SCHEMBL6097627

SCHEMBL6097627

Cc1ccccc1S(=O)(=O)C(C)C

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.42
MCOLN3 Q8TDD5 1/20 0.42
SLC1A3 P43003 1/20 0.40
SLC1A2 P43004 1/20 0.40
SLC1A1 P43005 1/20 0.40
ALDH1A1 P00352 6/20 0.40
RAPGEF4 Q8WZA2 1/20 0.40
TSHR P16473 1/20 0.39
ACHE P22303 1/20 0.39
EDNRA P25101 2/20 0.39
EDNRB P24530 1/20 0.39
HSD11B1 P28845 2/20 0.39
KDM4E B2RXH2 3/20 0.39
L3MBTL1 Q9Y468 3/20 0.39
TP53 P04637 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
NPSR1 Q6W5P4 2/20 0.38
POLB P06746 1/20 0.38
ADRA2A P08913 1/20 0.38
ADRA1D P25100 1/20 0.38

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
SCHEMBL7504532 0.86 LMNA (0.42) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL8742943 0.84 LMNA (0.41) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL6282158 0.83 SLC1A3 (0.41) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL27492534 0.81 LMNA (0.40) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL562674 0.80 SLC1A3 (0.39) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL31575071 0.80 SLC1A3 (0.39) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL9732243 0.80 KAT6A (0.41) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL7999434 0.78 SLC1A3 (0.38) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL28193048 0.78 CA12 (0.49) LMNAMCOLN3SLC1A3SLC1A2SLC1A1
SCHEMBL4722434 0.77 ADRA2A (0.38) HSD11B1L3MBTL1POLBADRA2AADRA1D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111233823-A Synthesis method of 2-fluoro-1, 3-propane sultone 张家港市国泰华荣化工新材料有限公司 2020-06-05 CN claimed
US-11673130-B2 Catalyst system containing a metathesis catalyst and at least one phenolic compound and a process for metathesis of nitrile-butadiene rubber (NBR) using the catalyst system ARLANXEO DEUTSCHLAND GMBH (DE) 2023-06-13 US disclosed
US-20230137956-A1 ALPHA SUBSTITUTED STAT INHIBITORS AND COMPOSITIONS THEREOF OXFORD FINANCE LLC 2023-05-04 US disclosed
US-20220411426-A1 SUBSTRATE SELECTIVE INHIBITORS OF INSULIN-DEGRADING ENZYME (IDE) AND USES THEREOF PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2022-12-29 US disclosed
EP-3943488-A1 SUBSTITUTED HETEROCYCLIC AMIDE COMPOUND AND PREPARATION METHOD THEREFOR AND PHARMACEUTICAL USE THEREOF Genfleet Therapeutics (Shanghai) Inc. (CN) 2022-01-26 EP disclosed
EP-3372594-B1 PYRIMIDINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER HUMANWELL HEALTHCARE GROUP CO LTD (CN) 2021-07-21 EP disclosed
US-11040976-B2 Substrate selective inhibitors of insulin-degrading enzyme (IDE) and uses thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2021-06-22 US disclosed
WO-2021057867-A1 CLASS OF CDK INHIBITOR BASED ON ORGANIC ARSINE, PREPARATION METHOD AND APPLICATION THEREOF 中国科学院上海有机化学研究所 2021-04-01 WO disclosed
CN-111233823-A Synthesis method of 2-fluoro-1, 3-propane sultone 张家港市国泰华荣化工新材料有限公司 2020-06-05 CN disclosed
WO-2020018788-A1 DEGRADERS THAT TARGET PROTEINS VIA KEAP1 DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-01-23 WO disclosed
US-20150309348-A1 OPTICAL FILM, OPTICAL COMPENSATION FILM, POLARIZING PLATE AND LIQUID CRYSTAL DISPLAY FUJIFILM CORPORATION (JP) 2015-10-29 US disclosed
US-20140128387-A1 CERTAIN PROTEIN KINASE INHIBITORS SHANGHAI iNSTITUTE OF MATERIA MEDICA ACADEMY OF SCIENCES (CN) 2014-05-08 US disclosed
US-20110059951-A1 HETEROCYCLIC DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS INCYTE CORPORATION 2011-03-10 US disclosed
US-7550458-B2 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY (US) 2009-06-23 US disclosed
US-7550458-B2 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY (US) 2009-06-23 US disclosed
US-20070088029-A1 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY 2007-04-19 US disclosed
US-20070088029-A1 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY 2007-04-19 US disclosed
US-20070078146-A1 Antiinflamamtory agents; antiarthritic agents; inflammatory bowel disorders; multiple sclerosis; asthma PHARMACIA CORPORATION 2007-04-05 US disclosed
US-7101892-B2 Sulfone derivatives as 5-HT7 receptor ligands MERCK SHARP & DOHME LTD. 2006-09-05 US disclosed
US-20040229864-A1 Sulfone derivatives as 5-HT7 receptor ligands MERCK SHARP & DOHME LTD. (GB) 2004-11-18 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 (8 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-20040229864-A1 Sulfone derivatives as 5-HT7 receptor ligands HTR7, HTR2C, HTR1A LMNA 3190/4885MCOLN3 2536/4885SLC1A3 544/4885
US-20110059951-A1 HETEROCYCLIC DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS JAK3, JAK1, JAK2 LMNA 4745/4885MCOLN3 3396/4885SLC1A3 3974/4885
US-20220411426-A1 SUBSTRATE SELECTIVE INHIBITORS OF INSULIN-DEGRADING ENZYME (IDE) AND USES THEREOF IDE, SI, GPR119 LMNA 2054/4885MCOLN3 3840/4885SLC1A3 2166/4885
US-20230137956-A1 ALPHA SUBSTITUTED STAT INHIBITORS AND COMPOSITIONS THEREOF STAT5A, STAT5B, STAT3 LMNA 4588/4885MCOLN3 4415/4885SLC1A3 4766/4885
US-20070078146-A1 Antiinflamamtory agents; antiarthritic agents; inflammatory bowel disorders; multiple sclerosis; asthma MAPK1, MAPK3, MAPK4 LMNA 4386/4885MCOLN3 2167/4885SLC1A3 3612/4885
US-20140128387-A1 CERTAIN PROTEIN KINASE INHIBITORS PRKACA, PRKDC, PRKACB LMNA 2830/4885MCOLN3 4701/4885SLC1A3 3998/4885
US-11040976-B2 Substrate selective inhibitors of insulin-degrading enzyme (IDE) and uses thereof IDE, SI, GPR119 LMNA 2131/4885MCOLN3 3615/4885SLC1A3 1906/4885
US-20070088029-A1 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function VDR, ESRRB, NR5A1 LMNA 3299/4885MCOLN3 2624/4885SLC1A3 4549/4885

“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.