NP-MRD: Showing NP-Card for 1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one (NP0316931)

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Record Information

Version

2.0

Created at

2022-09-11 16:27:28 UTC

Updated at

2022-09-11 16:27:28 UTC

NP-MRD ID

NP0316931

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

3',5'-Cyclic UMP, also known as 3',5'-cump or cyclic UMP, belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups. 3',5'-Cyclic UMP 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,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one is found in Pisum sativum. 1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one was first documented in 2013 (PMID: 23087103). Based on a literature review a small amount of articles have been published on 3',5'-cyclic UMP (PMID: 23342095) (PMID: 24792377) (PMID: 24971548).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 33  0  0  0  0  0  0  0  0999 V2000
    1.2892    1.1004   -1.7718 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1471    0.4875   -1.1102 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4516    0.6533   -1.4735 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4519    0.0499   -0.8407 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7866    0.1922   -1.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1372   -0.7730    0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8120   -0.9215    0.5679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8031   -0.3073   -0.0773 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4372   -0.4936    0.3191 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3515   -1.0280   -0.7108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6355   -0.8250   -0.1822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7262   -1.1923   -1.1174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5833   -0.1331   -1.4315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0528    0.7332   -0.0631 P   0  0  2  0  0  5  0  0  0  0  0  0
   -5.1111    0.0492    0.7333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5531    2.2728   -0.6068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6372    1.0101    0.8597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5720    0.6901    0.0638 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2364    0.8018    0.7311 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3889    0.7635    2.1241 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4626    0.3169   -0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9120   -1.2970    0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5434   -1.5645    1.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4036   -1.2371    1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6680   -1.3190    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3972   -1.6387   -2.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3792   -1.9499   -0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7520    2.8803    0.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6136    1.1579   -0.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2951    1.6939    0.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2744   -0.1729    2.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 14  1  0
 14 16  1  6
 14 15  2  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  4  1  0
  4  5  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  9 19  1  0
  2  8  1  0
 11 18  1  0
 20 31  1  0
 19 30  1  1
 18 29  1  6
 16 28  1  0
 12 26  1  0
 12 27  1  0
 11 25  1  1
  9 24  1  1
  7 23  1  0
  6 22  1  0
  5 21  1  0
M  END


  Mrv1652309112218272D          

 20 22  0  0  1  0            999 V2000
   -0.1712   -2.1269    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
   -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
   -1.4087    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  2  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    4.1648   -0.9672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6345   -1.8857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 O   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 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 18 17  1  1  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0316931

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H]2OP(O)(=O)OC[C@H]2O[C@H]1N1C=CC(O)=NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H11N2O8P/c12-5-1-2-11(9(14)10-5)8-6(13)7-4(18-8)3-17-20(15,16)19-7/h1-2,4,6-8,13H,3H2,(H,15,16)(H,10,12,14)/t4-,6-,7-,8-/m1/s1

> <INCHI_KEY>
NXIHNBWNDCFCGL-XVFCMESISA-N

> <FORMULA>
C9H11N2O8P

> <MOLECULAR_WEIGHT>
306.167

> <EXACT_MASS>
306.02530232

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
24.884377914654635

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxo-hexahydro-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-1,2-dihydropyrimidin-2-one

> <JCHEM_LOGP>
-1.2747695773333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.48570599817071

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8328277307612493

> <JCHEM_PKA_STRONGEST_BASIC>
-3.808820701973006

> <JCHEM_POLAR_SURFACE_AREA>
138.12

> <JCHEM_REFRACTIVITY>
59.9812

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxo-tetrahydro-4H-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  O   UNK     0      -0.320  -3.970   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -2.630  -2.637   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -3.400  -1.303   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.940  -1.303   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -0.320  -1.303   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.126  -0.057   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.258  -0.533   0.000  0.00  0.00           O+0
HETATM   14  P   UNK     0       6.258  -2.073   0.000  0.00  0.00           P+0
HETATM   15  O   UNK     0       7.774  -1.805   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.784  -3.520   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.924  -2.843   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.650  -4.013   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    2    9                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18                                                       
CONECT   18   17   11   19                                                  
CONECT   19   18    9   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'-CUMP	ChEBI
CUMP	ChEBI
Cyclic 3',5'-uridine monophosphate	ChEBI
Cyclic UMP	ChEBI
Uridine, cyclic 3',5'-(hydrogen phosphate)	ChEBI
Cyclic 3',5'-uridine monophosphoric acid	Generator
Uridine, cyclic 3',5'-(hydrogen phosphoric acid)	Generator

Chemical Formula

C₉H₁₁N₂O₈P

Average Mass

306.1670 Da

Monoisotopic Mass

306.02530 Da

IUPAC Name

1-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxo-hexahydro-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxy-1,2-dihydropyrimidin-2-one

Traditional Name

1-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxo-tetrahydro-4H-2lambda5-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H]2OP(O)(=O)OC[C@H]2O[C@H]1N1C=CC(O)=NC1=O

InChI Identifier

InChI=1S/C9H11N2O8P/c12-5-1-2-11(9(14)10-5)8-6(13)7-4(18-8)3-17-20(15,16)19-7/h1-2,4,6-8,13H,3H2,(H,15,16)(H,10,12,14)/t4-,6-,7-,8-/m1/s1

InChI Key

NXIHNBWNDCFCGL-XVFCMESISA-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 pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pentose phosphates

Alternative Parents

Substituents

Pentose phosphate
Glycosyl compound
N-glycosyl compound
Monosaccharide phosphate
Pyrimidone
Hydropyrimidine
Organic phosphoric acid derivative
Pyrimidine
Heteroaromatic compound
Vinylogous amide
Tetrahydrofuran
Lactam
Urea
Secondary alcohol
Azacycle
Oxacycle
Organoheterocyclic compound
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

3',5'-cyclic pyrimidine nucleotide (CHEBI:75175 )

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	-1.3	ChemAxon
pKa (Strongest Acidic)	1.83	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	138.12 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	59.98 m³·mol⁻¹	ChemAxon
Polarizability	24.88 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

2339001

KEGG Compound ID

Not Available

BioCyc ID

CPD-3727

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3081385

PDB ID

Not Available

ChEBI ID

75175

Good Scents ID

Not Available

References

General References

Beste KY, Seifert R: cCMP, cUMP, cTMP, cIMP and cXMP as possible second messengers: development of a hypothesis based on studies with soluble guanylyl cyclase alpha(1)beta(1). Biol Chem. 2013 Feb;394(2):261-70. doi: 10.1515/hsz-2012-0282. [PubMed:23087103 ]
Reinecke D, Schwede F, Genieser HG, Seifert R: Analysis of substrate specificity and kinetics of cyclic nucleotide phosphodiesterases with N'-methylanthraniloyl-substituted purine and pyrimidine 3',5'-cyclic nucleotides by fluorescence spectrometry. PLoS One. 2013;8(1):e54158. doi: 10.1371/journal.pone.0054158. Epub 2013 Jan 14. [PubMed:23342095 ]
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LOTUS database [Link]

Showing NP-Card for 1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one (NP0316931)

MOL for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

3D MOL for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

3D SDF for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

3D-SDF for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

PDB for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

3D PDB for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

SMILES for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

INCHI for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

Structure for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)

3D Structure for NP0316931 (1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one)