SCHEMBL136005

SCHEMBL136005

O=C(Cl)OCc1ccc(F)cc1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.64
MMP1 P03956 1/20 0.49
MMP2 P08253 1/20 0.49
MMP9 P14780 1/20 0.49
MMP12 P39900 1/20 0.49
IDO1 P14902 2/20 0.48
AGXT P21549 2/20 0.48
NR4A2 P43354 1/20 0.47
MAPT P10636 2/20 0.46
KDM4E B2RXH2 1/20 0.46
LMNA P02545 1/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
FABP7 O15540 1/20 0.46
FABP5 Q01469 1/20 0.46
MAOB P27338 2/20 0.46
PARP10 Q53GL7 1/20 0.46
CYP1A2 P05177 1/20 0.44

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
SCHEMBL8021350 0.89 ALDH1A1 (0.78) ALDH1A1MMP1MMP2MMP9MMP12
SCHEMBL6554287 0.83 IDO1 (0.52) MMP1MMP2MMP9MMP12IDO1
SCHEMBL1788919 0.83 KDM4E (0.53) MMP1MMP2MMP9MMP12IDO1
SCHEMBL1788921 0.81 NR4A2 (0.53) ALDH1A1MMP1MMP2MMP9MMP12
SCHEMBL137476 0.81 ALDH1A1 (0.67) ALDH1A1MMP1MMP2MMP9MMP12
SCHEMBL12992908 0.81 ALDH1A1 (0.67) ALDH1A1LMNAMEN1KMT2ASMN1; SMN2
SCHEMBL7303745 0.80 HRH3 (0.46) ALDH1A1MMP1MMP2MMP9MMP12
SCHEMBL3936532 0.80 LMNA (0.43) ALDH1A1KDM4ELMNA
SCHEMBL6556972 0.79 ALDH1A1 (0.64) ALDH1A1MMP1MMP2MMP9MMP12
SCHEMBL11571335 0.79 ALDH1A1 (0.64) ALDH1A1IDO1MEN1KMT2AHRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250387403-A1 SELECTIVE SIGMA-2 RECEPTOR LIGANDS AS MODULATORS OF TMEM97 UNIV TEXAS (US) 2025-12-25 US disclosed
EP-4525879-A2 SELECTIVE SIGMA-2 RECEPTOR LIGANDS AS MODULATORS OF TMEM97 Board of Regents, The University of Texas System (US) 2025-03-26 EP disclosed
CN-117164462-B Diaryl methane compound and preparation method and application thereof 江西师范大学 2024-10-18 CN disclosed
CN-117164462-A Diaryl methane compound and preparation method and application thereof 江西师范大学 2023-12-05 CN disclosed
WO-2023225563-A2 SELECTIVE SIGMA-2 RECEPTOR LIGANDS AS MODULATORS OF TMEM97 BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2023-11-23 WO disclosed
CN-108779096-B Fluorine-substituted cyclopropylamine compounds, and preparation method, pharmaceutical composition and application thereof 中国科学院上海药物研究所 2022-07-01 CN disclosed
US-10836743-B2 Fluorinated cyclopropylamine compound, preparation method therefor, pharmaceutical composition thereof, and uses thereof SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2020-11-17 US disclosed
EP-3486231-B1 PYRROLIDINE DERIVATIVE SERVING AS PPAR AGONIST GUANGDONG RAYNOVENT BIOTECH CO LTD (CN) 2020-05-20 EP disclosed
US-20190225597-A1 PYRROLIDINE DERIVATIVES AS PPAR AGONISTS Guangdong Raynovent Biotech Co., Ltd. (CN) 2019-07-25 US disclosed
EP-3486231-A1 PYRROLIDINE DERIVATIVE SERVING AS PPAR AGONIST Guangdong Raynovent Biotech Co., Ltd. (CN) 2019-05-22 EP disclosed
WO-1997049668-A1 INHIBITIORS OF CYSTEINE PROTEASE SMITHKLINE BEECHAM CORPORATION (US) 1997-12-31 WO disclosed
US-5436242-A Tetrahydrothienopyridine derivatives, furo and pyrrolo analogs thereof for inhibiting blood platelet aggregation SANKYO COMPANY, LIMITED (JP) 1995-07-25 US disclosed
US-5288726-A Tetrahydrothienopyridine derivatives, furo and pyrrolo analogs thereof and their preparation and uses for inhibiting blood platelet aggregation UBE INDUSTRIES LIMITED (JP) 1994-02-22 US disclosed
US-5254558-A Substituted 1,3-diazines as leukocyte elastase inhibitors IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-10-19 US disclosed
EP-0542411-A2 Tetrahydrothienopyridine derivatives, furo and pyrrolo analogs thereof and their preparation and uses for inhibiting blood platelet aggregation Sankyo Company Limited (JP) 1993-05-19 EP disclosed
EP-0237522-B1 PHARMACEUTICALLY ACTIVE DERIVATIVES OF TRYPTOPHAN AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1993-02-24 EP disclosed
EP-0528633-A1 Pyrimidinyl acetamides as elastase inhibitors ZENECA LIMITED (GB) 1993-02-24 EP disclosed
US-4870097-A ANALGESICS, CENTRAL NERVOUS SYSTEM DISORDERS ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1989-09-26 US disclosed
EP-0237522-A1 PHARMACEUTICALLY ACTIVE DERIVATIVES OF TRYPTOPHAN AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. ROTTA RESEARCH LAB (IT) 1987-09-23 EP disclosed
WO-1986003489-A1 PHARMACEUTICALLY ACTIVE DERIVATIVES OF TRYPTOPHAN AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1986-06-19 WO 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 (3 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-20250387403-A1 SELECTIVE SIGMA-2 RECEPTOR LIGANDS AS MODULATORS OF TMEM97 TMEM97, SIGMAR1, OPRL1 ALDH1A1 1645/4885MMP1 4774/4885MMP2 4723/4885
US-20190225597-A1 PYRROLIDINE DERIVATIVES AS PPAR AGONISTS PPARD, PPARA, PPARG ALDH1A1 1866/4885MMP1 741/4885MMP2 2595/4885
US-10836743-B2 Fluorinated cyclopropylamine compound, preparation method therefor, pharmaceutical composition thereof, and uses thereof SETDB1, KDM1B, SETD7 ALDH1A1 354/4885MMP1 3456/4885MMP2 3165/4885

“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.