SCHEMBL436002

SCHEMBL436002

CS(=O)(=O)OCC1CCN(S(C)(=O)=O)CC1

nearest known ligand 0.44

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.44
CYP4F2 P78329 1/20 0.40
CYP4A11 Q02928 1/20 0.40
L3MBTL1 Q9Y468 2/20 0.40
HTT P42858 2/20 0.40
ALDH1A1 P00352 4/20 0.38
ATM Q13315 1/20 0.38
NPSR1 Q6W5P4 1/20 0.37
FABP6 P51161 1/20 0.37
TSHR P16473 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
POLB P06746 1/20 0.36
GPR119 Q8TDV5 1/20 0.36
ALOX5AP P20292 1/20 0.35
FEN1 P39748 1/20 0.35
BRD4 O60885 1/20 0.33

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
SCHEMBL20323506 0.87 MAPT (0.40) TP53L3MBTL1ALDH1A1TSHRPOLB
SCHEMBL20323505 0.85 ALDH1A1 (0.35) TP53CYP4F2CYP4A11ALDH1A1TSHR
SCHEMBL13752703 0.82 NCF1 (0.43) ALDH1A1TSHR
SCHEMBL12522316 0.82 TP53 (0.50) TP53CYP4F2CYP4A11L3MBTL1HTT
SCHEMBL20300385 0.81 ALDH1A1 (0.43) TP53CYP4F2CYP4A11L3MBTL1HTT
SCHEMBL14414058 0.81 USP2 (0.42) ALDH1A1TSHR
SCHEMBL7705221 0.81 USP2 (0.42) ALDH1A1TSHR
SCHEMBL1062380 0.81
SCHEMBL16127663 0.81 TP53 (0.44) TP53CYP4F2CYP4A11L3MBTL1HTT
SCHEMBL15387041 0.81 TP53 (0.44) TP53CYP4F2CYP4A11L3MBTL1HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240158378-A1 SOLID FORMS OF A 4H-PYRAN-4-ONE STRUCTURED CYP11A1 INHIBITOR ORION CORPORATION (FI) 2024-05-16 US claimed
EP-4301749-A1 SOLID FORMS OF A 4H-PYRAN-4-ONE STRUCTURED CYP11A1 INHIBITOR Orion Corporation (FI) 2024-01-10 EP claimed
WO-2022184977-A1 SOLID FORMS OF A 4H-PYRAN-4-ONE STRUCTURED CYP11A1 INHIBITOR ORION CORPORATION (FI) 2022-09-09 WO claimed
WO-2025051216-A1 CYP11A1 INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF 深圳众格生物科技有限公司 2025-03-13 WO disclosed
CN-119330948-A CYP11A1 inhibitor and application thereof 西藏海思科制药有限公司 2025-01-21 CN disclosed
CN-119330947-A CYP11A1 inhibitor and application thereof 西藏海思科制药有限公司 2025-01-21 CN disclosed
US-20250011285-A1 CYP11A1 INHIBITORS ORION CORPORATION (FI) 2025-01-09 US disclosed
WO-2024217531-A1 CYP11A1 INHIBITORS AND USE THEREOF 西藏海思科制药有限公司 2024-10-24 WO disclosed
US-20240336603-A1 PROCESS FOR THE PREPARATION OF A CYP11A1 INHIBITOR AND INTERMEDIATES THEREOF ORION CORPORATION (FI) 2024-10-10 US disclosed
WO-2024199421-A1 CYP11A1 INHIBITOR 山东轩竹医药科技有限公司 2024-10-03 WO disclosed
EP-4430027-A1 CYP11A1 INHIBITORS Orion Corporation (FI) 2024-09-18 EP disclosed
WO-2013144097-A1 NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACID DERIVATIVES AND THEIR USE AS GPR40 RECEPTOR AGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-10-03 WO disclosed
US-20130252937-A1 NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-09-26 US disclosed
US-20130252937-A1 NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-09-26 US disclosed
WO-2012011707-A2 SUBSTITUTED PYRIDINONE DERIVATIVES AND METHODS FOR MANUFACTURING THE SAME HYUNDAI PHARM CO., LTD. (KR) 2012-01-26 WO disclosed
US-20060142336-A1 N-sulfonylpiperidines as metalloproteinase inhibitors (tace) ASTRAZENECA AB (SE) 2006-06-29 US disclosed
US-20060063783-A1 Sulphonylpiperidine derivatives containing an alkenyl or alkynyl moiety for use as matrix metalloproteinase inhibitors ASTRAZENECA AB (GB) 2006-03-23 US disclosed
CN-1668302-A Sulphonylpiperidine derivatives containing an alkenyl or alkynly moiety for use as matrix metalloproteinase inhibitors ASTRAZENECA AB (SE) 2005-09-14 CN disclosed
EP-1531821-A2 SULPHONYLPIPERIDINE DERIVATIVES CONTAINING AN ALKENYL OR ALKYNYL MOIETY FOR USE AS MATRIX METALLOPROTEINASE INHIBITORS Astrazeneca AB (SE) 2005-05-25 EP disclosed
WO-2004006927-A2 SULPHONYLPIPERIDINE DERIVATIVES CONTAINING AN ALKENYL OR ALKYNLY MOIETY FOR USE AS MATRIX METALLOPROTEINASE INHIBITORS ASTRAZENECA AB (SE) 2004-01-22 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 (6 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-20250011285-A1 CYP11A1 INHIBITORS CYP11B1, CYP19A1, CYP11B2 TP53 923/4885CYP4F2 46/4885CYP4A11 5/4885
US-20060063783-A1 Sulphonylpiperidine derivatives containing an alkenyl or alkynyl moiety for use as matrix metalloproteinase inhibitors MMP9, MMP2, TIMP3 TP53 2027/4885CYP4F2 2745/4885CYP4A11 2019/4885
US-20240336603-A1 PROCESS FOR THE PREPARATION OF A CYP11A1 INHIBITOR AND INTERMEDIATES THEREOF CYP11B1, CYP4A11, CYP19A1 TP53 1834/4885CYP4F2 20/4885CYP4A11 2/4885
US-20130252937-A1 NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS GPR119, GPR55, GPR52 TP53 3515/4885CYP4F2 178/4885CYP4A11 609/4885
US-20240158378-A1 SOLID FORMS OF A 4H-PYRAN-4-ONE STRUCTURED CYP11A1 INHIBITOR CYP2S1, CYP19A1, CYP4A11 TP53 541/4885CYP4F2 28/4885CYP4A11 3/4885
US-20060142336-A1 N-sulfonylpiperidines as metalloproteinase inhibitors (tace) ADAM10, ADAM9, CTRL TP53 2758/4885CYP4F2 2274/4885CYP4A11 354/4885

“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.