SCHEMBL1479916

SCHEMBL1479916

C[C@H](C(N)=O)c1ccccc1

nearest known ligand 0.77

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 2/20 0.57
ALOX5 P09917 1/20 0.53
PTGS2 P35354 1/20 0.52
POLB P06746 1/20 0.49
TRPM8 Q7Z2W7 1/20 0.47
ADRA2A P08913 1/20 0.46
ADRA2C P18825 1/20 0.46
LMNA P02545 1/20 0.46
HIF1A Q16665 1/20 0.46
KDM4E B2RXH2 1/20 0.46
CYP2D6 P10635 1/20 0.46
SRC P12931 1/20 0.46
FAAH O00519 1/20 0.46

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
SCHEMBL965912 1.00 EPHX1 (0.57) EPHX1ALOX5PTGS2POLBTRPM8
SCHEMBL9705 1.00 EPHX1 (0.57) EPHX1ALOX5PTGS2POLBTRPM8
Hydrochloric Acid SCHEMBL29096650 0.98 EPHX1 (0.55) EPHX1ALOX5PTGS2POLBTRPM8
Water SCHEMBL27340802 0.98 EPHX1 (0.55) EPHX1ALOX5PTGS2POLBTRPM8
Hydrochloric Acid SCHEMBL3308273 0.98 EPHX1 (0.55) EPHX1ALOX5PTGS2POLBTRPM8
Cyclopropane SCHEMBL27764666 0.94 EPHX1 (0.52) EPHX1ALOX5PTGS2POLBTRPM8
SCHEMBL27522920 0.94 PTGS2 (0.62) EPHX1ALOX5PTGS2LMNAHIF1A
Hypophosphorous Acid SCHEMBL31007070 0.92 EPHX1 (0.50) EPHX1ALOX5PTGS2POLBTRPM8
Benzoic Acid SCHEMBL28452765 0.90 TSHR (0.54) EPHX1ALOX5PTGS2POLBTRPM8
Trifluoroacetic Acid SCHEMBL6756447 0.88 EPHX1 (0.51) EPHX1ALOX5PTGS2POLBTRPM8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7985760-B2 Piperidinetriol derivatives as inhibitors of glycosyceramid synthase ACTELION PHARMACEUTICALS LTD. (CH) 2011-07-26 US claimed
US-20110144033-A1 Proteasome Inhibitors and Methods of Using the Same CEPHALON, INC. (US) 2011-06-16 US claimed
US-7915236-B2 Proteasome inhibitors and methods of using the same CEPHALON, INC. (US) 2011-03-29 US claimed
EP-1660507-B9 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON INC (US) 2010-03-24 EP claimed
US-20090291918-A1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2009-11-26 US claimed
EP-1660507-B1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON INC (US) 2009-08-05 EP claimed
EP-1660507-A2 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2006-05-31 EP claimed
US-20060058349-A1 Piperidinetriol derivatives as inhibitors of glycosyceramid synthase OXFORD GLYCOSCIENCES(UK) LTD (GB) 2006-03-16 US claimed
US-20050107307-A1 Proteasome inhibitors and methods of using the same TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-05-19 US claimed
WO-2005021558-A2 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2005-03-10 WO claimed
CN-113735730-B Preparation method of acyl primary amine 广州大学 2023-11-28 CN disclosed
CN-111757940-B Microbiological method for producing amides 哥伦比亚有限公司 2023-11-07 CN disclosed
WO-2023102507-A1 MACROCYCLIC IMMUNOMODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2023-06-08 WO disclosed
EP-3710592-B1 MICROBIOLOGICAL PROCESS FOR THE PREPARATION OF AMIDES COLUMBIA S R L (IT) 2022-08-31 EP disclosed
US-11261468-B2 Microbiological process for the preparation of amides COLUMBIA SRL (IT) 2022-03-01 US disclosed
CN-1419536-A Process for the selective N-formylation of n-hydroxylamines ABBOTT LAB (US) 2003-05-21 CN disclosed
US-20030049807-A1 Micro-organism possessing enantioselective and regioselective nitrile hydratase/amidase activities INSTITUTO BIOCHIMICO ITALIANO GIOVANNI LOREZINI S.P.A. (IT) 2003-03-13 US disclosed
EP-1291435-A2 A micro-organism possessing enantioselective and regioselective nitrile hydratase/amidase activities ISTITUTO BIOCHIMICO ITALIANO GIOVANNI LORENZINI S.p.A. (IT) 2003-03-12 EP disclosed
US-6281003-B1 REACTING RACEMIC AMIDE, CARBOXYLIC ACID OR ESTER WITH HYDROXYLAMINE FRAUNHOFER-GESELLSCHAFT ZUR FORDERUNG DER ANGEWANDTEN FORSCHUNG E. V. (DE) 2001-08-28 US disclosed
US-5258305-A Manufacture of optically active 2-phenylpropionic acid and 2-phenylpropionamide from the nitrile using Rhodococcus equi NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1993-11-02 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 (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-20090291918-A1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME PSMB11, PSMB5, PSMB6 EPHX1 2993/4885ALOX5 2283/4885PTGS2 3653/4885
US-20050107307-A1 Proteasome inhibitors and methods of using the same PSMB11, PSMB5, PSMB6 EPHX1 2993/4885ALOX5 2283/4885PTGS2 3653/4885
US-20060058349-A1 Piperidinetriol derivatives as inhibitors of glycosyceramid synthase CERS2, UGCG, GBA1 EPHX1 1594/4885ALOX5 1843/4885PTGS2 1154/4885
US-20110144033-A1 Proteasome Inhibitors and Methods of Using the Same PSMB11, PSMB5, PSMB6 EPHX1 2993/4885ALOX5 2283/4885PTGS2 3653/4885

“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.