SCHEMBL70071

SCHEMBL70071

COC(=O)c1cccc(C(C)=O)c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.59
RAB9A P51151 4/20 0.59
LOXL2 Q9Y4K0 1/20 0.58
CREBBP Q92793 1/20 0.57
ALDH1A1 P00352 1/20 0.57
CYP4F2 P78329 2/20 0.56
CYP4A11 Q02928 2/20 0.56
NPC1 O15118 3/20 0.56
POLB P06746 1/20 0.54
MAPT P10636 2/20 0.53
TP53 P04637 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
SLC7A5 Q01650 1/20 0.53
CA12 O43570 1/20 0.52
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
CA7 P43166 1/20 0.52
XDH P47989 1/20 0.52
CA9 Q16790 1/20 0.52
CA14 Q9ULX7 1/20 0.52

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
SCHEMBL29585950 1.00 TSHR (0.59) TSHRRAB9ALOXL2CREBBPALDH1A1
Acetone SCHEMBL27885920 0.91 TSHR (0.64) TSHRRAB9ALOXL2ALDH1A1CYP4F2
SCHEMBL34953 0.91 TSHR (0.70) TSHRRAB9ALOXL2ALDH1A1CYP4F2
SCHEMBL17348229 0.90 CA12 (0.60) TSHRRAB9ALOXL2ALDH1A1CYP4F2
Methyl Alcohol SCHEMBL28469619 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2
Ammonia Solution, Strong SCHEMBL28556515 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2
Potassium SCHEMBL30190417 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2
SCHEMBL29966404 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2
SCHEMBL10941453 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2
SCHEMBL8054504 0.89 TSHR (0.67) TSHRRAB9ALOXL2ALDH1A1CYP4F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118879796-A Method for synthesizing methyl salicylate compound by taking biological enzyme as catalyst 济南大学 2024-11-01 CN claimed
CN-118240886-A Method for synthesizing ethyl salicylate compound by biological enzyme catalysis 济南大学 2024-06-25 CN claimed
CN-109134222-B Preparation method of 2-hydroxy isopropyl substituted acetophenone 上海博栋化学科技有限公司 2022-01-21 CN claimed
CN-109134222-A A kind of preparation method for the acetophenone that 2- hydroxyisopropyl replaces 上海博栋化学科技有限公司 2019-01-04 CN claimed
US-20260108482-A1 MODULATORS OF MAS-RELATED G-PROTEIN RECEPTOR X4 AND RELATED PRODUCTS AND METHODS ESCIENT PHARMACEUTICALS INC (US) 2026-04-23 US disclosed
CN-115066428-B Boric acid derivatives 首药控股(北京)股份有限公司 2025-06-13 CN disclosed
CN-119241504-A Spiroindoline inhibitors of KIF18A 沃拉斯查疗法公司 2025-01-03 CN disclosed
EP-3615525-B1 PYRROLE DERIVATIVES AS PLK1 INHIBITORS SENTINEL ONCOLOGY LTD (GB) 2024-12-25 EP disclosed
US-20240351984-A1 INDOLINE COMPOUNDS FOR INHIBITING KIF18A VOLASTRA THERAPEUTICS, INC. (US) 2024-10-24 US disclosed
EP-3800186-B1 CYANOPYRROLIDINES AS DUB INHIBITORS FOR THE TREATMENT OF CANCER MISSION THERAPEUTICS LTD (GB) 2024-10-02 EP disclosed
CN-114450271-B Ureas, amino and substituted heteroaryl compounds for Cbl-b inhibition 纽力克斯治疗公司 2024-09-20 CN disclosed
WO-2024191268-A1 NOVEL COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME 현대약품 주식회사 2024-09-19 WO disclosed
WO-2001085723-A1 GASTRIN AND CHOLECYSTOKININ RECEPTOR LIGANDS (II) JAMES BLACK FOUNDATION LIMITED (GB) 2001-11-15 WO disclosed
EP-0509769-B1 Heterocyclic amides having HLE inhibiting activity ZENECA LTD (GB) 1996-09-11 EP disclosed
US-5521179-A Heterocyclic amides ZENECA LIMITED (GB) 1996-05-28 US disclosed
WO-1996004282-A1 CARBAPENEM COMPOUNDS, COMPOSITIONS AND METHODS OF TREATMENT MERCK & CO., INC. (US) 1996-02-15 WO disclosed
EP-0509769-A2 Heterocyclic amides having HLE inhibiting activity ZENECA LIMITED (GB) 1992-10-21 EP disclosed
EP-0083228-B1 PHARMACEUTICALLY ACTIVE PHENYLCARBOXYLIC ACID DERIVATIVES ICI AMERICAS INC. (US) 1985-05-15 EP disclosed
US-4499299-A Pharmaceutically active phenylcarboxylic acid derivatives ICI AMERICAS INC. (US) 1985-02-12 US disclosed
EP-0083228-A1 Pharmaceutically active phenylcarboxylic acid derivatives ICI AMERICAS INC. (US) 1983-07-06 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-20240351984-A1 INDOLINE COMPOUNDS FOR INHIBITING KIF18A KIF18A, KIF18B, KIF2C TSHR 4541/4885RAB9A 258/4885LOXL2 4140/4885
US-20260108482-A1 MODULATORS OF MAS-RELATED G-PROTEIN RECEPTOR X4 AND RELATED PRODUCTS AND METHODS MRGPRX4, MRGPRX1, MRGPRX2 TSHR 34/4885RAB9A 665/4885LOXL2 2908/4885

“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.