SCHEMBL1246652

SCHEMBL1246652

O=C(O)c1ccc(N(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.59
DAO P14920 1/20 0.59
NAPRT Q6XQN6 1/20 0.59
TP53 P04637 1/20 0.57
SRD5A2 P31213 2/20 0.56
CES2 O00748 1/20 0.56
CES1 P23141 1/20 0.56
ALDH1A1 P00352 3/20 0.50
L3MBTL1 Q9Y468 2/20 0.50
KDM4E B2RXH2 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2D6 P10635 1/20 0.50
MAPT P10636 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
TRPA1 O75762 1/20 0.50
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48

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
SCHEMBL2596293 1.00 TSHR (0.59) TSHRDAONAPRTTP53SRD5A2
Terephthalic Acid SCHEMBL10615446 0.98 TSHR (0.62) TSHRDAONAPRTTP53SRD5A2
SCHEMBL14769783 0.94 EGFR (0.53) TSHRDAONAPRTTP53SRD5A2
SCHEMBL21760526 0.94 EGFR (0.53) TSHRDAONAPRTTP53SRD5A2
Benzoic Acid SCHEMBL21145080 0.93 TSHR (0.70) TSHRDAONAPRTTP53SRD5A2
SCHEMBL22972761 0.93 TSHR (0.67) TSHRDAONAPRTTP53SRD5A2
SCHEMBL2029621 0.93 TSHR (0.67) TSHRDAONAPRTTP53SRD5A2
SCHEMBL17040204 0.93 TSHR (0.67) TSHRDAONAPRTTP53SRD5A2
SCHEMBL21765823 0.92 EGFR (0.56) TSHRDAONAPRTSRD5A2ALDH1A1
SCHEMBL14856712 0.88 HDAC1 (0.50) TSHRDAONAPRTSRD5A2CES2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122054808-A Surface modification method of perovskite light absorption layer and application of surface modification method in preparation of inverted-structure perovskite solar cell 贵州大学 2026-05-15 CN claimed
CN-117603206-A Mitochondrial fluorescent probe and preparation method and application thereof 云南大学 2024-02-27 CN claimed
CN-114057663-B Triphenylamine derivative with mechanochromatic characteristic and preparation method and application thereof 吉林大学 2023-09-08 CN claimed
CN-114057663-A Triphenylamine derivative with mechanochromic characteristic and preparation method and application thereof 吉林大学 2022-02-18 CN claimed
CN-112010943-B To Cu2+Sensitive organic small molecule gel compound and preparation method and application thereof 温州大学 2022-02-15 CN claimed
CN-112939888-A Star-shaped D-A type conjugated molecule and synthetic method and application thereof 吉林大学 2021-06-11 CN claimed
CN-112010943-A To Cu2+Sensitive organic small molecule gel compound and preparation method and application thereof 温州大学 2020-12-01 CN claimed
CN-111892552-A Triphenylamine derivative, preparation method thereof and application thereof in double-channel fluorescence detection of hydrogen sulfide 山西大学 2020-11-06 CN claimed
JP-11035535-A None JP disclosed
CN-122054808-A Surface modification method of perovskite light absorption layer and application of surface modification method in preparation of inverted-structure perovskite solar cell 贵州大学 2026-05-15 CN disclosed
US-20250074925-A1 RARE EARTH COMPLEX SAGAMI CHEMICAL RESEARCH INSTITUTE (JP) 2025-03-06 US disclosed
CN-108290875-B Compound for organic electronic element, organic electronic element using same, and electronic device using same 德山新勒克斯有限公司 2024-09-17 CN disclosed
EP-4365180-A1 RARE EARTH COMPLEX Tosoh Corporation (JP) 2024-05-08 EP disclosed
CN-117616032-A Rare earth complex 东曹株式会社 2024-02-27 CN disclosed
EP-0011980-B1 PHOTOCONDUCTIVE LAYERS CONTAINING A MIXTURE OF AT LEAST TWO DIFFERENT ORGANIC PHOTOCONDUCTORS AND ELECTROPHOTOGRAPHIC ELEMENTS COMPRISING SAID LAYERS EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1984-03-28 EP disclosed
US-4322487-A Composite electrically photosensitive particles for electrophoretic migration imaging process EASTMAN KODAK COMPANY (US) 1982-03-30 US disclosed
US-4301226-A FOR USE IN ELECTOGRAPHY EASTMAN KODAK COMPANY (US) 1981-11-17 US disclosed
EP-0011980-A1 Photoconductive layers containing a mixture of at least two different organic photoconductors and electrophotographic elements comprising said layers EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1980-06-11 EP disclosed
US-4018606-A Organic azo pigment sensitizers for photoconductive layers EASTMAN KODAK COMPANY (US) 1977-04-19 US disclosed
US-4018607-A Crystalline organic pigment sensitizers for photoconductive layers EASTMAN KODAK COMPANY (US) 1977-04-19 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-20250074925-A1 RARE EARTH COMPLEX L1CAM, CHRM1, NPM1 TSHR 1180/4885DAO 4348/4885NAPRT 3577/4885

“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.