NP-MRD: Showing NP-Card for Rugulovasine B (NP0057966)

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Record Information

Version

2.0

Created at

2022-04-28 03:18:56 UTC

Updated at

2022-04-28 03:18:56 UTC

NP-MRD ID

NP0057966

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Rugulovasine B

Description

ZINC1559985 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. Rugulovasine B is found in Penicillium biforme, Penicillium concavo-rugulosum, Penicillium concavorugulosum, Penicillium purpurogenum, Penicillium islandicum and Talaromyces rugulosus. Based on a literature review very few articles have been published on ZINC1559985.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
   -0.3730    3.6830    0.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0384    2.3842    0.1308 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1061    1.3138    0.1230 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6800    1.1293    1.4135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8130    0.2150    1.0541 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892    0.0291    1.5266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7020   -0.9538    0.8022 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8318   -1.3941   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8308   -2.3412   -1.1311 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7073   -2.5299   -1.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5418   -1.7942   -1.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -0.8439   -0.7342 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6624   -0.6805    0.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6463    0.0125   -0.4222 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5761   -0.6712    0.4802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7466   -0.7374   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9713   -1.3530    0.4516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6575   -0.1026   -1.4234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6413   -0.0140   -2.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629    0.3453   -1.5867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6224    4.1906    1.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7128    3.4841    0.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5737    4.2927   -0.6433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8064    2.2856    0.8308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7088    1.5925   -0.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342    0.7273    2.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1425    2.1044    1.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5122    0.5884    2.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6762   -1.3097    0.9344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7501   -2.9072   -1.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7246   -3.2617   -2.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317   -1.9214   -2.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3441   -1.0541    1.4545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7042   -2.2602    1.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6971   -1.6331   -0.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4639   -0.6148    1.1133 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 20  1  6
 20 18  1  0
 18 19  2  0
 18 16  1  0
 16 17  1  0
 16 15  2  0
 14  3  1  0
 15 14  1  0
 13  5  1  0
 13  8  2  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  3 25  1  6
  4 26  1  0
  4 27  1  0
  6 28  1  0
  7 29  1  0
  9 30  1  0
 10 31  1  0
 11 32  1  0
 17 34  1  0
 17 35  1  0
 17 36  1  0
 15 33  1  0
M  END


  Mrv1652304282205182D          

 20 23  0  0  1  0            999 V2000
    0.5321    1.9368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117    1.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2157    0.6820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9402    1.0767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9606    1.9014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2566    2.3315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6057    0.3504    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4142   -0.4521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6235   -0.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0243   -0.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2019   -0.1864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1149    0.5754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0134   -1.0192    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8041   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0296    1.0581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8337    0.8737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4556    1.4158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9068    0.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1478   -0.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6145   -0.3720    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
  7 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
  7 19  1  0  0  0  0
 18 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057966

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN[C@H]1CC2=CNC3=CC=CC(=C23)[C@]11OC(=O)C(C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H16N2O2/c1-9-7-16(20-15(9)19)11-4-3-5-12-14(11)10(8-18-12)6-13(16)17-2/h3-5,7-8,13,17-18H,6H2,1-2H3/t13-,16-/m0/s1

> <INCHI_KEY>
QTWQJTORJVFWAQ-BBRMVZONSA-N

> <FORMULA>
C16H16N2O2

> <MOLECULAR_WEIGHT>
268.316

> <EXACT_MASS>
268.121177763

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.911483926771233

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,6'S)-4-methyl-6'-(methylamino)-5H-2'-azaspiro[furan-2,7'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),3',8'(12'),9'-tetraen-5-one

> <ALOGPS_LOGP>
2.12

> <JCHEM_LOGP>
2.474189133333333

> <ALOGPS_LOGS>
-3.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.993736705296516

> <JCHEM_PKA_STRONGEST_BASIC>
9.223174878743697

> <JCHEM_POLAR_SURFACE_AREA>
54.12

> <JCHEM_REFRACTIVITY>
76.56760000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,6'S)-4-methyl-6'-(methylamino)-2'-azaspiro[furan-2,7'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),3',8'(12'),9'-tetraen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.993   3.615   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.955   2.076   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.269   1.273   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.622   2.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.660   3.549   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.346   4.352   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.864   0.654   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.507  -0.844   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.031  -1.283   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.912  -0.225   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.377  -0.348   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      -0.214   1.074   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       5.625  -1.902   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       7.101  -1.463   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.655   1.975   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.156   1.631   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.317   2.643   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.293   0.097   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.876  -0.507   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.614  -0.694   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   12                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8   15   19                                             
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11    2                                                       
CONECT   13    8   14                                                       
CONECT   14   13                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18    7                                                       
CONECT   20   18                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆N₂O₂

Average Mass

268.3160 Da

Monoisotopic Mass

268.12118 Da

IUPAC Name

(2S,6'S)-4-methyl-6'-(methylamino)-5H-2'-azaspiro[furan-2,7'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),3',8'(12'),9'-tetraen-5-one

Traditional Name

(2S,6'S)-4-methyl-6'-(methylamino)-2'-azaspiro[furan-2,7'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),3',8'(12'),9'-tetraen-5-one

CAS Registry Number

Not Available

SMILES

CN[C@H]1CC2=CNC3=CC=CC(=C23)[C@]11OC(=O)C(C)=C1

InChI Identifier

InChI=1S/C16H16N2O2/c1-9-7-16(20-15(9)19)11-4-3-5-12-14(11)10(8-18-12)6-13(16)17-2/h3-5,7-8,13,17-18H,6H2,1-2H3/t13-,16-/m0/s1

InChI Key

QTWQJTORJVFWAQ-BBRMVZONSA-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
Penicillium biforme	Fungi	KNApSAcK
Penicillium concavo-rugulosum	Fungi	KNApSAcK
Penicillium concavorugulosum	LOTUS Database	35616633
Penicillium purpurogenum	Fungi	KNApSAcK
Talaromyces islandicus	Fungi	KNApSAcK
Talaromyces rugulosus	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
Aralkylamine
2-furanone
Benzenoid
Dihydrofuran
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Pyrrole
Amino acid or derivatives
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Secondary aliphatic amine
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Secondary amine
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Amine
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	2.12	ALOGPS
logP	2.47	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	15.99	ChemAxon
pKa (Strongest Basic)	9.22	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	54.12 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	76.57 m³·mol⁻¹	ChemAxon
Polarizability	28.91 Å³	ChemAxon
Number of Rings	4	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

8440502

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10265023

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Rugulovasine B (NP0057966)

MOL for NP0057966 (Rugulovasine B)

3D MOL for NP0057966 (Rugulovasine B)

3D SDF for NP0057966 (Rugulovasine B)

3D-SDF for NP0057966 (Rugulovasine B)

PDB for NP0057966 (Rugulovasine B)

3D PDB for NP0057966 (Rugulovasine B)

SMILES for NP0057966 (Rugulovasine B)

INCHI for NP0057966 (Rugulovasine B)

Structure for NP0057966 (Rugulovasine B)

3D Structure for NP0057966 (Rugulovasine B)