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7931   -3.0068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1947   -2.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3915   -3.7274    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4902   -4.5465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148   -4.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6397   -4.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0413   -3.7023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8662   -3.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2895   -4.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1144   -4.3853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5160   -3.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3409   -3.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7642   -4.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5891   -4.3477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0125   -5.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3626   -5.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5377   -5.0935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8879   -5.1186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630   -5.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6614   -5.8518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6180   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7199   -2.3237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -3.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492   -2.2298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5389   -2.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9168   -3.7651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401   -4.4732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7974   -5.0946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0388   -4.7705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1125   -3.9488    0.0000 O   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  1  6  0  0  0
  3  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  6  0  0  0
  8 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
  8 28  1  0  0  0  0
  5 29  1  1  0  0  0
  5 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  2  0  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 37  1  0  0  0  0
M  END


  Mrv1652311162200012D          

 37 42  0  0  1  0            999 V2000
    2.5883   -5.1687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1650   -4.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5666   -3.7400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9899   -4.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1433   -3.0319    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5449   -2.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3698   -2.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7931   -3.0068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1947   -2.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3915   -3.7274    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4902   -4.5465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148   -4.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6397   -4.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0413   -3.7023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8662   -3.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2895   -4.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1144   -4.3853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5160   -3.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3409   -3.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7642   -4.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5891   -4.3477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0125   -5.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3626   -5.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5377   -5.0935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8879   -5.1186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630   -5.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6614   -5.8518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6180   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7199   -2.3237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -3.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492   -2.2298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5389   -2.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9168   -3.7651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401   -4.4732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7974   -5.0946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0388   -4.7705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1125   -3.9488    0.0000 O   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  1  6  0  0  0
  3  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  6  0  0  0
  8 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
  8 28  1  0  0  0  0
  5 29  1  1  0  0  0
  5 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  2  0  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0333224

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=CC2=C(C[C@@]3(O)[C@@](C)(CC[C@@]4(O)C(C)(C)C5=C(OCO5)C(=O)[C@]34C)O2)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C28H30O9/c1-24(2)22-20(34-14-35-22)21(29)26(4)27(24,31)11-10-25(3)28(26,32)13-17-19(37-25)12-18(36-23(17)30)15-6-8-16(33-5)9-7-15/h6-9,12,31-32H,10-11,13-14H2,1-5H3/t25-,26+,27-,28-/m1/s1

> <INCHI_KEY>
WILZSAQYQFRKJW-JUDWXZBOSA-N

> <FORMULA>
C28H30O9

> <MOLECULAR_WEIGHT>
510.539

> <EXACT_MASS>
510.188982546

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
53.61612706718498

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,10R,13R)-1,10-dihydroxy-17-(4-methoxyphenyl)-2,9,9,13-tetramethyl-5,7,14,18-tetraoxapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{15,20}]henicosa-4(8),15(20),16-triene-3,19-dione

> <JCHEM_LOGP>
1.795143952666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.793839715829996

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.870906015826137

> <JCHEM_PKA_STRONGEST_BASIC>
-3.406206969443204

> <JCHEM_POLAR_SURFACE_AREA>
120.75000000000003

> <JCHEM_REFRACTIVITY>
133.6193

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,10R,13R)-1,10-dihydroxy-17-(4-methoxyphenyl)-2,9,9,13-tetramethyl-5,7,14,18-tetraoxapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{15,20}]henicosa-4(8),15(20),16-triene-3,19-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-NOV-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-NOV-22         0                                  
HETATM    1  O   UNK     0       4.832  -9.648   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.041  -8.327   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.791  -6.981   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.581  -8.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -5.659   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.750  -4.314   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.290  -4.291   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.080  -5.613   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.830  -4.267   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.331  -6.958   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.515  -8.487   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.121  -8.280   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.661  -8.256   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.410  -6.911   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.950  -6.888   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.740  -8.209   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.280  -8.186   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.030  -6.841   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.570  -6.817   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.360  -8.139   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      17.900  -8.116   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      18.690  -9.438   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.610  -9.484   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.070  -9.508   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.991  -9.555   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.451  -9.578   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.701 -10.923   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.620  -5.589   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       3.211  -4.338   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.461  -5.683   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.705  -4.162   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.006  -5.178   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.711  -7.028   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.502  -8.350   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.489  -9.510   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.072  -8.905   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.210  -7.371   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4    5   10                                             
CONECT    4    3                                                            
CONECT    5    3    6   29   30                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   28                                             
CONECT    9    8                                                            
CONECT   10    8    3   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15   28                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   17                                                       
CONECT   25   16   26                                                       
CONECT   26   25   13   27                                                  
CONECT   27   26                                                            
CONECT   28   14    8                                                       
CONECT   29    5                                                            
CONECT   30    5   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30   34   37                                                  
CONECT   34   33    2   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   33                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₀O₉

Average Mass

510.5390 Da

Monoisotopic Mass

510.18898 Da

IUPAC Name

(1S,2S,10R,13R)-1,10-dihydroxy-17-(4-methoxyphenyl)-2,9,9,13-tetramethyl-5,7,14,18-tetraoxapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{15,20}]henicosa-4(8),15(20),16-triene-3,19-dione

Traditional Name

(1S,2S,10R,13R)-1,10-dihydroxy-17-(4-methoxyphenyl)-2,9,9,13-tetramethyl-5,7,14,18-tetraoxapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{15,20}]henicosa-4(8),15(20),16-triene-3,19-dione

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=CC2=C(C[C@@]3(O)[C@@](C)(CC[C@@]4(O)C(C)(C)C5=C(OCO5)C(=O)[C@]34C)O2)C(=O)O1

InChI Identifier

InChI=1S/C28H30O9/c1-24(2)22-20(34-14-35-22)21(29)26(4)27(24,31)11-10-25(3)28(26,32)13-17-19(37-25)12-18(36-23(17)30)15-6-8-16(33-5)9-7-15/h6-9,12,31-32H,10-11,13-14H2,1-5H3/t25-,26+,27-,28-/m1/s1

InChI Key

WILZSAQYQFRKJW-JUDWXZBOSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl3, experimental)	taizong.wu@uq.edu.au	Not Available	Not Available	2024-05-12	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600.0, Chloroform-d, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150.0, Chloroform-d, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-17	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Aspergillus sp. CMB-MRF324		Not Available
Aspergillus sp. CMB-MRF324		Not Available

Chemical Taxonomy

Classification

Not classified

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	1.8	ChemAxon
pKa (Strongest Acidic)	12.87	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	120.75 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	133.62 m³·mol⁻¹	ChemAxon
Polarizability	53.62 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

DOI: 10.1021/acs.orglett.1c03150

Showing NP-Card for Millmerranone E (NP0333224)

MOL for NP0333224 (Millmerranone E)

3D MOL for NP0333224 (Millmerranone E)

3D SDF for NP0333224 (Millmerranone E)

3D-SDF for NP0333224 (Millmerranone E)

PDB for NP0333224 (Millmerranone E)

3D PDB for NP0333224 (Millmerranone E)

SMILES for NP0333224 (Millmerranone E)

INCHI for NP0333224 (Millmerranone E)

Structure for NP0333224 (Millmerranone E)

3D Structure for NP0333224 (Millmerranone E)