SCHEMBL2858346

SCHEMBL2858346

CNC(=O)COc1ccccc1

nearest known ligand 0.63

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PKM P14618 1/20 0.63
RECQL P46063 1/20 0.63
KMT2A Q03164 3/20 0.62
ALPL P05186 2/20 0.62
ALPI P09923 2/20 0.62
ALPG P10696 2/20 0.62
MEN1 O00255 1/20 0.62
ALOX15 P16050 1/20 0.61
HPGD P15428 1/20 0.61
HTT P42858 2/20 0.60
GAA P10253 1/20 0.59
NPC1 O15118 3/20 0.56
RAB9A P51151 2/20 0.56
LMNA P02545 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
ALDH1A1 P00352 1/20 0.55
TSHR P16473 1/20 0.55
MAPK10 P53779 1/20 0.55
HSD17B10 Q99714 1/20 0.55

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
Hydrochloric Acid SCHEMBL10955756 0.98 PKM (0.61) PKMRECQLKMT2AALPLALPI
SCHEMBL27536631 0.93 CYP1A2 (0.64) PKMRECQLKMT2AALPLALPI
SCHEMBL17775464 0.86 ALOX15 (0.59) PKMRECQLKMT2AMEN1ALOX15
SCHEMBL4422103 0.86 MEN1 (0.66) PKMRECQLKMT2AMEN1GAA
SCHEMBL10903296 0.83 KMT2A (0.67) KMT2AALPLALPIALPGMEN1
SCHEMBL6539261 0.83 PLA2G4B (0.60) PKMRECQLKMT2AMEN1ALOX15
SCHEMBL20325853 0.83 RAB9A (0.51) PKMRECQLALOX15NPC1RAB9A
SCHEMBL171840 0.82 MEN1 (0.61) PKMRECQLKMT2AMEN1HPGD
SCHEMBL13916156 0.82 KMT2A (0.54) PKMRECQLKMT2AMEN1NPC1
SCHEMBL4427417 0.82 PKM (0.54) PKMRECQLKMT2AMEN1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2661436-B1 NOVEL SULFAMIDE PIPERAZINE DERIVATIVES AS PROTEIN TYROSINE KINASE INHIBITORS AND PHARMACEUTICAL USE THEREOF LEO PHARMA AS (DK) 2016-04-13 EP claimed
WO-2005016883-A2 ACRYLAMIDE DERIVATIVES AS VLA-1 INTEGRIN ANTAGONISTS AND USES THEREOF ICOS CORPORATION (US) 2005-02-24 WO claimed
WO-2022106669-A1 NEW PROCESS FOR THE MANUFACTURE OF TETRAZOLE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2022-05-27 WO disclosed
US-20210252011-A1 TREATMENT OF GLIOBLASTOMA WITH FASN INHIBITORS CORNELL UNIVERSITY 2021-08-19 US disclosed
US-20210214323-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN FORMA THERAPEUTICS, INC. 2021-07-15 US disclosed
US-10995078-B2 Compounds and compositions for inhibition of FASN FORMA THERAPEUTICS, INC. (US) 2021-05-04 US disclosed
EP-3515455-B1 COMPOUNDS FOR TREATMENT OF LIPOPROTEIN METABOLISM DISORDERS UNIV AARHUS (DK) 2021-04-14 EP disclosed
EP-3626705-B1 ISOCYANATE PRODUCTION METHOD ASAHI CHEMICAL IND (JP) 2021-03-24 EP disclosed
EP-3587406-B1 2-HYDROXY-1-{4-[(4-PHENYLPHENYL)CARBONYL]PIPERAZIN-1-YL}ETHAN-1-ONE DERIVATIVES AND RELATED COMPOUNDS AS FATTY ACID SYNTHASE (FASN) INHIBITORS FOR THE TREATMENT OF CANCER FORMA THERAPEUTICS INC (US) 2021-01-27 EP disclosed
US-20200347025-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN FORMA THERAPEUTICS, INC. 2020-11-05 US disclosed
US-10800750-B2 Compounds and compositions for inhibition of FASN FORMA THERAPEUTICS, INC. (US) 2020-10-13 US disclosed
US-4958018-A REACTING A 3-HALOMETHYL-3-CEPHEM WITH A LEAD REDUCING AGENT OTSUKA KAGAKU KABUSHIKI KAISHA (JP) 1990-09-18 US disclosed
US-4524028-A PENICILLINS CIBA-GEIGY CORPORATION (US) 1985-06-18 US disclosed
US-4518533-A Azetidinone-4-disulfides as intermediates for thia-aza compounds with a beta-lactam ring CIBA GEIGY CORPORATION (US) 1985-05-21 US disclosed
US-4515717-A INTERMEDIATES FOR 6-UNSUBSTITUTED PENICILLIN ANTIOBIOTICS CIBA GEIGY CORPORATION (US) 1985-05-07 US disclosed
US-4500457-A TREATING AN ACYLOXYAZETIDINONE WITH MERCAPTO COMPOUND, GLYOYLIC ESTER, HALOGENATION AGENT, AND PHOSPHINE COMPOUNT THEN CYCLIZATION CIBA-GEIGY CORPORATION (US) 1985-02-19 US disclosed
US-4447360-A Intermediates for thia-aza compounds with a β-lactam ring CIBA-GEIGY CORPORATION (US) 1984-05-08 US disclosed
US-4331676-A 2-PENEM COMPOUNDS UNSUBSTITUTED IN THE 6 POSITION CIBA-GEIGY CORPORATION (US) 1982-05-25 US disclosed
US-4234488-A FLUORESCENT DYES BAYER AKTIENGESELLSCHAFT (DE) 1980-11-18 US disclosed
US-4147865-A Benz-(C,D)-indolyl compounds BAYER AKTIENGESELLSCHAFT (DE) 1979-04-03 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-20200347025-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN FASN, FABP1, SCD PKM 2847/4885RECQL 3056/4885KMT2A 4666/4885
US-20210252011-A1 TREATMENT OF GLIOBLASTOMA WITH FASN INHIBITORS AIFM2, FABP7, FASN PKM 4093/4885RECQL 3533/4885KMT2A 3472/4885
US-20210214323-A1 NOVEL COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN FASN, FABP1, SCD PKM 3226/4885RECQL 3360/4885KMT2A 4741/4885
US-10995078-B2 Compounds and compositions for inhibition of FASN FASN, FABP1, SCD PKM 2847/4885RECQL 3056/4885KMT2A 4666/4885
US-10800750-B2 Compounds and compositions for inhibition of FASN FASN, FABP1, SCD PKM 2847/4885RECQL 3056/4885KMT2A 4666/4885

“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.