NP-MRD: Showing NP-Card for (1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol (NP0249676)

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Record Information

Version

2.0

Created at

2022-09-07 12:17:45 UTC

Updated at

2022-09-07 12:17:45 UTC

NP-MRD ID

NP0249676

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol

Description

(1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-4H-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]Pentadecan]-14'-ene-9,15'-diol belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. (1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol is found in Penicillium roqueforti. Based on a literature review very few articles have been published on (1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-4H-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]Pentadecan]-14'-ene-9,15'-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072214172D          

 34 40  0  0  1  0            999 V2000
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M  END

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M  END


  Mrv1652309072214172D          

 34 40  0  0  1  0            999 V2000
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 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 18 33  1  0  0  0  0
  8 34  1  0  0  0  0
  2 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0249676

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@H]2C[C@]34CCCCN3C[C@@]2(C[C@@]11C(O)=NC2=C1C=CC1=C2OC=CC(C)(C)O1)N=C4O

> <INCHI_IDENTIFIER>
InChI=1S/C27H33N3O4/c1-23(2)10-12-33-20-17(34-23)8-7-16-19(20)28-22(32)27(16)14-25-15-30-11-6-5-9-26(30,21(31)29-25)13-18(25)24(27,3)4/h7-8,10,12,18H,5-6,9,11,13-15H2,1-4H3,(H,28,32)(H,29,31)/t18-,25-,26+,27-/m1/s1

> <INCHI_KEY>
SGIZPBSMKAKPSO-KVPGOQOISA-N

> <FORMULA>
C27H33N3O4

> <MOLECULAR_WEIGHT>
463.578

> <EXACT_MASS>
463.247106555

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
51.16311957463405

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-4H-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-9,15'-diol

> <JCHEM_LOGP>
1.7608930506086766

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.268008294035762

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.1078803941313105

> <JCHEM_PKA_STRONGEST_BASIC>
6.992421745447283

> <JCHEM_POLAR_SURFACE_AREA>
86.88000000000001

> <JCHEM_REFRACTIVITY>
129.93559999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-9,15'-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      19.005   4.209   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.934   2.670   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.449   2.943   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.536   1.253   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.804  -0.102   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      17.289  -0.374   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      16.131   0.641   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.202   2.179   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.906   3.011   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.538   2.304   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.466   0.765   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.763  -0.066   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      14.373  -1.556   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      12.835  -1.645   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.004  -2.942   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      12.275  -0.211   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.973  -1.076   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.536  -0.370   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.944  -1.031   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       6.757   0.227   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       5.186  -0.150   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.969   0.849   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.307   2.382   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.833   2.805   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.155   1.902   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.767   2.561   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.962   1.296   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.550   1.185   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.696   2.718   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.898   1.929   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.552   1.442   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.916   2.157   0.000  0.00  0.00           O+0
HETATM   33  N   UNK     0       8.154   0.093   0.000  0.00  0.00           N+0
HETATM   34  O   UNK     0      17.450   3.082   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   34                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   34                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   11   17   28                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   27   33                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20   26   31                                             
CONECT   26   25   27                                                       
CONECT   27   26   18   28                                                  
CONECT   28   27   16   29   30                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   25   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   18                                                       
CONECT   34    8    2                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₃N₃O₄

Average Mass

463.5780 Da

Monoisotopic Mass

463.24711 Da

IUPAC Name

(1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-4H-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-9,15'-diol

Traditional Name

(1'S,8R,8'S,10'R)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-9,15'-diol

CAS Registry Number

Not Available

SMILES

CC1(C)[C@H]2C[C@]34CCCCN3C[C@@]2(C[C@@]11C(O)=NC2=C1C=CC1=C2OC=CC(C)(C)O1)N=C4O

InChI Identifier

InChI=1S/C27H33N3O4/c1-23(2)10-12-33-20-17(34-23)8-7-16-19(20)28-22(32)27(16)14-25-15-30-11-6-5-9-26(30,21(31)29-25)13-18(25)24(27,3)4/h7-8,10,12,18H,5-6,9,11,13-15H2,1-4H3,(H,28,32)(H,29,31)/t18-,25-,26+,27-/m1/s1

InChI Key

SGIZPBSMKAKPSO-KVPGOQOISA-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 roqueforti	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Azaspirodecane
Quinolizidine
3-alkylindole
Indole or derivatives
1,4-dioxepine
Alkyl aryl ether
Dioxepine
Aralkylamine
Tetrahydropyridine
Piperidine
Benzenoid
Cyclic carboximidic acid
Tertiary aliphatic amine
Tertiary amine
Organic 1,3-dipolar compound
Azacycle
Oxacycle
Ether
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Amine
Organic oxygen 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	1.76	ChemAxon
pKa (Strongest Acidic)	2.11	ChemAxon
pKa (Strongest Basic)	6.99	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	86.88 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	129.94 m³·mol⁻¹	ChemAxon
Polarizability	51.16 Å³	ChemAxon
Number of Rings	7	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

139585636

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol (NP0249676)

MOL for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

3D MOL for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

3D SDF for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

3D-SDF for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

PDB for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

3D PDB for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

SMILES for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

INCHI for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

Structure for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)

3D Structure for NP0249676 ((1's,8r,8's,10'r)-4,4,11',11'-tetramethyl-3',14'-diazaspiro[[1,4]dioxepino[2,3-g]indole-8,12'-tetracyclo[6.5.2.0¹,¹⁰.0³,⁸]pentadecan]-14'-ene-9,15'-diol)