SCHEMBL3215328

SCHEMBL3215328

N#Cc1ccc(C(=O)c2ccccc2)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.61
SRD5A2 P31213 1/20 0.58
CA1 P00915 2/20 0.57
CA2 P00918 2/20 0.57
LMNA P02545 3/20 0.56
L3MBTL1 Q9Y468 2/20 0.56
MAPT P10636 2/20 0.56
TSHR P16473 1/20 0.54
KMT2A Q03164 3/20 0.53
ATM Q13315 2/20 0.53
KDM4E B2RXH2 1/20 0.53
PKM P14618 1/20 0.53
TDP1 Q9NUW8 1/20 0.52
GSK3B P49841 2/20 0.52
MEN1 O00255 2/20 0.50
RAB9A P51151 2/20 0.50
NPC1 O15118 2/20 0.50
HPGD P15428 2/20 0.50
PGR P06401 1/20 0.50
MAPK13 O15264 1/20 0.50

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
SCHEMBL13063665 0.94 MAPT (0.60) ALDH1A1SRD5A2CA1CA2LMNA
SCHEMBL9967905 0.94 MAPT (0.60) ALDH1A1SRD5A2CA1CA2LMNA
SCHEMBL13445156 0.94 MAPT (0.60) ALDH1A1SRD5A2CA1CA2LMNA
SCHEMBL13063666 0.94 MAPT (0.60) ALDH1A1SRD5A2CA1CA2LMNA
Benzophenone SCHEMBL9307169 0.93 ALDH1A1 (0.64) ALDH1A1SRD5A2CA1CA2LMNA
SCHEMBL3433075 0.91 CA2 (0.67) ALDH1A1SRD5A2CA1CA2LMNA
SCHEMBL6413833 0.87 CES2 (0.65) ALDH1A1CA1CA2LMNAL3MBTL1
SCHEMBL7101031 0.85 MAOA (0.72) ALDH1A1SRD5A2CA1CA2LMNA
Benzophenone SCHEMBL8986537 0.84 KMT2A (0.68) ALDH1A1SRD5A2LMNAL3MBTL1MAPT
Isonicotinonitrile SCHEMBL9710828 0.83 KMT2A (0.71) ALDH1A1SRD5A2LMNAL3MBTL1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118772077-A Tetraphenyl ethylene biological orthogonal activation type photosensitizer and preparation method and application thereof 中国医学科学院药物研究所 2024-10-15 CN claimed
CN-114057790-A Preparation method of vitamin A triphenylphosphine salt with high all-trans isomer content 万华化学集团股份有限公司 2022-02-18 CN claimed
EP-3143055-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP Bridgestone Corporation (JP) 2017-03-22 EP claimed
WO-2015175280-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP BRIDGESTONE CORPORATION (JP) 2015-11-19 WO claimed
EP-0043480-B1 PROCESS FOR FORMING METALLIC IMAGES Hitachi, Ltd. (JP) 1985-04-03 EP claimed
US-4347304-A PHOTOSENSITIZATION WITH DISILANES OR ORGANIC COMPOUNDS HAVING COUPLED GERMANIUM OR TIN MOLECULES; PHOTORESISTS; POSITIVES; PLATING HITACHI, LTD. (JP) 1982-08-31 US claimed
EP-0043480-A2 Process for forming metallic images Hitachi, Ltd. (JP) 1982-01-13 EP claimed
US-12540247-B2 Primer composition THREEBOND CO., LTD. (JP) 2026-02-03 US disclosed
CN-119376184-A Composition comprising a surface treatment component or a cure promoting component 三键有限公司 2025-01-28 CN disclosed
EP-3981754-B1 METHOD FOR MANUFACTURING 1-HALO-2-FLUOROETHYLENE DAIKIN IND LTD (JP) 2024-11-06 EP disclosed
CN-118851893-A New synthetic method of diaryl ketone derivative 河南大学 2024-10-29 CN disclosed
CN-118772077-A Tetraphenyl ethylene biological orthogonal activation type photosensitizer and preparation method and application thereof 中国医学科学院药物研究所 2024-10-15 CN disclosed
CN-118637970-A Method for producing thioester derivative, method for producing ketone derivative, and method for producing aldehyde derivative 株式会社德山 2024-09-13 CN disclosed
US-4070499-A Method for crosslinking ultraviolet light curable coatings PPG INDUSTRIES, INC. (US) 1978-01-24 US disclosed
US-4052283-A FROM ALLENE AND HYDROGEN SULFIDE, POLYMERIZATION HOOKER CHEMICALS & PLASTICS CORPORATION (US) 1977-10-04 US disclosed
US-4046577-A PHOTOREACTIVE COMPOSITIONS COMPRISING POLYMERS CONTAINING ALKOXYAROMATIC GLYOXY GROUPS THE RICHARDSON COMPANY (US) 1977-09-06 US disclosed
US-4037112-A Apparatus for crosslinking ultraviolet light curable coatings PPG INDUSTRIES, INC. (US) 1977-07-19 US disclosed
US-4024296-A Photocatalyst system and pigmented actinic light polymerizable coating compositions containing the same PPG INDUSTRIES, INC. (US) 1977-05-17 US disclosed
US-4017652-A Photocatalyst system and ultraviolet light curable coating compositions containing the same PPG INDUSTRIES, INC. (US) 1977-04-12 US disclosed
US-3992274-A ALLENE COMPOUNDS, HYDROGEN SULFIDE, PHOTOSENSITIZING AGENT HOOKER CHEMICALS & PLASTICS CORPORATION (US) 1976-11-16 US 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-12540247-B2 Primer composition FGB, CDH1, F10 ALDH1A1 1171/4885SRD5A2 1746/4885CA1 4204/4885

“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.