SCHEMBL1835932

SCHEMBL1835932

O=c1ccn([C@H]2C[C@H](F)[C@@H](CO)O2)c(=O)[nH]1

nearest known ligand 0.55

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SLC28A1 O00337 1/20 0.55
SLC28A2 O43868 1/20 0.55
SLC29A1 Q99808 1/20 0.55
SLC28A3 Q9HAS3 1/20 0.55
DUT P33316 4/20 0.51
LMNA P02545 2/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
ALOX12 P18054 1/20 0.46
ADRA1A P35348 1/20 0.46
TK1 P04183 2/20 0.45
TK2 O00142 1/20 0.42
P2RY2 P41231 1/20 0.41
P2RY6 Q15077 1/20 0.41

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
SCHEMBL21423137 1.00 SLC28A1 (0.55) SLC28A1SLC28A2SLC29A1SLC28A3DUT
SCHEMBL19657189 1.00 SLC28A1 (0.55) SLC28A1SLC28A2SLC29A1SLC28A3DUT
SCHEMBL2056679 1.00 SLC28A1 (0.55) SLC28A1SLC28A2SLC29A1SLC28A3DUT
SCHEMBL1835930 1.00 SLC28A1 (0.55) SLC28A1SLC28A2SLC29A1SLC28A3DUT
SCHEMBL1835935 1.00 SLC28A1 (0.55) SLC28A1SLC28A2SLC29A1SLC28A3DUT
SCHEMBL9083132 0.87 LMNA (0.46) SLC28A1SLC28A2SLC29A1SLC28A3LMNA
Deoxyuridine SCHEMBL24512520 0.85 DUT (0.64) SLC28A1SLC28A2SLC29A1SLC28A3DUT
Deoxyuridine SCHEMBL19841232 0.85 DUT (0.64) SLC28A1SLC28A2SLC29A1SLC28A3DUT
Deoxyuridine SCHEMBL391224 0.85 DUT (0.64) SLC28A1SLC28A2SLC29A1SLC28A3DUT
Deoxyuridine SCHEMBL9708874 0.85 DUT (0.64) SLC28A1SLC28A2SLC29A1SLC28A3DUT

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 161 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20150150893-A1 ANDROGRAPHOLIDE ANALOGS AND THEIR USE FOR MEDICATION LIAONING LIFENG SCIENT & TECHNOLOGY DEV COMPANY LTD (CN) 2015-06-04 US claimed
EP-2509949-B1 PYRIDINONE HYDROXYCYCLOPENTYL CARBOXAMIDES: HIV INTEGRASE INHIBITORS WITH THERAPEUTIC APPLICATIONS UNIV GEORGIA (US) 2014-04-23 EP claimed
US-8703801-B2 Pyridinone hydroxycyclopentyl carboxamides: HIV integrase inhibitors with therapeutic applications UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2014-04-22 US claimed
US-20120282218-A1 PYRIDINONE HYDROXYCYCLOPENTYL CARBOXAMIDES: HIV INTEGRASE INHIBITORS WITH THERAPEUTIC APPLICATIONS UNIVERSITY OF GEORGIA RESEARCH FOUNDATION INC. (US) 2012-11-08 US claimed
EP-2509949-A2 PYRIDINONE HYDROXYCYCLOPENTYL CARBOXAMIDES: HIV INTEGRASE INHIBITORS WITH THERAPEUTIC APPLICATIONS University Of Georgia Research Foundation, Inc. (US) 2012-10-17 EP claimed
WO-2011071849-A2 PYRIDINONE HYDROXYCYCLOPENTYL CARBOXAMIDES: HIV INTEGRASE INHIBITORS WITH THERAPEUTIC APPLICATIONS UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2011-06-16 WO claimed
US-20100092427-A1 Pyridinone Diketo Acids: Inhibitors of HIV Replication in Combination Therapy THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION (US) 2010-04-15 US claimed
EP-2046328-A2 PYRIDINONE DIKETO ACIDS: INHIBITORS OF HIV REPLICATION IN COMBINATION THERAPY UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2009-04-15 EP claimed
WO-2008010953-A2 PYRIDINONE DIKETO ACIDS: INHIBITORS OF HIV REPLICATION IN COMBINATION THERAPY UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2008-01-24 WO claimed
US-20070264241-A1 Compounds for Enhanced Cancer Therapy ZGENE A/S (DK) 2007-11-15 US claimed
WO-1994026762-A1 PREPARATION OF FLUORO-NUCLEOSIDES AND INTERMEDIATES FOR USE THEREIN RHONE-POULENC CHEMICALS LIMITED (GB) 1994-11-24 WO claimed
WO-1994005686-A1 ANOMERISATION PROCESS UNIVERSITY OF BIRMINGHAM (GB) 1994-03-17 WO claimed
EP-0577725-A1 TARGETED DRUG DELIVERY VIA MIXED PHOSPHATE DERIVATIVES UNIVERSITY OF FLORIDA (US) 1994-01-12 EP claimed
US-5177064-A TARGETED DRUG DELIVERY VIA PHOSPHONATE DERIVATIVES UNIVERSITY OF FLORIDA (US) 1993-01-05 US claimed
US-5159067-A 5'-Diphosphohexose nucleoside pharmaceutical compositions UNIVERSITY OF GEORGIA RESEARCH FOUNDATION INC. (US) 1992-10-27 US claimed
WO-1992017185-A1 TARGETED DRUG DELIVERY VIA MIXED PHOSPHATE DERIVATIVES UNIVERSITY OF FLORIDA (US) 1992-10-15 WO claimed
WO-1991000867-A1 5'-DIPHOSPHOHEXOSE NUCLEOSIDE PHARMACEUTICAL COMPOSITIONS UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 1991-01-24 WO claimed
EP-0254268-B1 FLUORINATED NUCLEOSIDES,THEIR PREPARATION AND THEIR PHARMACEUTICAL USE AGAINST AIDS THE WELLCOME FOUNDATION LIMITED (GB) 1990-09-19 EP claimed
EP-0316592-A2 3'-Fluoro-2',3'-dideoxyuridine, and its therapeutic application Stichting REGA V.Z.W. (BE) 1989-05-24 EP claimed
EP-0317128-A2 Anti-HIV Pyrimidine Nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1989-05-24 EP claimed

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

For each of this compound's patents that has machine-readable text (4 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-20100092427-A1 Pyridinone Diketo Acids: Inhibitors of HIV Replication in Combination Therapy TKT, DHFR, DTYMK SLC28A1 1466/4885SLC28A2 1696/4885SLC29A1 530/4885
US-20120282218-A1 PYRIDINONE HYDROXYCYCLOPENTYL CARBOXAMIDES: HIV INTEGRASE INHIBITORS WITH THERAPEUTIC APPLICATIONS PAICS, DUT, AADAC SLC28A1 615/4885SLC28A2 582/4885SLC29A1 179/4885
US-20150150893-A1 ANDROGRAPHOLIDE ANALOGS AND THEIR USE FOR MEDICATION CYP11B1, CYP51A1, CYP11B2 SLC28A1 1555/4885SLC28A2 2118/4885SLC29A1 2242/4885
US-20070264241-A1 Compounds for Enhanced Cancer Therapy TYMP, BAD, NUDT1 SLC28A1 217/4885SLC28A2 204/4885SLC29A1 52/4885

“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.