SCHEMBL2608570

SCHEMBL2608570

CCOC(O)c1cccnc1

nearest known ligand 0.51

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.51
LMNA P02545 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
GAA P10253 1/20 0.46
CFTR P13569 1/20 0.44
SLC6A2 P23975 1/20 0.44
SLC6A4 P31645 1/20 0.44
SLC6A3 Q01959 1/20 0.44
GOPC Q9HD26 1/20 0.44
CYP17A1 P05093 1/20 0.42
TSHR P16473 1/20 0.42
NPC1 O15118 1/20 0.40
KDM4E B2RXH2 1/20 0.40
KCNA5 P22460 2/20 0.40
CYP19A1 P11511 1/20 0.40

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
SCHEMBL6205340 0.81 SLC6A2 (0.47) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL22824153 0.80 CFTR (0.46) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL21064696 0.80 CFTR (0.46) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL20012923 0.80 CFTR (0.46) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL12714386 0.79 SMN1; SMN2 (0.55) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL11068720 0.79 SMN1; SMN2 (0.60) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL29852317 0.77 SMN1; SMN2 (0.50) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL28134029 0.77 SMN1; SMN2 (0.50) SMN1; SMN2LMNAL3MBTL1GAACFTR
SCHEMBL366712 0.77 LMNA (0.52) LMNAL3MBTL1TSHRKDM4E
SCHEMBL23733914 0.76 SMN1; SMN2 (0.52) SMN1; SMN2LMNAL3MBTL1GAACFTR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110869349-A 2- { [2- (phenoxymethyl) pyridin-5-yl ] oxy } ethanamine derivatives and related compounds as pest control agents, e.g. for protecting plants 拜耳作物科学股份公司 2020-03-06 CN disclosed
US-8329926-B2 Antiviral compounds GILEAD SCIENCES, INC. (US) 2012-12-11 US disclosed
US-8324179-B2 Nucleoside analogs for antiviral treatment GILEAD SCIENCES, INC. (US) 2012-12-04 US disclosed
US-8318701-B2 Phosphonate analogs of HIV inhibitor compounds GILEAD SCIENCES, INC. (US) 2012-11-27 US disclosed
US-8163718-B2 Nucleoside analogues containing phosphonate or phosphonamide groups GILEAD SCIENCES, INC. (US) 2012-04-24 US disclosed
US-20110288053-A1 ANTIVIRAL PHOSPHONATE ANALOGS GILEAD SCIENCES, INC. (US) 2011-11-24 US disclosed
US-20110082112-A1 ANTIVIRAL PHOSPHINATE COMPOUNDS GILEAD SCIENCES, INC. (US) 2011-04-07 US disclosed
US-20110081314-A1 ANTIVIRAL PHOSPHINATE COMPOUNDS GILEAD SCIENCES, INC. (US) 2011-04-07 US disclosed
US-20110071101-A1 Nucleoside Phosphonate Analogs BOOJAMRA CONSTANTINE G 2011-03-24 US disclosed
US-7893264-B2 viricides comprising phosphinic acid compounds and/or mixed with carriers, nucleoside analogues, interferons or pegylated interferons; treating hepatitis C or a hepatitis C associated disorders in animals; side effect reduction GILEAD SCIENCES, INC. (US) 2011-02-22 US disclosed
US-7432261-B2 Anti-inflammatory phosphonate compounds GILEAD SCIENCES, INC. (US) 2008-10-07 US disclosed
US-7427636-B2 Inosine monophosphate dehydrogenase inhibitory phosphonate compounds GILEAD SCIENCES, INC. (US) 2008-09-23 US disclosed
US-7427624-B2 Purine nucleoside phosphorylase inhibitory phosphonate compounds GILEAD SCIENCES, INC. (US) 2008-09-23 US disclosed
US-7417055-B2 Kinase inhibitory phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-08-26 US disclosed
US-7407965-B2 Phosphonate analogs for treating metabolic diseases GILEAD SCIENCES, INC. (US) 2008-08-05 US disclosed
US-20080171724-A1 Phosphonate Derivatives of Mycophenolic Acid GILEAD SCIENCES, INC. (US) 2008-07-17 US disclosed
US-20080167270-A1 ANTI-INFECTIVE PHOSPHONATE ANALOGS BOOJAMRA CONSTANTINE G 2008-07-10 US disclosed
US-20080107628-A1 Polymerase inhibitors GILEAD SCIENCES, INC. 2008-05-08 US disclosed
US-20080076738-A1 Phosphonate Analogs Of Hiv Integrase Inhibitor Compounds GILEAD SCIENCES, INC. 2008-03-27 US disclosed
US-20080057031-A1 Antiviral phosphinate compounds GILEAD SCIENCES, INC. (US) 2008-03-06 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 (9 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-20080167270-A1 ANTI-INFECTIVE PHOSPHONATE ANALOGS PHOSPHO1, PGLS, PSPH SMN1; SMN2 4506/4885LMNA 3274/4885L3MBTL1 2791/4885
US-20110071101-A1 Nucleoside Phosphonate Analogs TYMP, PNP, NUDT1 SMN1; SMN2 1122/4885LMNA 1265/4885L3MBTL1 3332/4885
US-20110288053-A1 ANTIVIRAL PHOSPHONATE ANALOGS TYMP, ITPA, PNP SMN1; SMN2 2517/4885LMNA 2918/4885L3MBTL1 2434/4885
US-20080057031-A1 Antiviral phosphinate compounds PHOSPHO1, MAVS, ITPA SMN1; SMN2 1818/4885LMNA 3642/4885L3MBTL1 2134/4885
US-20080107628-A1 Polymerase inhibitors POLR2H, POLR2E, POLR1E SMN1; SMN2 1178/4885LMNA 1186/4885L3MBTL1 4328/4885
US-20110081314-A1 ANTIVIRAL PHOSPHINATE COMPOUNDS PHOSPHO1, MAVS, ITPA SMN1; SMN2 1818/4885LMNA 3642/4885L3MBTL1 2134/4885
US-20080171724-A1 Phosphonate Derivatives of Mycophenolic Acid PPP5C, DUSP15, DUSP4 SMN1; SMN2 4740/4885LMNA 4872/4885L3MBTL1 2040/4885
US-20080076738-A1 Phosphonate Analogs Of Hiv Integrase Inhibitor Compounds TYMP, PNP, PIKFYVE SMN1; SMN2 4116/4885LMNA 2126/4885L3MBTL1 495/4885
US-20110082112-A1 ANTIVIRAL PHOSPHINATE COMPOUNDS HAVCR2, PHOSPHO1, EIF2AK2 SMN1; SMN2 1610/4885LMNA 4056/4885L3MBTL1 2855/4885

“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.