NP-MRD: Showing NP-Card for (3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione (NP0306760)

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Record Information

Version

2.0

Created at

2022-09-10 23:26:59 UTC

Updated at

2022-09-10 23:26:59 UTC

NP-MRD ID

NP0306760

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione

Description

Chaetoglobosin A, also known as penochalasin K, belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. (3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione is found in Calonectria kyotensis, Chaetomium subaffine and Penicillium aurantiogriseum. (3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione was first documented in 2021 (PMID: 34575788). Based on a literature review a small amount of articles have been published on Chaetoglobosin A (PMID: 35362678) (PMID: 35949485) (PMID: 35930651) (PMID: 33766309).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112201272D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309112201272D          

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    1.0528   -2.8269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8535   -2.6282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4259   -3.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5395   -1.6250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4257   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -0.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1676   -0.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5970   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0390   -1.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -1.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3401   -0.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -1.2024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    0.0652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8228   -0.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  6  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
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
  9 31  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  2 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0306760

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)C22[C@@H](\C=C/C[C@H](C)\C=C(C)/[C@@H](O)C(=O)\C=C/C2=O)[C@@H]2O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H36N2O5/c1-17-8-7-10-22-29-31(4,39-29)19(3)27-24(15-20-16-33-23-11-6-5-9-21(20)23)34-30(38)32(22,27)26(36)13-12-25(35)28(37)18(2)14-17/h5-7,9-14,16-17,19,22,24,27-29,33,37H,8,15H2,1-4H3,(H,34,38)/b10-7-,13-12-,18-14-/t17-,19-,22-,24-,27-,28+,29-,31+,32?/m0/s1

> <INCHI_KEY>
OUMWCYMRLMEZJH-YOAIXWIWSA-N

> <FORMULA>
C32H36N2O5

> <MOLECULAR_WEIGHT>
528.649

> <EXACT_MASS>
528.262422267

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
56.60002077230681

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3Z,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

> <JCHEM_LOGP>
3.964077324916884

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.826907364981771

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.715631788533537

> <JCHEM_PKA_STRONGEST_BASIC>
5.425207967701368

> <JCHEM_POLAR_SURFACE_AREA>
115.27999999999999

> <JCHEM_REFRACTIVITY>
151.36650000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3Z,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.448   2.087   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.032   1.661   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.800   2.995   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.101   3.820   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.611   5.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.635   3.947   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.053   3.345   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.029   2.154   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.339   0.645   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.834   1.016   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.328   1.387   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.902  -0.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.382  -0.519   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.476  -1.573   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.545  -2.682   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.981  -1.944   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.257  -3.302   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.930  -4.687   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.068  -5.963   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.593  -7.411   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       5.378  -8.358   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       4.102  -7.495   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.608  -7.866   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.539  -6.757   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.965  -5.277   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.460  -4.906   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.528  -6.015   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       4.740  -3.033   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       4.528  -1.508   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.169  -0.783   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.913  -0.835   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.848  -1.947   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.673  -3.247   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.388  -2.437   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.867  -2.192   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.635  -1.269   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.557  -2.244   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.027   0.122   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.536  -0.189   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   38                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   31                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   12                                                       
CONECT   12   11   10   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   31                                                  
CONECT   17   16   18   28                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   22                                                  
CONECT   28   17   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    9   16   32                                             
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36    2   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   88    0
END

View in JSmol

Synonyms

Value	Source
Chaetoglobosin D	MeSH
Penochalasin K	MeSH
Chaetoglobosin F	MeSH
Chaetoglobosin K	MeSH
Chaetoglobosin T	MeSH
Chaetoglobosin V	MeSH
Chaetoglobosin y	MeSH
Chaetoglobosins	MeSH
Chaetoglobosin C	MeSH
Chaetoglobosin Q	MeSH
Chaetoglobosin b	MeSH
Chaetoglobosin e	MeSH
Chaetoglobosin R	MeSH
Chaetoglobosin u	MeSH
Chaetoglobosin W	MeSH

Chemical Formula

C₃₂H₃₆N₂O₅

Average Mass

528.6490 Da

Monoisotopic Mass

528.26242 Da

IUPAC Name

(3Z,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

Traditional Name

(3Z,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)C22[C@@H](\C=C/C[C@H](C)\C=C(C)/[C@@H](O)C(=O)\C=C/C2=O)[C@@H]2O[C@]12C

InChI Identifier

InChI=1S/C32H36N2O5/c1-17-8-7-10-22-29-31(4,39-29)19(3)27-24(15-20-16-33-23-11-6-5-9-21(20)23)34-30(38)32(22,27)26(36)13-12-25(35)28(37)18(2)14-17/h5-7,9-14,16-17,19,22,24,27-29,33,37H,8,15H2,1-4H3,(H,34,38)/b10-7-,13-12-,18-14-/t17-,19-,22-,24-,27-,28+,29-,31+,32?/m0/s1

InChI Key

OUMWCYMRLMEZJH-YOAIXWIWSA-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
Calonectria kyotensis	LOTUS Database	35616633
Chaetomium subaffine	LOTUS Database	35616633
Penicillium aurantiogriseum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Isoindole or derivatives
Oxepane
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrroline
Pyrrole
Cyclic ketone
Secondary alcohol
Ketone
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Oxirane
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	3.96	ChemAxon
pKa (Strongest Acidic)	2.72	ChemAxon
pKa (Strongest Basic)	5.43	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	115.28 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	151.37 m³·mol⁻¹	ChemAxon
Polarizability	56.6 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00000106

Chemspider ID

78443573

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Chaetoglobosin A

METLIN ID

Not Available

PubChem Compound

139586719

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhou J, Chen X, Jin M: [Adulteration identification of wheat flour in chestnut flour based on differences in mycotoxin contamination by liquid chromatography-tandem mass spectrometry]. Se Pu. 2022 Apr;40(4):303-312. doi: 10.3724/SP.J.1123.2021.10021. [PubMed:35362678 ]
Wang Z, Zhao S, Zhang K, Lin C, Ru X, Yang Q: CgVeA, a light signaling responsive regulator, is involved in regulation of chaetoglobosin A biosynthesis and conidia development in Chaetomium globosum. Synth Syst Biotechnol. 2022 Jul 16;7(4):1084-1094. doi: 10.1016/j.synbio.2022.07.002. eCollection 2022 Dec. [PubMed:35949485 ]
Zhao S, Lin C, Cheng M, Zhang K, Wang Z, Zhao T, Yang Q: New insight into the production improvement and resource generation of chaetoglobosin A in Chaetomium globosum. Microb Biotechnol. 2022 Oct;15(10):2562-2577. doi: 10.1111/1751-7915.14111. Epub 2022 Aug 5. [PubMed:35930651 ]
Xiang B, Hao X, Xie Q, Shen G, Liu Y, Zhu X: Deletion of a Rare Fungal PKS CgPKS11 Promotes Chaetoglobosin A Biosynthesis, Yet Defers the Growth and Development of Chaetomium globosum. J Fungi (Basel). 2021 Sep 13;7(9). pii: jof7090750. doi: 10.3390/jof7090750. [PubMed:34575788 ]
Cheng M, Zhao S, Lin C, Song J, Yang Q: Requirement of LaeA for sporulation, pigmentation and secondary metabolism in Chaetomium globosum. Fungal Biol. 2021 Apr;125(4):305-315. doi: 10.1016/j.funbio.2020.11.008. Epub 2020 Dec 3. [PubMed:33766309 ]
LOTUS database [Link]

Showing NP-Card for (3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione (NP0306760)

MOL for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D MOL for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D SDF for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D-SDF for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

PDB for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D PDB for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

SMILES for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

INCHI for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

Structure for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D Structure for NP0306760 ((3z,6r,7z,9s,11z,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)