Uracil

Uracil

SCHEMBL1217600

C#CC.O=c1cc[nH]c(=O)[nH]1

nearest known ligand 0.74

Full drug profile on Sugi Atlas →

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 2/20 0.74
▸ MMP2 P08253 1/20 0.46
▸ TP53 P04637 1/20 0.45
▸ DPYD Q12882 1/20 0.36
▸ TYMP P19971 1/20 0.32
▸ GSK3B P49841 1/20 0.32
▸ BACE1 P56817 1/20 0.32
▸ CA1 P00915 1/20 0.32
▸ ATAD2 Q6PL18 1/20 0.31
▸ FKBP5 Q13451 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Uracil SCHEMBL27874550 0.86 CRBN (0.90) CRBNMMP2TP53DPYDTYMP
Uracil SCHEMBL5089507 0.86 — —
Uracil SCHEMBL8235 0.86 — —
Uracil SCHEMBL3798527 0.86 CRBN (1.00) CRBNMMP2TP53DPYDTYMP
Uracil SCHEMBL11607890 0.86 — —
Uracil SCHEMBL28867999 0.84 CRBN (0.85) CRBNMMP2TP53DPYDTYMP
Uracil SCHEMBL28426792 0.84 CRBN (0.85) CRBNMMP2TP53DPYDTYMP
Uracil SCHEMBL16116311 0.84 — —
Uracil SCHEMBL4664232 0.84 CRBN (0.94) CRBNMMP2TP53DPYDTYMP
Uracil SCHEMBL21385227 0.84 — —

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9512162-B2 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites and oligonucleotides ASED, LLC (US) 2016-12-06 — — US disclosed
US-9493773-B2 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides ASED, LLC (US) 2016-11-15 — — US disclosed
US-9365607-B1 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides ASED, LLC (US) 2016-06-14 — — US disclosed
US-20150252071-A1 Synthesis of Deuterated Ribo Nucleosides, N-Protected Phosphoramidites and Oligonucleotides ASED, LLC 2015-09-10 — — US disclosed
EP-2882769-A2 SYNTHESIS OF DEUTERATED RIBO NUCLEOSIDES, N-PROTECTED PHOSPHORAMIDITES, AND OLIGONUCLEOTIDES Ased, LLC (US) 2015-06-17 — — EP disclosed
EP-2882768-A2 SYNTHESIS OF DEUTERATED RIBO NUCLEOSIDES, N-PROTECTED PHOSPHORAMIDITES, AND OLIGONUCLEOTIDES Ased, LLC (US) 2015-06-17 — — EP disclosed
US-9045521-B2 Synthesis of deuterated ribo nucleosides N-protected phosphoramidites, and oligonucleotides ASED, LLC (US) 2015-06-02 — — US disclosed
US-20150119565-A1 SYNTHESIS OF DEUTERATED RIBO NUCLEOSIDES, N-PROTECTED PHOSPHORAMIDITES, AND OLIGONUCLEOTIDES ASED, LLC 2015-04-30 — — US disclosed
US-8859754-B2 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides ASED, LLC (US) 2014-10-14 — — US disclosed
WO-2014022563-A2 SYNTHESIS OF DEUTERATED RIBO NUCLEOSIDES, N-PROTECTED PHOSPHORAMIDITES, AND OLIGONUCLEOTIDES ASED, LLC (US) 2014-02-06 — — WO disclosed
US-20140039178-A1 Synthesis of deuterated ribo nucleosides N-protected phosphoramidites, and oligonucleotides ASED, LLC 2014-02-06 — — US disclosed
WO-2014022566-A2 SYNTHESIS OF DEUTERATED RIBO NUCLEOSIDES, N-PROTECTED PHOSPHORAMIDITES, AND OLIGONUCLEOTIDES ASED, LLC (US) 2014-02-06 — — WO disclosed
US-20140039175-A1 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides ASED, LLC 2014-02-06 — — US disclosed
US-20110040082-A1 Modifications of antimetabolite gemcitabine for incorporation in CpG oligonucleotides SRIVASTAVA SURESH C 2011-02-17 — — US disclosed
US-7846436-B2 Oligonucleotides and related compounds CHEMGENES CORPORATION (US) 2010-12-07 — — US disclosed
US-20050159375-A1 Novel oligonucleotides and related compounds CHEMGENES CORPORATION 2005-07-21 — — US disclosed
US-6015886-A ANTISENSE AGENTS WITH MODIFICATIONS INCLUDING P-ALKOXY AND 2'-O-METHYL GROUPS; NUCLEASE RESISTANT, ABILITY TO ACTIVATE BACTERIAL RIBONUCLEASE H, FORM STABLE DUPLEXES WITH RNA, AND HAVE STRONG HYDROPHOBICITY FOR EFFICIENT CELLULAR UPTAKE CHEMGENES CORPORATION (US) 2000-01-18 — — US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050159375-A1 Novel oligonucleotides and related compounds DCLRE1B, TYMP, DUT CRBN 2667/4885MMP2 4177/4885TP53 95/4885
US-20140039178-A1 Synthesis of deuterated ribo nucleosides N-protected phosphoramidites, and oligonucleotides NSUN3, RNGTT, DUT CRBN 1964/4885MMP2 4276/4885TP53 1913/4885
US-20110040082-A1 Modifications of antimetabolite gemcitabine for incorporation in CpG oligonucleotides MTAP, TYMP, DUT CRBN 4589/4885MMP2 2844/4885TP53 166/4885
US-20140039175-A1 Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides NSUN3, RNGTT, DUT CRBN 1939/4885MMP2 4355/4885TP53 1755/4885
US-20150252071-A1 Synthesis of Deuterated Ribo Nucleosides, N-Protected Phosphoramidites and Oligonucleotides NSUN3, DUT, RNGTT CRBN 1854/4885MMP2 4277/4885TP53 2043/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

Send feedback