SCHEMBL262290

SCHEMBL262290

C=CCOC(=O)NC(C)(C)C

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
TSHR P16473 3/20 0.39
MAPT P10636 1/20 0.39
CACNA1B Q00975 1/20 0.39
APBA1 Q02410 1/20 0.39
CYP3A4 P08684 1/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
TDP1 Q9NUW8 1/20 0.36
HSD17B10 Q99714 3/20 0.35
KDM4E B2RXH2 2/20 0.35
MAPK1 P28482 1/20 0.35
ADRB2 P07550 1/20 0.35
ADRB1 P08588 1/20 0.35
ADRB3 P13945 1/20 0.35
ALOX15 P16050 1/20 0.34
ALDH1A1 P00352 4/20 0.33
LMNA P02545 1/20 0.33
CASP1 P29466 2/20 0.33
CSNK2A2 P19784 1/20 0.33

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
SCHEMBL28664150 0.83 TSHR (0.37) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL10702387 0.82 KDM4C (0.38) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL10720740 0.82 SMN1; SMN2 (0.37) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL23198789 0.81 ALDH1A1 (0.41) TSHRMAPTCYP3A4SMN1; SMN2ALDH1A1
SCHEMBL14762577 0.81 TSHR (0.35) KMT2ATSHRALOX15LMNAGAA
SCHEMBL29210062 0.79 TSHR (0.34) TSHRALOX15
SCHEMBL10187040 0.77 MEN1 (0.33) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL10187039 0.77 SMN1; SMN2 (0.34) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL10702150 0.77 NAALAD2 (0.39) MEN1KMT2ATSHRMAPTCACNA1B
SCHEMBL22288335 0.76 TSHR (0.33) TSHRALOX15ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116063324-A Inhibitors of BTK and/or RET having macrocyclic structure 赛诺哈勃药业(成都)有限公司 2023-05-05 CN disclosed
EP-2443485-B1 BIOMEDICAL DEVICES BAUSCH & LOMB (US) 2017-11-08 EP disclosed
EP-2443486-B1 BIOMEDICAL DEVICES BAUSCH & LOMB (US) 2017-03-01 EP disclosed
US-9198974-B2 Decorated macromolecular scaffolds MINTAKA FOUNDATION FOR MEDICAL RESEARCH (CH) 2015-12-01 US disclosed
US-20140221569-A1 DECORATED MACROMOLECULAR SCAFFOLDS ORION BIOTECHNOLOGY HOLDING SA (CH) 2014-08-07 US disclosed
US-8293715-B2 10a-Azalide compound crosslinked at 10a- and 12-positions TAISHO PHARMACEUTICAL CO., LTD. (JP) 2012-10-23 US disclosed
US-8293715-B2 10a-Azalide compound crosslinked at 10a- and 12-positions TAISHO PHARMACEUTICAL CO., LTD. (JP) 2012-10-23 US disclosed
EP-2443485-A2 BIOMEDICAL DEVICES Bausch & Lomb Incorporated (US) 2012-04-25 EP disclosed
EP-2443486-A2 BIOMEDICAL DEVICES Bausch & Lomb Incorporated (US) 2012-04-25 EP disclosed
US-8133960-B2 Biomedical devices BAUSCH & LOMB INCORPORATED (US) 2012-03-13 US disclosed
US-7659307-B2 Nonphytotoxic; 4-Bromo-3-methoxy-N-4-[4(trifluoromethyl)phenoxy]phenyl-thiophene-2-carboxamide; 4-[(Allyloxycarbonyl)amino]-3-methoxy-N-4-[4-(trifluoromethyl)phenoxy]phenyl-thiophene-2-carboxamide BAYER CROPSCIENCE S.A. (FR) 2010-02-09 US disclosed
US-7659307-B2 Nonphytotoxic; 4-Bromo-3-methoxy-N-4-[4(trifluoromethyl)phenoxy]phenyl-thiophene-2-carboxamide; 4-[(Allyloxycarbonyl)amino]-3-methoxy-N-4-[4-(trifluoromethyl)phenoxy]phenyl-thiophene-2-carboxamide BAYER CROPSCIENCE S.A. (FR) 2010-02-09 US disclosed
US-20080004287-A1 Substituted Piperidines that Increase P53 Activity and the Uses Thereof SCHERING CORPORATION 2008-01-03 US disclosed
US-20080004287-A1 Substituted Piperidines that Increase P53 Activity and the Uses Thereof SCHERING CORPORATION 2008-01-03 US disclosed
CN-1993362-A Fused Heterocyclic Compounds TAKEDA PHARMACEUTICAL (JP) 2007-07-04 CN disclosed
EP-0579102-B1 Liquid chromatography stationary phases with reduced silanol interactions WATERS INVESTMENTS LTD (US) 1997-09-17 EP disclosed
EP-0476564-B1 Latent carbamate silicon coupling agents and process for preparation and use OSI SPECIALTIES INC (US) 1995-12-27 EP disclosed
US-5374755-A Silica substrate with silanol surface groups blocked by (substituted)dialkylcarbamates MILLIPORE CORPORATION (US) 1994-12-20 US disclosed
EP-0579102-A1 Liquid chromatography stationary phases with reduced silanol interactions WATERS INVESTMENTS LIMITED (US) 1994-01-19 EP disclosed
EP-0476564-A1 Latent carbamate silicon coupling agents and process for preparation and use OSi Specialties, Inc. (US) 1992-03-25 EP 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-20080004287-A1 Substituted Piperidines that Increase P53 Activity and the Uses Thereof TP53, MDM2, TP53BP1 MEN1 3505/4885KMT2A 1308/4885TSHR 4670/4885
US-20140221569-A1 DECORATED MACROMOLECULAR SCAFFOLDS ILK, HAVCR2, MATR3 MEN1 3010/4885KMT2A 4620/4885TSHR 4158/4885

“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.