SCHEMBL5887704

SCHEMBL5887704

c1ccc(-c2cccc3c4ccccc4c4ccccc4c23)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.46
HSD17B10 Q99714 4/20 0.46
HPGD P15428 4/20 0.46
CYP1A2 P05177 1/20 0.46
THRB P10828 1/20 0.46
LIMK1 P53667 2/20 0.45
CLK4 Q9HAZ1 2/20 0.45
PLK4 O00444 1/20 0.45
MAPK9 P45984 1/20 0.45
AKT3 Q9Y243 1/20 0.45
MAPK1 P28482 2/20 0.44
BCL2L1 Q07817 1/20 0.44
CYP2A6 P11509 1/20 0.44
MAP4K4 O95819 1/20 0.44
CSF1R P07333 1/20 0.44
FGFR1 P11362 1/20 0.44
PDGFRA P16234 1/20 0.44
LTK P29376 1/20 0.44
KDR P35968 1/20 0.44
MAPK8 P45983 1/20 0.44

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
Benzene SCHEMBL29177892 1.00 ALDH1A1 (0.46) ALDH1A1HSD17B10HPGDCYP1A2THRB
Biphenyl SCHEMBL29177817 0.97 ALDH1A1 (0.45) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL25421508 0.95 ALDH1A1 (0.43) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL26087273 0.92 ALDH1A1 (0.48) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL30303049 0.90 ALDH1A1 (0.48) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL30302742 0.90 ALDH1A1 (0.48) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL30021443 0.90 ALDH1A1 (0.48) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL2591950 0.90 ALDH1A1 (0.48) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL22717357 0.90 LIMK1 (0.42) ALDH1A1HSD17B10HPGDCYP1A2THRB
SCHEMBL30302621 0.90 ALDH1A1 (0.46) ALDH1A1HSD17B10HPGDCYP1A2THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108063188-B Organic light emitting element 株式会社LG化学 2020-08-11 CN claimed
CN-108063188-A Organic light emitting element 株式会社LG化学 2018-05-22 CN claimed
CN-108046976-A A kind of preparation method of trisubstituted benzene 赵东敏 2018-05-18 CN claimed
EP-0428708-B1 PROCESS FOR PREPARING A POLYMER HAVING PERFLUOROCYCLOBUTANE RINGS AND POLYMERS CONTAINING PERFLUOROCYCLOBUTANE RINGS DOW CHEMICAL CO (US) 1994-10-05 EP claimed
EP-0428706-B1 PERFLUOROVINYL COMPOUNDS DOW CHEMICAL CO (US) 1994-07-13 EP claimed
US-12559673-B2 Organic electroluminescent element NIPPON STEEL CHEMICAL & MATERIAL CO., LTD. (JP) 2026-02-24 US disclosed
CN-114521299-B Organic electroluminescent element and method for manufacturing the same 日铁化学材料株式会社 2025-05-13 CN disclosed
CN-113710770-B Organic electroluminescent element and method for manufacturing the same 日铁化学材料株式会社 2024-12-31 CN disclosed
CN-118339941-A Mixed powder and method for producing same, method for producing organic electroluminescent element using same, method for selecting compound in mixed powder, and composition for vacuum vapor deposition 出光兴产株式会社 2024-07-12 CN disclosed
US-20240213072-A1 LAMINATE, RELEASE AGENT COMPOSITION, AND METHOD FOR MANUFACTURING PROCESSED SEMICONDUCTOR SUBSTRATE NISSAN CHEMICAL CORPORATION (JP) 2024-06-27 US disclosed
US-20240208179-A1 LAMINATE, RELEASE AGENT COMPOSITION, AND METHOD FOR MANUFACTURING PROCESSED SEMICONDUCTOR SUBSTRATE NISSAN CHEMICAL CORPORATION (JP) 2024-06-27 US disclosed
US-20240199924-A1 LAMINATE, RELEASE AGENT COMPOSITION, AND METHOD FOR MANUFACTURING PROCESSED SEMICONDUCTOR SUBSTRATE NISSAN CHEMICAL CORPORATION (JP) 2024-06-20 US disclosed
US-5409777-A Protective coatings THE DOW CHEMICAL COMPANY (US) 1995-04-25 US disclosed
EP-0428708-B1 PROCESS FOR PREPARING A POLYMER HAVING PERFLUOROCYCLOBUTANE RINGS AND POLYMERS CONTAINING PERFLUOROCYCLOBUTANE RINGS DOW CHEMICAL CO (US) 1994-10-05 EP disclosed
EP-0428706-B1 PERFLUOROVINYL COMPOUNDS DOW CHEMICAL CO (US) 1994-07-13 EP disclosed
US-5246782-A Electronic devices THE DOW CHEMICAL COMPANY (US) 1993-09-21 US disclosed
CN-1073137-A The laminating material and the polymkeric substance that contains perfluoro cyclobutane ring that contain the perfluorocyclobutane cyclopolymer DOW CHEMICAL CO (US) 1993-06-16 CN disclosed
EP-0490335-A2 Laminates of polymers having perfluorocyclobutane rings and polymers containing perfluorocyclobutane rings THE DOW CHEMICAL COMPANY (US) 1992-06-17 EP disclosed
EP-0428706-A1 PERFLUOROVINYL COMPOUNDS. DOW CHEMICAL CO (US) 1991-05-29 EP disclosed
WO-1990015043-A2 PERFLUOROVINYL COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1990-12-13 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 (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-12559673-B2 Organic electroluminescent element CACNA1S, CACNA2D1, LBR ALDH1A1 1103/4885HSD17B10 3791/4885HPGD 4556/4885

“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.