NP-MRD: Showing NP-Card for (1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione (NP0196386)

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Record Information

Version

2.0

Created at

2022-09-04 14:28:12 UTC

Updated at

2022-09-04 14:28:12 UTC

NP-MRD ID

NP0196386

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione

Description

Fumiquinazoline K belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. (1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione was first documented in 2012 (PMID: 22574452). Based on a literature review very few articles have been published on Fumiquinazoline K.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216282D          

 35 42  0  0  1  0            999 V2000
    8.4177    2.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1052    2.3233    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8726    2.6263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042216282D          

 35 42  0  0  1  0            999 V2000
    8.4177    2.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0196386

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1[C@@H]2CN3[C@H]4N(C(=O)C33CC3)C3=CC=CC=C3[C@]4(O)C[C@@H](N3C(=O)C4=CC=CC=C4N=C23)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H23N5O4/c1-28-19-13-29-23-26(35,15-7-3-5-9-17(15)31(23)24(34)25(29)10-11-25)12-18(22(28)33)30-20(19)27-16-8-4-2-6-14(16)21(30)32/h2-9,18-19,23,35H,10-13H2,1H3/t18-,19-,23+,26-/m1/s1

> <INCHI_KEY>
GKRURBWFDHPOHK-BMQMDXDDSA-N

> <FORMULA>
C26H23N5O4

> <MOLECULAR_WEIGHT>
469.501

> <EXACT_MASS>
469.175004241

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
47.585257686203825

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'R,3'R,15'R,28'S)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1^{3,10}.0^{4,9}.0^{16,25}.0^{18,23}.0^{13,28}]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione

> <JCHEM_LOGP>
0.8169074693333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.374507770229343

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.897564238403216

> <JCHEM_PKA_STRONGEST_BASIC>
2.9477958166348417

> <JCHEM_POLAR_SURFACE_AREA>
96.76

> <JCHEM_REFRACTIVITY>
125.73789999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,3'R,15'R,28'S)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1^{3,10}.0^{4,9}.0^{16,25}.0^{18,23}.0^{13,28}]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      15.713   5.511   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      14.176   5.418   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      13.679   3.900   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      14.876   2.931   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      12.265   3.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.647   3.182   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.530   4.337   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.962   4.902   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.955   3.974   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.238   2.610   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.700   2.549   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.877   3.851   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.594   5.214   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.132   5.276   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       8.062   6.572   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       8.147   8.157   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.919   9.086   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.631   8.664   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.319  10.172   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.781   9.688   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      10.515   7.355   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      12.114   7.722   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.485   6.894   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.275   5.987   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      13.790   6.262   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      14.786   5.087   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.301   5.362   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.297   4.187   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.777   2.738   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.262   2.463   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.266   3.638   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.751   3.363   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      12.231   1.913   0.000  0.00  0.00           O+0
HETATM   34  N   UNK     0      11.755   4.538   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       9.558   6.018   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   35                                             
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   35                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18   20                                                       
CONECT   20   19   18                                                       
CONECT   21   18   22   35                                                  
CONECT   22   21   23                                                       
CONECT   23   22    2   24                                                  
CONECT   24   23   25   34                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26   32                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   24    5                                                  
CONECT   35   21   15    7                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₃N₅O₄

Average Mass

469.5010 Da

Monoisotopic Mass

469.17500 Da

IUPAC Name

(1'R,3'R,15'R,28'S)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1^{3,10}.0^{4,9}.0^{16,25}.0^{18,23}.0^{13,28}]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione

Traditional Name

CAS Registry Number

Not Available

SMILES

CN1[C@@H]2CN3[C@H]4N(C(=O)C33CC3)C3=CC=CC=C3[C@]4(O)C[C@@H](N3C(=O)C4=CC=CC=C4N=C23)C1=O

InChI Identifier

InChI=1S/C26H23N5O4/c1-28-19-13-29-23-26(35,15-7-3-5-9-17(15)31(23)24(34)25(29)10-11-25)12-18(22(28)33)30-20(19)27-16-8-4-2-6-14(16)21(30)32/h2-9,18-19,23,35H,10-13H2,1H3/t18-,19-,23+,26-/m1/s1

InChI Key

GKRURBWFDHPOHK-BMQMDXDDSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Quinazoline
Indole or derivatives
Pyrimidone
Imidazolidinone
Benzenoid
Pyrimidine
Imidazolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Tertiary alcohol
Carboxamide group
Lactam
Carboxylic acid derivative
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Amine
Organooxygen compound
Organonitrogen 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	0.82	ChemAxon
pKa (Strongest Acidic)	12.9	ChemAxon
pKa (Strongest Basic)	2.95	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	96.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	125.74 m³·mol⁻¹	ChemAxon
Polarizability	47.59 Å³	ChemAxon
Number of Rings	8	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

29215534

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71604971

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Afiyatullov SSh, Zhuravleva OI, Antonov AS, Kalinovsky AI, Pivkin MV, Menchinskaya ES, Aminin DL: New metabolites from the marine-derived fungus Aspergillus fumigatus. Nat Prod Commun. 2012 Apr;7(4):497-500. [PubMed:22574452 ]
LOTUS database [Link]

Showing NP-Card for (1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione (NP0196386)

MOL for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

3D MOL for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

3D SDF for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

3D-SDF for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

PDB for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

3D PDB for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

SMILES for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

INCHI for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

Structure for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)

3D Structure for NP0196386 ((1'r,3'r,15'r,28's)-3'-hydroxy-27'-methyl-10',13',17',25',27'-pentaazaspiro[cyclopropane-1,12'-heptacyclo[13.10.2.1³,¹⁰.0⁴,⁹.0¹⁶,²⁵.0¹⁸,²³.0¹³,²⁸]octacosane]-4',6',8',16',18',20',22'-heptaene-11',24',26'-trione)