SCHEMBL34841

SCHEMBL34841

O=C(O)c1cccc(S(=O)(=O)N2CCOCC2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.76
IL1RN P18510 1/20 0.76
TSHR P16473 1/20 0.75
RECQL P46063 1/20 0.75
APEX1 P27695 1/20 0.68
ALB P02768 1/20 0.67
MAPK1 P28482 1/20 0.66
NPC1 O15118 1/20 0.66
GAA P10253 1/20 0.66
AKR1C3 P42330 2/20 0.63
ALDH1A1 P00352 1/20 0.63
AKR1C1 Q04828 1/20 0.63
MEN1 O00255 1/20 0.62
KMT2A Q03164 1/20 0.62

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
SCHEMBL30005696 1.00 MAPT (0.76) MAPTIL1RNTSHRRECQLAPEX1
SCHEMBL28283475 0.90 TSHR (0.77) TSHRRECQLMAPK1NPC1GAA
SCHEMBL15773014 0.87 TSHR (0.73) TSHRRECQLMAPK1NPC1GAA
SCHEMBL7321050 0.87 KMT2A (0.80) MAPTTSHRRECQLMAPK1ALDH1A1
SCHEMBL2850336 0.87 GAA (0.74) TSHRRECQLMAPK1NPC1GAA
SCHEMBL3932198 0.86 MAPT (0.94) MAPTIL1RNTSHRAPEX1NPC1
SCHEMBL29463849 0.86 MAPT (1.00) MAPTIL1RNTSHRAPEX1NPC1
SCHEMBL1001486 0.86 MAPT (1.00) MAPTIL1RNTSHRAPEX1NPC1
SCHEMBL1001537 0.85 MAPT (0.97) MAPTIL1RNTSHRAPEX1NPC1
SCHEMBL30213397 0.85 MAPT (0.97) MAPTIL1RNTSHRAPEX1NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3551633-B1 SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS LEO PHARMA AS (DK) 2021-03-31 EP claimed
EP-3551634-A1 SUBSTITUTED PYRAZOLOAZEPIN-8-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS Leo Pharma A/S (DK) 2019-10-16 EP claimed
CN-110099905-A SUBSTITUTED PYRAZOLOAZEPIN-8-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS 利奥制药有限公司 2019-08-06 CN claimed
CN-110088108-A SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS 利奥制药有限公司 2019-08-02 CN claimed
WO-2018108231-A1 SUBSTITUTED PYRAZOLOAZEPIN-8-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS LEO PHARMA A/S (DK) 2018-06-21 WO claimed
EP-1615904-B1 SUBSTITUTED BENZOSULPHONAMIDES AS POTENTIATORS OF GLUTAMATE RECEPTORS ASTRAZENECA AB (SE) 2008-02-27 EP claimed
US-4029787-A Basically substituted 3-sulfamoylbenzoic acid derivatives and process for their preparation HOECHST AKTIENGESELLSCHAFT (DT) 1977-06-14 US claimed
EP-4737451-A1 NOVEL CARBOXAMIDE DERIVATIVE COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME Dong Wha Pharm. Co., Ltd. (KR) 2026-05-06 EP disclosed
WO-2025003988-A1 NOVEL CARBOXAMIDE DERIVATIVE COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME 동화약품주식회사 2025-01-02 WO disclosed
US-20240018242-A1 METHODS OF TREATING CANCER USING LSD1 INHIBITORS IN COMBINATION WITH IMMUNOTHERAPY CHILDREN'S MEDICAL CENTER CORPORATION 2024-01-18 US disclosed
EP-4219689-A2 IMMUNE EFFECTOR CELL THERAPIES WITH ENHANCED EFFICACY Novartis AG (CH) 2023-08-02 EP disclosed
US-11685782-B2 Methods of treating cancer using LSD1 inhibitors in combination with immunotherapy CHILDREN'S MEDICAL CENTER CORPORATION (US) 2023-06-27 US disclosed
EP-3397756-B1 IMMUNE EFFECTOR CELL THERAPIES WITH ENHANCED EFFICACY NOVARTIS AG (CH) 2023-03-08 EP disclosed
US-20040142981-A1 Antibacterial benzoic acid derivatives PHARMACIA & UPJOHN COMPANY 2004-07-22 US disclosed
WO-2004018414-A2 ANTIBACTERIAL AGENTS PHARMACIA & UPJOHN COMPANY LLC (US) 2004-03-04 WO disclosed
WO-2004018461-A2 ANTIBACTERIAL BENZOIC ACID DERIVATIVES PHARMACIA & UPJOHN COMPANY LLC (US) 2004-03-04 WO disclosed
WO-2004007498-A2 3-PHENYL ANALOGS OF TOXOFLAVINE AS KINASE INHIBITORS JANSSEN PHARMACEUTICA N.V. (BE) 2004-01-22 WO disclosed
US-20020111369-A1 Aryl sulfonic acids and derivatives as FSH antagonists AMERICAN HOME PRODUCTS CORPORATION (US) 2002-08-15 US disclosed
US-6355633-B1 CONTRACEPTIVES AMERICAN HOME PRODUCTS CORPORATION 2002-03-12 US disclosed
WO-2000058277-A1 ARYL SULFONIC ACIDS AND DERIVATIVES AS FSH ANTAGONISTS AMERICAN HOME PRODUCTS CORPORATION (US) 2000-10-05 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 (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-11685782-B2 Methods of treating cancer using LSD1 inhibitors in combination with immunotherapy KDM1B, KDM2A, KDM3B MAPT 3200/4885IL1RN 1104/4885TSHR 4077/4885
US-20020111369-A1 Aryl sulfonic acids and derivatives as FSH antagonists FSHR, GNRHR, LHCGR MAPT 4858/4885IL1RN 1414/4885TSHR 29/4885
US-20040142981-A1 Antibacterial benzoic acid derivatives GABRD, PHB1, GABBR1 MAPT 4754/4885IL1RN 790/4885TSHR 3901/4885
US-20240018242-A1 METHODS OF TREATING CANCER USING LSD1 INHIBITORS IN COMBINATION WITH IMMUNOTHERAPY KDM1B, KDM2A, KDM3B MAPT 3200/4885IL1RN 1104/4885TSHR 4077/4885

“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.