SCHEMBL3884597

SCHEMBL3884597

CCOC(=O)c1cnoc1C

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.50
ALDH1A1 P00352 3/20 0.47
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47
HSD17B10 Q99714 1/20 0.43
LMNA P02545 2/20 0.43
RAB9A P51151 1/20 0.43
GAA P10253 1/20 0.42
MAPK1 P28482 1/20 0.42
CA12 O43570 2/20 0.42
CA1 P00915 2/20 0.42
CA2 P00918 2/20 0.42
CA7 P43166 2/20 0.42
CA9 Q16790 2/20 0.42
CA14 Q9ULX7 2/20 0.42
HSP90AA1 P07900 1/20 0.42
CYP1A2 P05177 1/20 0.42
KDM4E B2RXH2 2/20 0.41
MAPT P10636 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41

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
SCHEMBL30597835 0.85 TSHR (0.54) TSHRALDH1A1HSD17B10LMNARAB9A
SCHEMBL26987310 0.84 TSHR (0.48) TSHRALDH1A1MEN1KMT2AHSD17B10
SCHEMBL30597839 0.82 TSHR (0.56) TSHRALDH1A1HSD17B10LMNARAB9A
SCHEMBL15856620 0.82 TSHR (0.47) TSHRALDH1A1MEN1KMT2AHSD17B10
SCHEMBL13815776 0.81 RAB9A (0.55) TSHRALDH1A1HSD17B10LMNARAB9A
SCHEMBL9544684 0.79 ALDH1A1 (0.41) TSHRALDH1A1LMNACYP1A2KDM4E
SCHEMBL31299641 0.79 CYP2C9 (0.46) TSHRALDH1A1MEN1KMT2ALMNA
SCHEMBL3541912 0.78 KDM4E (0.49) TSHRALDH1A1MEN1KMT2AHSD17B10
SCHEMBL28353985 0.78 LMNA (0.43) TSHRALDH1A1HSD17B10LMNARAB9A
SCHEMBL9638671 0.77 LMNA (0.43) TSHRALDH1A1MEN1KMT2AHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250075147-A1 FRAGRANCE AND FLAVOR COMPOSITIONS COMPRISING NEW FLAVOR AND FRAGRANCE INGREDIENTS OSMO LABS, PBC 2025-03-06 US claimed
WO-2007086076-A2 AN IMPROVED PROCESS FOR PREPARATION OF LEFLUNOMIDE UNICHEM LABORATORIES LIMITED (IN) 2007-08-02 WO claimed
US-20030139606-A1 Process for preparing 5-methylisoxazole-4-carboxylic- (4'-trifluoromethyl)-anilide RAY ANUP KUMAR (US) 2003-07-24 US claimed
WO-2003042193-A1 PROCESS FOR PREPARING 5-METHYLISOXAZOLE-4-CARBOXYLIC-(4'-TRIFLUOROMETHYL)-ANILIDE GENEVA PHARMACEUTICALS, INC. (US) 2003-05-22 WO claimed
US-20260085048-A1 ACSS2 INHIBITORS AND METHODS OF USE THEREOF EPIVARIO INC (US) 2026-03-26 US disclosed
US-12441689-B2 ACSS2 inhibitors and methods of use thereof EPIVARIO, INC. (US) 2025-10-14 US disclosed
US-20250075147-A1 FRAGRANCE AND FLAVOR COMPOSITIONS COMPRISING NEW FLAVOR AND FRAGRANCE INGREDIENTS OSMO LABS, PBC 2025-03-06 US disclosed
US-20230084752-A1 ACSS2 INHIBITORS AND METHODS OF USE THEREOF METABOMED LTD. (IL) 2023-03-16 US disclosed
EP-3969439-A1 ACSS2 INHIBITORS AND METHODS OF USE THEREOF Metabomed Ltd (IL) 2022-03-23 EP disclosed
CN-110669022-B Micro-channel continuous preparation method of 5-methyl isoxazole-4-formic acid 常州沃腾化工科技有限公司 2022-03-11 CN disclosed
CN-114127049-A ACSS2 inhibitors and methods of use thereof 美特波米德有限公司 2022-03-01 CN disclosed
CN-111233779-B Preparation method of leflunomide 廖文英 2021-08-20 CN disclosed
CN-1015256-B PROCESS FOR PREPARING SUBSTITUTING COMPOUNDS OF BENZYL BUTENYL AMIDO LILLY INDUSTRIES LTD (GB) 1992-01-01 CN disclosed
EP-0257882-B1 N-PHENYL BUTENAMIDES WITH PHARMACEUTICAL PROPERTIES LILLY INDUSTRIES LIMITED (GB) 1991-07-24 EP disclosed
US-4983619-A Leukotriene antagonists LILLY INDUSTRIES LIMITED (GB) 1991-01-08 US disclosed
US-4892963-A IMMUNE DISEASES LILLY INDUSTRIES LIMITED (GB) 1990-01-09 US disclosed
CN-87105515-A Derivatives of phenylbutenamide compounds and preparation method thereof 1988-03-23 CN disclosed
EP-0259972-A2 Heterocyclic propene amide derivatives, processes for their preparation and their use as pharmaceuticals LILLY INDUSTRIES LIMITED (GB) 1988-03-16 EP disclosed
EP-0257882-A1 N-Phenyl butenamides with pharmaceutical properties LILLY INDUSTRIES LIMITED (GB) 1988-03-02 EP disclosed
CN-87105516-A Phenyl crotonamide compound that replaces and preparation method thereof 1988-02-24 CN 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-20230084752-A1 ACSS2 INHIBITORS AND METHODS OF USE THEREOF ACSS2, ADSS2, GLS2 TSHR 3555/4885ALDH1A1 347/4885MEN1 658/4885
US-20260085048-A1 ACSS2 INHIBITORS AND METHODS OF USE THEREOF ACSS2, GLS2, ACSL3 TSHR 1970/4885ALDH1A1 1031/4885MEN1 2249/4885
US-12441689-B2 ACSS2 inhibitors and methods of use thereof ACSS2, ADSS2, GLS2 TSHR 3555/4885ALDH1A1 347/4885MEN1 658/4885
US-20030139606-A1 Process for preparing 5-methylisoxazole-4-carboxylic- (4'-trifluoromethyl)-anilide CA4, ACMSD, CA7 TSHR 627/4885ALDH1A1 46/4885MEN1 4425/4885

“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.