NP-MRD: Showing NP-Card for Comp7 (NP0350924)

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Record Information

Version

2.0

Created at

2025-04-08 16:02:46 UTC

Updated at

2025-07-24 18:36:04 UTC

NP-MRD ID

NP0350924

Natural Product DOI

https://doi.org/10.57994/3909

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Comp7

Description

Comp7 was first documented in 2021 (PMID: 32410501). Based on a literature review a small amount of articles have been published on Comp7 (PMID: 37513188).

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01192318282D          

 18 20  0  0  1  0            999 V2000
    3.3122    0.9048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2882    0.0801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0899   -0.1147    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3219   -0.9064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1466   -0.9304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242   -0.1535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7711    0.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7186   -0.5167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0898   -1.0507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3876   -0.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5825    0.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4051    0.2464    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8382    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4466    1.6748    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6299    1.1807    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9507   -1.3084    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7523   -1.5032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -2.2949    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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  3  7  1  0  0  0  0
  8  2  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0350924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(=N)N1CCC[C@@]11NC(=O)[C@@H]2CCCN2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C11H17N5O2/c12-10(13)16-6-2-4-11(16)9(18)15-5-1-3-7(15)8(17)14-11/h7H,1-6H2,(H3,12,13)(H,14,17)/t7-,11+/m0/s1

> <INCHI_KEY>
LCVSEJNMGHICMW-WRWORJQWSA-N

> <FORMULA>
C11H17N5O2

> <MOLECULAR_WEIGHT>
251.29

> <EXACT_MASS>
251.138224807

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
25.193184488420037

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,8'aS)-1',4'-dioxo-hexahydro-1'H-spiro[pyrrolidine-2,3'-pyrrolo[1,2-a]pyrazine]-1-carboximidamide

> <JCHEM_LOGP>
-1.682423056162271

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.529283583453713

> <JCHEM_PKA_STRONGEST_BASIC>
10.854698323964069

> <JCHEM_POLAR_SURFACE_AREA>
102.52000000000001

> <JCHEM_REFRACTIVITY>
74.39589999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,8'aS)-1',4'-dioxo-tetrahydro-2'H-spiro[pyrrolidine-2,3'-pyrrolo[1,2-a]pyrazine]-1-carboximidamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JAN-23         0                                  
HETATM    1  O   UNK     0       6.183   1.689   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.138   0.150   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       7.634  -0.214   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       8.068  -1.692   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.607  -1.737   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.125  -0.287   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.906   0.654   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.075  -0.964   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.901  -1.961   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.590  -1.153   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.954   0.344   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.490   0.460   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       5.298   1.771   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       4.567   3.126   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       6.776   2.204   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0       5.508  -2.442   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       7.004  -2.806   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.438  -4.284   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    3                                                       
CONECT    8    2    9   12   16                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    8   17                                                       
CONECT   17   16    4   18                                                  
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₇N₅O₂

Average Mass

251.2900 Da

Monoisotopic Mass

251.13822 Da

IUPAC Name

(2R,8'aS)-1',4'-dioxo-hexahydro-1'H-spiro[pyrrolidine-2,3'-pyrrolo[1,2-a]pyrazine]-1-carboximidamide

Traditional Name

(2R,8'aS)-1',4'-dioxo-tetrahydro-2'H-spiro[pyrrolidine-2,3'-pyrrolo[1,2-a]pyrazine]-1-carboximidamide

CAS Registry Number

Not Available

SMILES

NC(=N)N1CCC[C@@]11NC(=O)[C@@H]2CCCN2C1=O

InChI Identifier

InChI=1S/C11H17N5O2/c12-10(13)16-6-2-4-11(16)9(18)15-5-1-3-7(15)8(17)14-11/h7H,1-6H2,(H3,12,13)(H,14,17)/t7-,11+/m0/s1

InChI Key

LCVSEJNMGHICMW-WRWORJQWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D2O, experimental)	niwakanji0218@gmail.com	University of California, Los Angeles	Kanji Niwa	2025-04-08	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

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	-1.7	ChemAxon
pKa (Strongest Acidic)	10.53	ChemAxon
pKa (Strongest Basic)	10.85	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	102.52 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	74.4 m³·mol⁻¹	ChemAxon
Polarizability	25.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yin Z, Liu S, Yang X, Chen M, Du J, Liu H, Yang L: LSD1-Based Reversible Inhibitors Virtual Screening and Binding Mechanism Computational Study. Molecules. 2023 Jul 10;28(14):5315. doi: 10.3390/molecules28145315. [PubMed:37513188 ]
Bhattacharjee P, Sarkar S, Shmatova OI, Nenajdenko VG, Pandya P, Bhadra K: Synthetic carboline compounds targeting protein: biophysical and biological perspective. J Biomol Struct Dyn. 2021 Jul;39(10):3703-3720. doi: 10.1080/07391102.2020.1769732. Epub 2020 Jun 1. [PubMed:32410501 ]

Showing NP-Card for Comp7 (NP0350924)

MOL for NP0350924 (Comp7)

3D MOL for NP0350924 (Comp7)

3D SDF for NP0350924 (Comp7)

3D-SDF for NP0350924 (Comp7)

PDB for NP0350924 (Comp7)

3D PDB for NP0350924 (Comp7)

SMILES for NP0350924 (Comp7)

INCHI for NP0350924 (Comp7)

Structure for NP0350924 (Comp7)

3D Structure for NP0350924 (Comp7)