SCHEMBL10341

SCHEMBL10341

Ic1ccc2c(c1)OCCO2

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.48
MAPT P10636 2/20 0.48
HTT P42858 2/20 0.48
BLM P54132 1/20 0.48
ITGB2 P05107 1/20 0.48
ICAM1 P05362 1/20 0.48
ITGAL P20701 1/20 0.48
KDM4E B2RXH2 2/20 0.47
GAA P10253 1/20 0.47
TSHR P16473 1/20 0.45
ALOX5 P09917 1/20 0.45
ADRA2A P08913 1/20 0.44
ADRA2B P18089 1/20 0.44
ADRA2C P18825 1/20 0.44
POLB P06746 1/20 0.42
CRHBP P24387 2/20 0.42
CRHR2 Q13324 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
DYRK1A Q13627 1/20 0.42
DYRK2 Q92630 1/20 0.42

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
SCHEMBL29413018 1.00 LMNA (0.48) LMNAMAPTHTTBLMITGB2
SCHEMBL13182219 0.91 NPC1 (0.44) LMNAMAPTHTTBLMITGB2
SCHEMBL31151216 0.85 CYP3A4 (0.54) MAPTGAAPOLBSMN1; SMN2NPC1
SCHEMBL3117045 0.85 CYP3A4 (0.54) MAPTGAAPOLBSMN1; SMN2NPC1
SCHEMBL29650705 0.79 PRKCI (0.52) MAPTADRA2AADRA2BADRA2CSMN1; SMN2
SCHEMBL1007568 0.79 PRKCI (0.52) MAPTADRA2AADRA2BADRA2CSMN1; SMN2
SCHEMBL1669250 0.76 CHRM2 (0.41) MAPTITGB2ICAM1ITGALADRA2A
SCHEMBL753333 0.76 DYRK1A (0.46) ADRA2AADRA2BADRA2CDYRK1ADYRK2
SCHEMBL29584645 0.76 DYRK1A (0.46) ADRA2AADRA2BADRA2CDYRK1ADYRK2
SCHEMBL3797296 0.76 ACACB (0.36) POLBATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112939829-B Synthetic method of aryl trifluoromethyl thioether 武汉药明康德新药开发有限公司 2023-02-21 CN claimed
CN-112939829-A Synthetic method of aryl trifluoromethyl thioether 武汉药明康德新药开发有限公司 2021-06-11 CN claimed
CN-108017557-B Cyanidation method for preparing nitrile compound 中国科学院兰州化学物理研究所苏州研究院 2020-11-24 CN claimed
US-12624022-B2 Heterocyclic immunomodulators as PDL1 checkpoint inhibitor Janssen Sciences Ireland Unlimited Company (IE) 2026-05-12 US disclosed
EP-4665718-A1 SMALL MOLECULES AS MONOACYLGLYCEROL LIPASE (MAGL) INHIBITORS, COMPOSITIONS AND USE THEREOF Apogee Pharmaceuticals, Inc. (CA) 2025-12-24 EP disclosed
US-12378231-B2 Small molecules as monoacylglycerol lipase (MAGL) inhibitors, compositions and use thereof APOGEE PHARMACEUTICALS, INC. (CA) 2025-08-05 US disclosed
US-20240294514-A1 SMALL MOLECULES AS MONOACYLGLYCEROL LIPASE (MAGL) INHIBITORS, COMPOSITIONS AND USE THEREOF APOGEE PHARMACEUTICALS, INC. (CA) 2024-09-05 US disclosed
WO-2024168426-A1 SMALL MOLECULES AS MONOACYLGLYCEROL LIPASE (MAGL) INHIBITORS, COMPOSITIONS AND USE THEREOF APOGEE PHARMACEUTICALS, INC. (CA) 2024-08-22 WO disclosed
WO-2024129601-A1 COMPOUND EMBODIMENTS FOR MUSCLE MYOSIN INHIBITION AND METHODS OF MAKING AND USING THE SAME BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIV. OF NEVADA (US) 2024-06-20 WO disclosed
EP-3980413-B1 HETEROCYCLIC IMMUNOMODULATORS AS PDL1 CHECKPOINT INHIBITOR JANSSEN SCIENCES IRELAND UNLIMITED CO (IE) 2023-07-19 EP disclosed
EP-3980413-B1 HETEROCYCLIC IMMUNOMODULATORS AS PDL1 CHECKPOINT INHIBITOR JANSSEN SCIENCES IRELAND UNLIMITED CO (IE) 2023-07-19 EP disclosed
EP-1490350-A1 PYRANON AND PYRANDION INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE PFIZER INC. (US) 2004-12-29 EP disclosed
WO-2004081531-A9 LIGAND ANALYSIS NEOGENESIS PHARMACEUTICALS INC (US) 2004-10-28 WO disclosed
WO-2004087156-A1 4-(2-PHENYLSULFANYL-PHENYL)-PIPERIDINE DERIVATIVES AS SEROTONIN REUPTAKE INHIBITORS H. LUNDBECK A/S (DK) 2004-10-14 WO disclosed
WO-2004080463-A1 HETEROCYCLIC KINASE INHIBITORS: METHODS OF USE AND SYNTHESIS SCHERING CORPORATION (US) 2004-09-23 WO disclosed
WO-2004081531-A2 LIGAND ANALYSIS SCHERING CORPORATION (US) 2004-09-23 WO disclosed
WO-2004041789-A1 COMPOSITIONS USEFUL AS INHIBITORS OF JAK AND OTHER PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2004-05-21 WO disclosed
US-20030195239-A1 Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same PFIZER INC. 2003-10-16 US disclosed
WO-2003082848-A1 PYRANON AND PYRANDION INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE PFIZER INC. (US) 2003-10-09 WO disclosed
US-6448433-B1 REACTING AN ORGANIC HALIDE WITH TETRAHYDROXYDIBORON; GROUP 8-11 METAL CATALYST COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANIZATION (AU) 2002-09-10 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-12624022-B2 Heterocyclic immunomodulators as PDL1 checkpoint inhibitor CD274, PDCD1, PDCD1LG2 LMNA 2883/4885MAPT 2477/4885HTT 3885/4885
US-12378231-B2 Small molecules as monoacylglycerol lipase (MAGL) inhibitors, compositions and use thereof MGLL, PNLIP, LPL LMNA 1479/4885MAPT 88/4885HTT 2213/4885
US-20240294514-A1 SMALL MOLECULES AS MONOACYLGLYCEROL LIPASE (MAGL) INHIBITORS, COMPOSITIONS AND USE THEREOF MGLL, PNLIP, LPL LMNA 1479/4885MAPT 88/4885HTT 2213/4885
US-20030195239-A1 Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same POLRMT, RNGTT, RNASE1 LMNA 3489/4885MAPT 2903/4885HTT 4152/4885

“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.