SCHEMBL6579496

SCHEMBL6579496

COc1ccc(C)cc1NC(C)=O

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.66
KMT2A Q03164 8/20 0.63
MEN1 O00255 7/20 0.63
MAPT P10636 6/20 0.63
ALDH1A1 P00352 5/20 0.63
GAA P10253 3/20 0.61
CASP3 P42574 1/20 0.61
SENP7 Q9BQF6 1/20 0.61
SENP6 Q9GZR1 1/20 0.61
TP53 P04637 1/20 0.61
MAPK1 P28482 1/20 0.61
NPC1 O15118 1/20 0.60
RAB9A P51151 1/20 0.60
TSHR P16473 2/20 0.60
L3MBTL1 Q9Y468 2/20 0.58
TDP1 Q9NUW8 1/20 0.58
POLB P06746 1/20 0.58
HSD17B10 Q99714 1/20 0.58
KDM4E B2RXH2 1/20 0.57
STAT3 P40763 1/20 0.57

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
SCHEMBL29451289 1.00 SMN1; SMN2 (0.66) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL28918511 0.98 SMN1; SMN2 (0.64) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL9018859 0.92 KMT2A (0.60) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL11660382 0.87 HPGD (0.70) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL862532 0.87 TSHR (0.70) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL30388763 0.86 EPHX1 (0.72) SMN1; SMN2KMT2AMEN1ALDH1A1NPC1
SCHEMBL3831243 0.86 EPHX1 (0.72) SMN1; SMN2KMT2AMEN1ALDH1A1NPC1
SCHEMBL6543397 0.84 EPHX1 (0.79) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL6464089 0.84 KMT2A (0.61) SMN1; SMN2KMT2AMEN1MAPTALDH1A1
SCHEMBL5534456 0.84 KMT2A (0.66) SMN1; SMN2KMT2AMEN1MAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115368281-B PCVS synthesis process 湖北丽康源化工有限公司 2024-07-02 CN disclosed
CN-115368281-A PCVS (Primary biliary cirrhosis) synthesis process 湖北丽康源化工有限公司 2022-11-22 CN disclosed
CN-113999232-A MAT2A inhibitors 南京正大天晴制药有限公司 2022-02-01 CN disclosed
US-9939454-B2 Fluorogenic pH sensitive dyes and their method of use Life Technologies Corporation (US) 2018-04-10 US disclosed
US-9910051-B2 Fluorogenic pH sensitive dyes and their method of use Life Technologies Corporation (US) 2018-03-06 US disclosed
US-20160287607-A1 NON-RETINOID ANTAGONISTS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND STARGARDT DISEASE THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2016-10-06 US disclosed
US-20160139158-A1 FLUOROGENIC PH SENSITIVE DYES AND THEIR METHOD OF USE Life Technologies Corporation 2016-05-19 US disclosed
US-9333202-B2 Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2016-05-10 US disclosed
US-20150126494-A1 NON-RETINOID ANTAGONISTS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND STARGARDT DISEASE THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2015-05-07 US disclosed
US-20150037834-A1 FLUOROGENIC PH SENSITIVE DYES AND THEIR METHOD OF USE Life Technologies Corporation 2015-02-05 US disclosed
WO-1999026942-A1 5-(2-IMIDAZOLINYLAMINO)-BENZIMIDAZOLE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS .ALPHA.-ADRENOCEPTOR AGONISTS WITH IMPROVED METABOLIC STABILITY THE PROCTER & GAMBLE COMPANY (US) 1999-06-03 WO disclosed
WO-1998034995-A1 COMPOUNDS AND METHODS FOR DOPING LIQUID CRYSTAL HOSTS QUEEN'S UNIVERSITY AT KINGSTON (CA) 1998-08-13 WO disclosed
EP-0445926-B1 Organic materials having sulfonamido linked poly(oxyalkylene) moieties and their preparation MILLIKEN RES CORP (US) 1996-08-21 EP disclosed
US-5240464-A Organic materials having sulfonamido linked poly(oxyalkylene) moieties and their preparation MILLIKEN RESEARCH CORPORATION (US) 1993-08-31 US disclosed
EP-0445926-A2 Organic materials having sulfonamido linked poly(oxyalkylene) moieties and their preparation MILLIKEN RESEARCH CORPORATION (US) 1991-09-11 EP disclosed
US-4600797-A NITRATING AN AMINOBENZENE WHICH HAS A PROTECTEDD AMINO GROUP BAYER AKTIENGESELLSCHAFT (DE) 1986-07-15 US disclosed
EP-0049711-B1 PROCESS FOR THE PRODUCTION OF NITRO-AMINO-BENZENES BAYER AG (DE) 1984-02-29 EP disclosed
EP-0049711-A1 Process for the production of nitro-amino-benzenes BAYER AG (DE) 1982-04-21 EP disclosed
US-4166069-A PROCESS FOR THE PREPARATION OF 2-METHOXY-5-METHYLANILINE-4-SULPHONIC ACID BAYER AKTIENGESELLSCHAFT (DE) 1979-08-28 US disclosed
US-4151203-A Process for the preparation of p-nitroaniline compounds by the alkaline hydrolysis of mixed anilides EASTMAN KODAK COMPANY (US) 1979-04-24 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 (2 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-20150126494-A1 NON-RETINOID ANTAGONISTS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND STARGARDT DISEASE RBP4, RBP1, LRAT SMN1; SMN2 366/4885KMT2A 3434/4885MEN1 4615/4885
US-20160287607-A1 NON-RETINOID ANTAGONISTS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND STARGARDT DISEASE RBP4, RBP1, LRAT SMN1; SMN2 366/4885KMT2A 3434/4885MEN1 4615/4885

“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.