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Uridine Monophosphate

PubChem CID: 6030

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Compound Synonyms Uridine 5'-monophosphate, 58-97-9, 5'-URIDYLIC ACID, Uridylic acid, Uridine monophosphate, uridine-5'-monophosphate, Uridine phosphate, Uridine 5'-phosphate, Uridine 5'-phosphoric acid, 5'-UMP, UMP, UMP (nucleic acid), uridylate, Uridine 5'-(dihydrogen phosphate), 5'Uridylic acid, Uridylicacid, CHEBI:16695, BRN 0047486, UNII-E2OU15WN0N, EINECS 200-408-0, E2OU15WN0N, MFCD00067346, [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate, CHEMBL214393, 5-24-06-00173 (Beilstein Handbook Reference), U 5'-P, {[(2R,3S,4R,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid, Uridylic Acids, 2,4(1H,3H)-pyrimidinedione, 1-(5-O-phosphono-beta-D-ribofuranosyl)-, Acids, Uridylic, Acid, Uridylic, ((2R,3S,4R,5R)-5-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate, U5P, 5'-uridylic acid (8CI)(9CI), C9H13N2O9P, Monophosphate, Uridine, 27416-86-0, 5'-Monophosphate, Uridine, uridine-phosphate, URIDINE 5' MONOPHOSPHATE, 1loq, 5'-ridylic acid, uridine-monophosphate, UridylsA currencyure, 5'-Uridylic acid,, uridine-5'-phosphate, Uridylic acid (6CI), 1xz8, Uridine 5'-phosphorate, 5'-Uridylic acid, UMP, bmse000280, Epitope ID:196258, SCHEMBL157644, GTPL5125, 5'-URIDYLIC ACID [MI], DTXSID20883211, MSK6906, Uridine mono(dihydrogen phosphate), URIDINE PHOSPHATE [WHO-DD], Uridine-5'-(dihydrogen phosphate), BDBM50398699, s9451, Uridine 5'-monophosphate (Standard), AKOS016009839, 1ST6906, DB03685, HY-101981R, NU05691, NCGC00163325-01, AC-32138, AS-56739, BP-58611, HY-101981, CS-0022391, Uridine, mono(dihydrogen phosphate) (ester), UMP, Uridylic acid, D-Uridine 5'-monophosphate, C00105, F20483, Uridine 5 inverted exclamation marka-monophosphate, Q27074278, 954D2AA9-0360-4F63-A7BF-63254220F1F3, [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl dihydrogen phosphate, 200-408-0
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 166.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CCC(C2CCCC2)C(C)C1
Np Classifier Class Pyrimidine nucleos(t)ides
Deep Smiles O[C@@H][C@H]O)[C@H]O[C@H]5nccc=O)[nH]c6=O)))))))))COP=O)O)O
Heavy Atom Count 21.0
Classyfire Class Pyrimidine nucleotides
Description Uridine monophosphate, also known as uridylic acid or ump, is a member of the class of compounds known as pyrimidine ribonucleoside monophosphates. Pyrimidine ribonucleoside monophosphates are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety. Uridine monophosphate is soluble (in water) and a moderately acidic compound (based on its pKa). Uridine monophosphate can be found in a number of food items such as dill, towel gourd, pineappple sage, and arrowroot, which makes uridine monophosphate a potential biomarker for the consumption of these food products. Uridine monophosphate can be found primarily in blood and saliva. Uridine monophosphate exists in all living species, ranging from bacteria to humans. In humans, uridine monophosphate is involved in several metabolic pathways, some of which include pyrimidine metabolism, tetracycline action pathway, spectinomycin action pathway, and arbekacin action pathway. Uridine monophosphate is also involved in several metabolic disorders, some of which include dihydropyrimidinase deficiency, beta ureidopropionase deficiency, UMP synthase deficiency (orotic aciduria), and congenital disorder of glycosylation cdg-iid.
Scaffold Graph Node Level OC1CCN(C2CCCO2)C(O)N1
Classyfire Subclass Pyrimidine ribonucleotides
Isotope Atom Count 0.0
Molecular Complexity 517.0
Database Name cmaup_ingredients;fooddb_chem_all;hmdb_chem_all;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 4.0
Uniprot Id P21589, P30085, Q96P26, Q9BXI3, Q8TCD5, Q9NPB1, P49961, Q8WVQ1, O75355, Q9HA47, P22413, O14638, P15291, Q9BY32, P50583, Q9Y227, O75354, O75356, P11172, Q9H3H5, O95848, Q9BZX2, Q9H0P0, Q8NE73, P49902, Q5EBM0, Q9NWZ5, Q5MY95, Q96AZ6, Q3T906, Q96BW1, P49798, Q8T6J6, O26232, Q9NUW8, Q9UKV8, Q96SW2
Iupac Name [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
Prediction Hob 0.0
Class Pyrimidine nucleotides
Veber Rule False
Classyfire Superclass Nucleosides, nucleotides, and analogues
Target Id NPT1394
Xlogp -3.6
Superclass Nucleosides, nucleotides, and analogues
Subclass Pyrimidine ribonucleotides
Gsk 4 400 Rule True
Molecular Formula C9H13N2O9P
Scaffold Graph Node Bond Level O=c1ccn(C2CCCO2)c(=O)[nH]1
Prediction Swissadme 0.0
Inchi Key DJJCXFVJDGTHFX-XVFCMESISA-N
Silicos It Class Soluble
Fcsp3 0.5555555555555556
Logs -0.313
Rotatable Bond Count 4.0
State Solid
Logd -1.569
Synonyms 5'-UMP, 5'Uridylic acid, pU, UMP, Uridine 5'-(dihydrogen phosphate), Uridine 5'-phosphate, Uridine 5'-phosphoric acid, Uridine monophosphate, URIDINE-5'-monophosphATE, Uridylate, Uridylic acid, 5'Uridylate, Uridine 5'-(dihydrogen phosphoric acid), Uridine monophosphoric acid, URIDINE-5'-monophosphoric acid, Uridine 5'-monophosphoric acid, Uridine 5'-phosphorate, Uridine mono(dihydrogen phosphate), Uridine phosphate, Acids, uridylic, monoPhosphate, uridine, 5'-monoPhosphate, uridine, Uridylic acids, Acid, uridylic, Uridine 5' monophosphate, uridine monophosphate
Esol Class Highly soluble
Functional Groups CO, COC, COP(=O)(O)O, c=O, c[nH]c, cn(c)C
Compound Name Uridine Monophosphate
Kingdom Organic compounds
Prediction Hob Swissadme 0.0
Exact Mass 324.036
Formal Charge 0.0
Monoisotopic Mass 324.036
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 324.18
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 4.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aromatic heteromonocyclic compounds
Lipinski Rule Of 5 True
Esol -0.2727569714285717
Inchi InChI=1S/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
Smiles C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
Nring 2.0
Np Classifier Biosynthetic Pathway Carbohydrates
Defined Bond Stereocenter Count 0.0
Egan Rule False
Taxonomy Direct Parent Pyrimidine ribonucleoside monophosphates
Np Classifier Superclass Nucleosides

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