SCHEMBL91188

SCHEMBL91188

CCc1cccc(OCc2ccccc2)c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 5/20 0.68
BCHE P06276 7/20 0.66
CYP4F2 P78329 1/20 0.64
CYP4A11 Q02928 1/20 0.64
SOD1 P00441 1/20 0.58
MAOA P21397 1/20 0.57
NR4A2 P43354 1/20 0.57
ALOX5 P09917 1/20 0.56
LCK P06239 1/20 0.54
KDM4E B2RXH2 1/20 0.54
MEN1 O00255 1/20 0.54
ALDH1A1 P00352 1/20 0.54
GAA P10253 1/20 0.54
MAPT P10636 1/20 0.54
THRB P10828 1/20 0.54
PKM P14618 1/20 0.54
RAB9A P51151 1/20 0.54
BLM P54132 1/20 0.54
KMT2A Q03164 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54

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
SCHEMBL29925214 1.00 MAOB (0.68) MAOBBCHECYP4F2CYP4A11SOD1
Methylamine SCHEMBL9454395 0.96 MAOB (0.64) MAOBBCHECYP4F2CYP4A11SOD1
Formaldehyde SCHEMBL27752554 0.95 MAOB (0.62) MAOBBCHECYP4F2CYP4A11SOD1
SCHEMBL13462828 0.92 MAOB (0.58) MAOBBCHECYP4F2CYP4A11SOD1
SCHEMBL3918721 0.89 MAOB (0.58) MAOBBCHECYP4F2CYP4A11SOD1
Acetic Acid Methyl Ester SCHEMBL28085683 0.87 MAOB (0.62) MAOBBCHECYP4F2CYP4A11NR4A2
SCHEMBL13753986 0.86 MAOB (0.59) MAOBBCHECYP4F2CYP4A11MAOA
SCHEMBL13463060 0.86 SMN1; SMN2 (0.57) MAOBBCHECYP4F2CYP4A11SOD1
SCHEMBL13462938 0.86 MAOB (0.65) MAOBBCHERAB9A
SCHEMBL13462917 0.86 MAOB (0.60) MAOBBCHECYP4F2CYP4A11SOD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025235719-A1 DIMERIC SMAC MIMETICS USEFUL IN HIV THERAPY VIIV HEALTHCARE COMPANY (US) 2025-11-13 WO disclosed
WO-2025217560-A1 TRIAZOLO INDAZOLE COMPOUNDS AS JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2025-10-16 WO disclosed
US-12398135-B2 Dimethyl amino azetidine amides as JAK inhibitors THERAVANCE BIOPHARMA R&D IP, LLC (US) 2025-08-26 US disclosed
US-20250034131-A1 DIMETHYL AMINO AZETIDINE AMIDES AS JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP LLC (US) 2025-01-30 US disclosed
EP-4114836-B1 CRYSTALLINE HYDRATE OF A JAK INHIBITOR COMPOUND THERAVANCE BIOPHARMA R&D IP LLC (US) 2025-01-08 EP disclosed
US-12122773-B2 Crystalline hydrate of a JAK inhibitor compound THERAVANCE BIOPHARMA R&D IP, LLC (US) 2024-10-22 US disclosed
EP-3837258-B1 DIMETHYL AMINO AZETIDINE AMIDES AS JAK INHIBITORS THERAVANCE BIOPHARMA R&D IP LLC (US) 2024-04-24 EP disclosed
US-20240025897-A1 CRYSTALLINE HYDRATE OF A JAK INHIBITOR COMPOUND THERAVANCE BIOPHARMA R&D IP LLC (US) 2024-01-25 US disclosed
WO-2023205701-A1 MACROCYCLIC HETEROCYCLES AND USES THEREOF KUMQUAT BIOSCIENCES INC. (US) 2023-10-26 WO disclosed
CN-112703037-B 5-to 7-membered heterocyclic amides as JAK inhibitors 施万生物制药研发IP有限责任公司 2023-10-20 CN disclosed
US-5840684-A Glycopeptide antibiotic derivatives ELI LILLY AND COMPANY (US) 1998-11-24 US disclosed
EP-0460679-B1 Endothelin antagonistic peptide derivatives BANYU PHARMA CO LTD (JP) 1998-10-28 EP disclosed
EP-0617022-B1 6,7, dialkoxy-3,4-dihydroisoquinolin-8-ol, process for preparation thereof and process for preparation of 6,7-dialkoxy-1,2,3,4-tetrahydroisoquinolin-8-ol using the compound BANYU PHARMA CO LTD (JP) 1998-02-11 EP disclosed
US-5691315-A CARDIOVASCULAR DISORDERS; VASODILATOR; BRONCHODILATOR BANYU PHARMACEUTICAL CO., LTD. (JP) 1997-11-25 US disclosed
US-5498717-A CHEMICAL INTERMEDIATES FOR PRODUCING ANTITUMOR POTENTIATORS BANYU PHARMACEUTICAL CO., LTD. (JP) 1996-03-12 US disclosed
US-5470833-A Vasodilators, bronchodilators BANYU PHARMACEUTICAL CO., LTD. (JP) 1995-11-28 US disclosed
US-5446164-A Regioselective cyclization of phenethylamide derivative in presence of phosphoric acid halide, reducing formed compound BANYU PHARMACEUTICAL CO., LTD. (JP) 1995-08-29 US disclosed
US-5444152-A Vasolidator or bronchodilator BANYU PHARMACEUTICAL CO., LTD. (JP) 1995-08-22 US disclosed
EP-0617022-A1 6,7, dialkoxy-3,4-dihydroisoquinolin-8-ol, process for preparation thereof and process for preparation of 6,7-dialkoxy-1,2,3,4-tetrahydroisoquinolin-8-ol using the compound BANYU PHARMACEUTICAL CO., LTD. (JP) 1994-09-28 EP disclosed
EP-0460679-A2 Endothelin antagonistic peptide derivatives Banyu Pharmaceutical Co., Ltd. (JP) 1991-12-11 EP 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-20250034131-A1 DIMETHYL AMINO AZETIDINE AMIDES AS JAK INHIBITORS JAK1, JAK2, JAK3 MAOB 2057/4885BCHE 4048/4885CYP4F2 3294/4885
US-12398135-B2 Dimethyl amino azetidine amides as JAK inhibitors JAK1, JAK2, JAK3 MAOB 2057/4885BCHE 4048/4885CYP4F2 3294/4885
US-12122773-B2 Crystalline hydrate of a JAK inhibitor compound JAK1, JAK2, JAK3 MAOB 4094/4885BCHE 4788/4885CYP4F2 1421/4885
US-20240025897-A1 CRYSTALLINE HYDRATE OF A JAK INHIBITOR COMPOUND JAK1, JAK2, JAK3 MAOB 4094/4885BCHE 4788/4885CYP4F2 1421/4885

“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.