NP-MRD: Showing NP-Card for 5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one (NP0232833)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 14:12:13 UTC

Updated at

2022-09-06 14:12:14 UTC

NP-MRD ID

NP0232833

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one

Description

5,7,8,12,13-Pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]Tridecan-11-one 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. 5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one is found in Taricha granulosa. 5,7,8,12,13-Pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]Tridecan-11-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.5611   -0.7321    1.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9697   -1.3892    0.6097 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6901   -1.1830    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9067   -2.1258   -0.3103 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4707   -1.8863   -0.3395 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0542   -2.6980   -1.3334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3104   -0.4145   -0.7429 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0605   -0.1160   -1.2387 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5504   -1.1856   -1.9724 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0481    0.2485   -0.1806 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6999   -0.9628    0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1011    0.9415   -0.8256 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4917    1.1955    0.8450 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2419    2.4427    0.1807 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0028    2.7301   -0.3582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1365    3.8477   -0.9157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1571    1.8274   -0.3259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1816    2.3957    0.4437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7992    0.4969    0.3251 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0282   -0.0213    0.8948 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1922    0.7447    1.4257 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3083   -0.3206    2.3055 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3777   -2.9183   -0.7688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0608   -2.0906    0.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4495   -3.5683   -1.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103   -0.2964   -1.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9921    0.7470   -1.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548   -1.1381   -2.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1386   -1.3754    1.2927 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7013   -0.6425    0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8012   -1.7373   -0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0677    0.8198   -1.8002 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2691    1.3581    1.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5414    1.5847   -1.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2623    3.3566    0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4858    0.4685    1.7196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2122    1.6022    2.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6352   -0.0057    3.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10 12  1  6
 10  8  1  0
  8  9  1  0
  8  7  1  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  3 20  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 21 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 13 10  1  0
 19  7  1  0
 17 19  1  0
 11 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
  8 27  1  6
  9 28  1  0
  7 26  1  6
  5 24  1  1
  6 25  1  0
  4 23  1  0
  2  1  1  0
 20 36  1  0
 21 37  1  1
 22 38  1  0
 13 33  1  1
 17 34  1  6
 18 35  1  0
M  END


  Mrv1533004171517122D          

 21 23  0  0  0  0            999 V2000
    1.0342   -0.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291    0.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9820   -0.2462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3781    0.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953   -0.5370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0395    0.9303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7895    0.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1820    0.1785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2193    1.6088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8312    2.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2652    3.0440    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0020    2.3622    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5019    1.6776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1011    1.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845    1.9139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7175    0.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    1.4780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9417    2.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388    2.9341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0853    2.3501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7756    3.1148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0232833

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)C(O)C2C(O)NC(=N)NC22C(O)C1OC(=O)C2O

> <INCHI_IDENTIFIER>
InChI=1S/C11H17N3O7/c1-10(20)3(15)2-7(18)13-9(12)14-11(2)4(16)6(10)21-8(19)5(11)17/h2-7,15-18,20H,1H3,(H3,12,13,14)

> <INCHI_KEY>
PJSIAXHRXKZYIN-UHFFFAOYSA-N

> <FORMULA>
C11H17N3O7

> <MOLECULAR_WEIGHT>
303.271

> <EXACT_MASS>
303.106649899

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
27.065135521015407

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one

> <ALOGPS_LOGP>
-2.09

> <JCHEM_LOGP>
-3.8731646669999997

> <ALOGPS_LOGS>
-0.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.688782560670045

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.770549845166594

> <JCHEM_PKA_STRONGEST_BASIC>
9.27985419638727

> <JCHEM_POLAR_SURFACE_AREA>
175.35999999999996

> <JCHEM_REFRACTIVITY>
73.7353

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.00e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       1.930  -1.326   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.294   0.170   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.700  -0.460   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.706   0.259   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.178  -1.002   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.074   1.737   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.474   1.688   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.206   0.333   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -2.276   3.003   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -1.552   4.372   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -2.362   5.682   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0      -0.004   4.409   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       0.937   3.132   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.055   2.325   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.958   3.573   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.206   1.491   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.192   2.759   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.624   4.248   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.552   5.477   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.026   4.387   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.448   5.814   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   16                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    6   14   20                                             
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    2   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   13   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₇N₃O₇

Average Mass

303.2710 Da

Monoisotopic Mass

303.10665 Da

IUPAC Name

5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one

Traditional Name

5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one

CAS Registry Number

Not Available

SMILES

CC1(O)C(O)C2C(O)NC(=N)NC22C(O)C1OC(=O)C2O

InChI Identifier

InChI=1S/C11H17N3O7/c1-10(20)3(15)2-7(18)13-9(12)14-11(2)4(16)6(10)21-8(19)5(11)17/h2-7,15-18,20H,1H3,(H3,12,13,14)

InChI Key

PJSIAXHRXKZYIN-UHFFFAOYSA-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
Taricha granulosa	LOTUS Database	35616633

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

Quinazoline
Delta valerolactone
Delta_valerolactone
Hydropyrimidine
1,4,5,6-tetrahydropyrimidine
Oxane
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Guanidine
Lactone
Secondary alcohol
Alkanolamine
Carboxylic acid derivative
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Monocarboxylic acid or derivatives
Propargyl-type 1,3-dipolar organic compound
Polyol
Carboximidamide
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-2.1	ALOGPS
logP	-3.9	ChemAxon
logS	-0.7	ALOGPS
pKa (Strongest Acidic)	11.77	ChemAxon
pKa (Strongest Basic)	9.28	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	175.36 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	73.74 m³·mol⁻¹	ChemAxon
Polarizability	27.07 Å³	ChemAxon
Number of Rings	3	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

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

73009211

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one (NP0232833)

MOL for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

3D MOL for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

3D SDF for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

3D-SDF for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

PDB for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

3D PDB for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

SMILES for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

INCHI for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

Structure for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)

3D Structure for NP0232833 (5,7,8,12,13-pentahydroxy-3-imino-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.0¹,⁶]tridecan-11-one)