NP-MRD: Showing NP-Card for 1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one (NP0287994)

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Record Information

Version

2.0

Created at

2022-09-09 17:30:42 UTC

Updated at

2022-09-09 17:30:42 UTC

NP-MRD ID

NP0287994

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one

Description

3',5'-Cyclic dTMP, also known as CTMP or cyclic TMP, belongs to the class of organic compounds known as pyrimidones. Pyrimidones are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. 3',5'-Cyclic dTMP is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one is found in Pisum sativum. 1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one was first documented in 1986 (PMID: 3019316). Based on a literature review very few articles have been published on 3',5'-cyclic dTMP.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -3.3890   -1.5648   -1.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9605   -0.2822   -0.6333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6923   -0.2304   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2362    0.9028    0.5154 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0520    0.9915    1.1238 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5728   -0.2903    1.6757 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6835   -0.5881    0.7014 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7211   -1.3041    1.2334 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9210   -1.3597    0.0365 P   0  0  1  0  0  5  0  0  0  0  0  0
    5.1325   -2.1252    0.4925 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2219   -2.0380   -1.3396 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3061    0.2496   -0.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1262    0.8983   -0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1825    0.8454    0.4674 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0057    1.5139    0.2610 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0289    2.0079    0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6369    3.1022    1.0246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2518    1.9757   -0.0565 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7253    0.8503   -0.6228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9854    0.8043   -1.2052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9048   -1.6641   -2.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1005   -2.4282   -0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5078   -1.6146   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0630   -1.0877   -0.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283    1.7332    1.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0524   -0.1198    2.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1537   -1.0834    1.7953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3357   -0.9595   -0.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4234   -1.5217   -2.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6575    0.4763   -1.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3733    1.9575   -0.8800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7329    1.1777    1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8359    0.7753   -0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 11  1  6
  9 10  2  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
  4 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19  2  1  0
 15  5  1  0
 14  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  5 25  1  1
  6 26  1  0
  6 27  1  0
  7 28  1  6
 11 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  1
 20 33  1  0
M  END


  Mrv1652309092219302D          

 20 22  0  0  1  0            999 V2000
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.6345    0.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1648   -0.4287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -2.1269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  1  0  0  0
  5 15  1  0  0  0  0
  4 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
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287994

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CN([C@H]2C[C@@H]3OP(O)(=O)OC[C@H]3O2)C(=O)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H13N2O7P/c1-5-3-12(10(14)11-9(5)13)8-2-6-7(18-8)4-17-20(15,16)19-6/h3,6-8H,2,4H2,1H3,(H,15,16)(H,11,13,14)/t6-,7+,8+/m0/s1

> <INCHI_KEY>
QSJFDOVQWZVUQG-XLPZGREQSA-N

> <FORMULA>
C10H13N2O7P

> <MOLECULAR_WEIGHT>
304.195

> <EXACT_MASS>
304.046037765

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.23908925197152

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-1-[(6R)-2-hydroxy-2-oxo-hexahydro-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-5-methyl-1,2-dihydropyrimidin-2-one

> <JCHEM_LOGP>
0.021418975000000506

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.4948479472708085

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8574606004720149

> <JCHEM_PKA_STRONGEST_BASIC>
-4.013682717315045

> <JCHEM_POLAR_SURFACE_AREA>
117.89

> <JCHEM_REFRACTIVITY>
62.827600000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-1-[(6R)-2-hydroxy-2-oxo-tetrahydro-4H-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-5-methylpyrimidin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.400   1.365   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -0.320  -1.303   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.924   0.237   0.000  0.00  0.00           O+0
HETATM    9  P   UNK     0       6.258  -0.533   0.000  0.00  0.00           P+0
HETATM   10  O   UNK     0       6.784   0.914   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       7.774  -0.800   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       6.258  -2.073   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.126  -2.549   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.320  -3.970   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      -2.630  -2.637   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      -3.400  -1.303   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.940  -1.303   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6   15                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    7   15                                                  
CONECT   15   14    5                                                       
CONECT   16    4   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    2   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Value	Source
3',5'-Cyclic thymidine monophosphate	ChEBI
CTMP	ChEBI
Cyclic 3',5'-thymidine monophosphate	ChEBI
Cyclic 3',5'-thymidylic acid	ChEBI
Cyclic TMP	ChEBI
Thymidine 3',5'-cyclic monophosphate	ChEBI
Thymidine cyclic 3',5'-phosphate	ChEBI
Thymidine cyclophosphate	ChEBI
Thymidine, cyclic 3',5'-(hydrogen phosphate)	ChEBI
3',5'-Cyclic thymidine monophosphoric acid	Generator
Cyclic 3',5'-thymidine monophosphoric acid	Generator
Cyclic 3',5'-thymidylate	Generator
Thymidine 3',5'-cyclic monophosphoric acid	Generator
Thymidine cyclic 3',5'-phosphoric acid	Generator
Thymidine cyclophosphoric acid	Generator
Thymidine, cyclic 3',5'-(hydrogen phosphoric acid)	Generator

Chemical Formula

C₁₀H₁₃N₂O₇P

Average Mass

304.1950 Da

Monoisotopic Mass

304.04604 Da

IUPAC Name

4-hydroxy-1-[(6R)-2-hydroxy-2-oxo-hexahydro-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-5-methyl-1,2-dihydropyrimidin-2-one

Traditional Name

4-hydroxy-1-[(6R)-2-hydroxy-2-oxo-tetrahydro-4H-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-5-methylpyrimidin-2-one

CAS Registry Number

Not Available

SMILES

CC1=CN([C@H]2C[C@@H]3OP(O)(=O)OC[C@H]3O2)C(=O)N=C1O

InChI Identifier

InChI=1S/C10H13N2O7P/c1-5-3-12(10(14)11-9(5)13)8-2-6-7(18-8)4-17-20(15,16)19-6/h3,6-8H,2,4H2,1H3,(H,15,16)(H,11,13,14)/t6-,7+,8+/m0/s1

InChI Key

QSJFDOVQWZVUQG-XLPZGREQSA-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
Pisum sativum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidones. Pyrimidones are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazines

Sub Class

Pyrimidines and pyrimidine derivatives

Direct Parent

Pyrimidones

Alternative Parents

Substituents

Pyrimidone
Hydropyrimidine
Organic phosphoric acid derivative
Tetrahydrofuran
Heteroaromatic compound
Vinylogous amide
Lactam
Urea
Oxacycle
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

3',5'-cyclic pyrimidine nucleotide (CHEBI:75183 )

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	0.021	ChemAxon
pKa (Strongest Acidic)	1.86	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.89 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	62.83 m³·mol⁻¹	ChemAxon
Polarizability	26.24 Å³	ChemAxon
Number of Rings	3	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

13628274

KEGG Compound ID

Not Available

BioCyc ID

CPD-3733

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12359154

PDB ID

Not Available

ChEBI ID

75183

Good Scents ID

Not Available

References

General References

Newton RP, Kingston EE, Hakeem NA, Salih SG, Beynon JH, Moyse CD: Extraction, purification, identification and metabolism of 3',5'-cyclic UMP, 3',5'-cyclic IMP and 3',5'-cyclic dTMP from rat tissues. Biochem J. 1986 Jun 1;236(2):431-9. doi: 10.1042/bj2360431. [PubMed:3019316 ]
LOTUS database [Link]

Showing NP-Card for 1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one (NP0287994)

MOL for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

3D MOL for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

3D SDF for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

3D-SDF for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

PDB for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

3D PDB for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

SMILES for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

INCHI for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

Structure for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)

3D Structure for NP0287994 (1-[(4ar,6r,7as)-2-hydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-5-methylpyrimidin-2-one)