SCHEMBL26685

SCHEMBL26685

Brc1ccc2sc3ccccc3c2c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GPR3 P46089 1/20 0.61
PTPN22 Q9Y2R2 2/20 0.50
EPM2A O95278 1/20 0.50
PTPN2 P17706 1/20 0.50
PTPN1 P18031 1/20 0.50
MAPT P10636 5/20 0.48
ALDH1A1 P00352 4/20 0.48
RAB9A P51151 3/20 0.48
HPGD P15428 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
CYP1A2 P05177 1/20 0.44
KDM4E B2RXH2 3/20 0.43
IDO1 P14902 1/20 0.43
TDO2 P48775 1/20 0.42
MAOA P21397 2/20 0.41
MAOB P27338 2/20 0.41
PTPN7 P35236 1/20 0.41
DUSP3 P51452 1/20 0.41
PTPN12 Q05209 1/20 0.41
TDP1 Q9NUW8 2/20 0.41

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
SCHEMBL29536667 1.00 GPR3 (0.61) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL28283111 0.92 GPR3 (0.52) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL21428331 0.92 GPR3 (0.52) GPR3PTPN22EPM2APTPN2PTPN1
Thiophene SCHEMBL28764714 0.91 GPR3 (0.50) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL19303903 0.89 MAPT (0.49) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL29432245 0.89 EPM2A (0.53) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL216673 0.89 EPM2A (0.53) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL25905297 0.88 MAPT (0.47) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL28338891 0.88 GPR3 (0.47) GPR3PTPN22EPM2APTPN2PTPN1
SCHEMBL29887048 0.87 GPR3 (0.61) GPR3PTPN22EPM2APTPN2PTPN1

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 1315 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119331001-B Efficient narrow-band luminescent material embedded with dibenzothiophene, and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2025-06-10 CN claimed
CN-119331001-A Efficient narrow-band luminescent material embedded with dibenzothiophene, and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2025-01-21 CN claimed
CN-116874476-A Organic blue light main body material and preparation method and application thereof 青岛科技大学 2023-10-13 CN claimed
CN-113896612-B Method for selectively preparing o-chlorotoluene 常州新东化工发展有限公司 2023-07-21 CN claimed
CN-110016335-B Pure organic room temperature phosphorescent material with ether bond and preparation method and application thereof 广东工业大学 2022-01-25 CN claimed
CN-113896612-A Method for selectively preparing o-chlorotoluene 常州新东化工发展有限公司 2022-01-07 CN claimed
CN-112457341-A Preparation method of di- (4-dibenzothiophene-2-phenoxy) axially substituted silicon phthalocyanine 福建师范大学 2021-03-09 CN claimed
CN-112047922-A Benzophenone and benzothiophene-based luminescent material and preparation method and application thereof 广东工业大学 2020-12-08 CN claimed
CN-109705087-B Annular oligomer containing dibenzothiophene unit derivative and preparation method and application thereof 华南协同创新研究院 2020-06-05 CN claimed
CN-101712674-A Alkyl substituted-S,S-dioxo-dibenzothiophene monomer, preparation method and polymer thereof UNIV SOUTH CHINA TECH 2010-05-26 CN claimed
EP-4141041-B1 A POLYMER, A COMPOSITION, AND AN ELECTROLUMINESCENCE DEVICE SAMSUNG ELECTRONICS CO LTD (KR) 2026-04-22 EP disclosed
EP-4063466-B1 ORGANIC OPTOELECTRONIC DEVICE, AND DISPLAY DEVICE INCLUDING SAME SAMSUNG SDI CO LTD (KR) 2026-04-01 EP disclosed
US-12538704-B2 4H-imidazo[1,2-a]imidazoles for electronic applications UDC IRELAND LIMITED (IE) 2026-01-27 US disclosed
US-20250393469-A1 ORGANIC ELECTROLUMINESCENCE DEVICE AND POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE SAMSUNG DISPLAY CO LTD (KR) 2025-12-25 US disclosed
US-12507590-B2 Organic electric element comprising organic compound and electronic device thereof DUK SAN NEOLUX CO., LTD. (KR) 2025-12-23 US disclosed
EP-0405774-A1 2-(substituted-dibenzofuranyl and dibenzothienyl)carbapenem antibacterial agents MERCK & CO. INC. (US) 1991-01-02 EP disclosed
EP-0399293-A1 Process for preparing 2-chloro-4-nitro-alkylbenzene BAYER AG (DE) 1990-11-28 EP disclosed
US-4285961-A MICROBIOCIDES MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1981-08-25 US disclosed
US-4018780-A ANTIALLERGENS RIKER LABORATORIES, INC. (US) 1977-04-19 US disclosed
US-3953601-A Dibenzothiophene derivatives as serum lipid lowering agents AKTIEBOLAGET ASTRA (SW) 1976-04-27 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 (2 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-12538704-B2 4H-imidazo[1,2-a]imidazoles for electronic applications RIF1, NR2E1, NR3C1 GPR3 1454/4885PTPN22 1029/4885EPM2A 1391/4885
US-20250393469-A1 ORGANIC ELECTROLUMINESCENCE DEVICE AND POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE SOD1, LIFR, LEF1 GPR3 4172/4885PTPN22 1058/4885EPM2A 643/4885

“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.