SCHEMBL64121

SCHEMBL64121

[CH2]C(=O)c1ccc2ccccc2c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 1/20 0.68
CES1 P23141 1/20 0.68
SMN1; SMN2 Q16637 3/20 0.62
KDM4E B2RXH2 2/20 0.62
HPGD P15428 2/20 0.62
ALDH1A1 P00352 2/20 0.62
MEN1 O00255 1/20 0.62
EGFR P00533 1/20 0.62
TP53 P04637 1/20 0.62
CYP3A4 P08684 1/20 0.62
MAPT P10636 1/20 0.62
PKM P14618 1/20 0.62
ALOX15 P16050 1/20 0.62
ALOX12 P18054 1/20 0.62
JAK1 P23458 1/20 0.62
MAPK1 P28482 1/20 0.62
KMT2A Q03164 1/20 0.62
HSD17B10 Q99714 1/20 0.62
TDP1 Q9NUW8 1/20 0.62
PTPN1 P18031 1/20 0.57

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
SCHEMBL29462782 0.82 CES2 (0.68) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL546633 0.82 CES2 (0.68) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL26903783 0.82 CES2 (0.68) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL7220072 0.81 CES2 (1.00) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL30250451 0.81 CES2 (0.74) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL941698 0.81 CES2 (0.74) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL31032483 0.81 CES2 (1.00) CES2CES1SMN1; SMN2KDM4EHPGD
SCHEMBL29613672 0.81 CES2 (0.74) CES2CES1SMN1; SMN2KDM4EHPGD
Hydrochloric Acid SCHEMBL8358165 0.80 CES2 (0.65) CES2CES1SMN1; SMN2KDM4EHPGD
Hydrochloric Acid SCHEMBL22558829 0.80 CES2 (0.65) CES2CES1SMN1; SMN2KDM4EHPGD

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 1258 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110078717-B Bis-benzofuran-benzimidazole salt compound with anti-tumor activity and preparation method thereof 红河学院 2022-04-26 CN claimed
CN-109053847-B 17 β -imidazolidinyl bromide-dehydroepiandrostane derivative and preparation method and application thereof 云南大学 2020-05-19 CN claimed
CN-106916144-B N-alkyl substituted indole-imidazole salt compound and preparation method thereof 云南民族大学 2020-05-05 CN claimed
CN-106543147-A A kind of substituted carbazole-imidazole salts or benzimidazole salt compound and preparation method thereof 云南大学 2017-03-29 CN claimed
CN-106478653-A Isosorbide imidazole salt compound and preparation method thereof 云南民族大学 2017-03-08 CN claimed
CN-102617445-B Photosensitive compositions, curable compositions, novel compounds, photopolymerizable compositions, color filters, and planographic printing plate precursors FUJIFILM CORP 2015-02-18 CN claimed
US-20070049594-A1 Novel compounds and compositions as cathepsin inhibitors AVENTIS PHARMACEUTICALS INC. (US) 2007-03-01 US claimed
EP-1383748-A2 NOVEL COMPOUNDS AND COMPOSITIONS AS CATHEPSIN INHIBITORS AXYS PHARMACEUTICALS, INC. (US) 2004-01-28 EP claimed
WO-2002051983-A2 NOVEL COMPOUNDS AND COMPOSITIONS AS CATHEPSIN INHIBITORS AXYS PHARMACEUTICALS, INC. (US) 2002-07-04 WO claimed
US-20240241442-A1 Positive Resist Material And Patterning Process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2024-07-18 US disclosed
US-12013639-B2 Positive resist material and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2024-06-18 US disclosed
US-20240192591-A1 RESIST COMPOSITION AND PATTERN FORMING PROCESS SHIN-ETSU CHEMICAL CO., LTD. (JP) 2024-06-13 US disclosed
CN-114660896-B Composition for forming silicon-containing resist underlayer film, pattern forming method, and silicon compound 信越化学工业株式会社 2024-06-11 CN disclosed
US-12001138-B2 Composition for forming silicon-containing resist underlayer film and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2024-06-04 US disclosed
EP-0232776-A2 2,5,6,7-tetranor-4,8-inter-m-phenylene PGI2 derivatives TORAY INDUSTRIES, INC. (JP) 1987-08-19 EP disclosed
US-4564620-A 5,6,7,-Trinor-4,8-inter-m-phenylene PGI2 derivatives and anti-ulcer, anti-thrombotic and anti-hypertensive pharmaceutical compositions containing them TORAY INDUSTRIES, INC. (JP) 1986-01-14 US disclosed
EP-0024943-B1 5,6,7-TRINOR-4,8-INTER-M-PHENYLENE PGI2 DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM TORAY INDUSTRIES, INC. (JP) 1983-08-17 EP disclosed
EP-0060640-A1 5,6,7-Trinor-4,8-inter-m-phenylene PGI derivatives and pharmaceutical compositions containing them TORAY INDUSTRIES, INC. (JP) 1982-09-22 EP disclosed
US-4301164-A FOR USE AS ANTIULCER AGENTS, HYPOTENSIVE AGENTS, ANTITHROMBOSIC AGENTS TORAY INDUSTRIES, INC. (JP) 1981-11-17 US disclosed
EP-0024943-A1 5,6,7-Trinor-4,8-inter-m-phenylene PGI2 derivatives and pharmaceutical compositions containing them TORAY INDUSTRIES, INC. (JP) 1981-03-11 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 (1 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-20070049594-A1 Novel compounds and compositions as cathepsin inhibitors CTSS, CTSB, CTSE CES2 351/4885CES1 154/4885SMN1; SMN2 3350/4885

“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.