SCHEMBL1504601

SCHEMBL1504601

Cc1ccc(S(=O)(=O)NCCCl)cc1

nearest known ligand 0.66

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 10/20 0.66
KMT2A Q03164 2/20 0.66
MEN1 O00255 1/20 0.66
CA12 O43570 2/20 0.60
CA9 Q16790 2/20 0.60
CA2 P00918 1/20 0.60
LMNA P02545 1/20 0.58
HPGD P15428 1/20 0.58
HTT P42858 1/20 0.58
ALOX15 P16050 1/20 0.58
GAA P10253 2/20 0.57
L3MBTL1 Q9Y468 2/20 0.54
GBA1 P04062 1/20 0.54
CYP1A2 P05177 1/20 0.54
CYP3A4 P08684 1/20 0.54
ATM Q13315 1/20 0.54
MBTD1 Q05BQ5 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.53
CYP19A1 P11511 1/20 0.53

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
SCHEMBL9876657 0.89 ALDH1A1 (0.70) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL5567042 0.88 ALDH1A1 (0.75) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL8213969 0.86 ALDH1A1 (0.72) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7201051 0.84 ALDH1A1 (0.86) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7094852 0.84 ALDH1A1 (0.79) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL2627771 0.84 ALDH1A1 (0.68) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7093365 0.82 ALDH1A1 (0.77) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7097551 0.82 ALDH1A1 (0.77) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7092896 0.82 ALDH1A1 (0.77) ALDH1A1KMT2AMEN1CA12CA9
SCHEMBL7095193 0.82 ALDH1A1 (0.77) ALDH1A1KMT2AMEN1CA12CA9

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-119638643-A Iron death inhibitor targeting endoplasmic reticulum as well as preparation method and application thereof 山东中医药大学附属医院 2025-03-18 CN claimed
CN-111073279-A Formula and preparation method of nylon pipe with high pressure-bearing capacity 无锡殷达尼龙有限公司 2020-04-28 CN claimed
CN-111004503-A Formula of nylon hose material 无锡殷达尼龙有限公司 2020-04-14 CN claimed
EP-0789699-B1 SPIRO[HETEROCYCLE-IMIDAZO[1,2-a]INDENO[1,2-e]PYRAZINE]-4'-ONES, PREPARATION THEREOF AND DRUGS CONTAINING SAME RHONE POULENC RORER SA (FR) 1999-03-17 EP claimed
CN-119638643-A Iron death inhibitor targeting endoplasmic reticulum as well as preparation method and application thereof 山东中医药大学附属医院 2025-03-18 CN disclosed
CN-115843271-B Indole derivatives and their use for the treatment of cancer 克洛德贝纳尔-里昂第一大学 2024-08-13 CN disclosed
US-20230278983-A1 INDOLE DERIVATIVES AND USES THEREOF FOR TREATING A CANCER UNIVERSITE CLAUDE BERNARD LYON 1 (FR) 2023-09-07 US disclosed
US-20230278983-A1 INDOLE DERIVATIVES AND USES THEREOF FOR TREATING A CANCER UNIVERSITE CLAUDE BERNARD LYON 1 (FR) 2023-09-07 US disclosed
CN-115843271-A Indole derivatives and their use for the treatment of cancer 克洛德贝纳尔-里昂第一大学 2023-03-24 CN disclosed
EP-2423201-B1 Luminescent macrocyclic lanthanide complexes UNIV CALIFORNIA (US) 2017-10-04 EP disclosed
US-9556122-B2 Luminescent 1-hydroxy-2-pyridinone chelates of lanthanides THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2017-01-31 US disclosed
CN-102459197-B Be applicable to treatment response thrombotonin 5-HT 6n-phenyl-(piperazinyl or homopiperazine the base)-benzsulfamide of the illness of the adjustment of acceptor or benzenesulfonyl-phenyl-(piperazine or homopiperazine) compound ABBVIE (US) 2015-08-19 CN disclosed
WO-2011033009-A1 N- [2-HYDROXYCARBAMOYL-2- (PIPERAZINYL) ETHYL] BENZAMIDE COMPOUNDS, THEIR PREPARATION AND THEIR USE AS TACE INHIBITORS GALDERMA RESEARCH & DEVELOPMENT (FR) 2011-03-24 WO disclosed
US-20100015725-A1 LUMINESCENT 1-HYDROXY-2-PYRIDINONE CHELATES OF LANTHANIDES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2010-01-21 US disclosed
US-20100015725-A1 LUMINESCENT 1-HYDROXY-2-PYRIDINONE CHELATES OF LANTHANIDES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2010-01-21 US disclosed
US-20090143582-A1 Process for making n-(diphenylmethyl)piperazines SYNTHON BV (NL) 2009-06-04 US disclosed
US-20090098074-A1 Keratin-Binding Effector Molecules Containing Reactive Dyes BASF SE (DE) 2009-04-16 US disclosed
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 US disclosed
US-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-09-04 US disclosed
WO-2008063721-A2 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2008-05-29 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 (5 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-20080213917-A1 LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES SSB, HACD3, CLTA ALDH1A1 4586/4885KMT2A 3655/4885MEN1 1772/4885
US-20090098074-A1 Keratin-Binding Effector Molecules Containing Reactive Dyes KRT18, KLK3, KLKB1 ALDH1A1 2661/4885KMT2A 2796/4885MEN1 4346/4885
US-20230278983-A1 INDOLE DERIVATIVES AND USES THEREOF FOR TREATING A CANCER CSNK2A1, IDO1, CSNK2A3 ALDH1A1 995/4885KMT2A 574/4885MEN1 2477/4885
US-20100015725-A1 LUMINESCENT 1-HYDROXY-2-PYRIDINONE CHELATES OF LANTHANIDES PLPBP, HPD, LASP1 ALDH1A1 411/4885KMT2A 3670/4885MEN1 1167/4885
US-20090143582-A1 Process for making n-(diphenylmethyl)piperazines CYP51A1, CYP3A5, CYP4Z1 ALDH1A1 2312/4885KMT2A 659/4885MEN1 3940/4885

“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.