SCHEMBL53374

SCHEMBL53374

CC(C)(O[SiH3])C(c1ccccc1)c1ccccc1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 4/20 0.37
RIPK1 Q13546 2/20 0.36
SLC6A4 P31645 2/20 0.36
SLC6A3 Q01959 2/20 0.36
SLC6A2 P23975 1/20 0.36
HTR2A P28223 1/20 0.36
ATM Q13315 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
MAPK1 P28482 1/20 0.34
AOC3 Q16853 1/20 0.34
CACNA1F O60840 1/20 0.34
CHRM2 P08172 1/20 0.34
CHRM1 P11229 1/20 0.34
ADRA2B P18089 1/20 0.34
CHRM3 P20309 1/20 0.34
ADRA1A P35348 1/20 0.34
HRH1 P35367 1/20 0.34
OPRK1 P41145 1/20 0.34
CACNA1D Q01668 1/20 0.34
KCNH2 Q12809 1/20 0.34

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
SCHEMBL6388790 0.81 TAAR1 (0.39) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL704259 0.80 SLC6A4 (0.41) TAAR1RIPK1SLC6A4SLC6A3ATM
SCHEMBL704632 0.78 ATM (0.37) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL3526378 0.77 F2 (0.39) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL3951516 0.77 TAAR1 (0.37) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL705569 0.77 RIPK1 (0.37) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL11770112 0.76 TAAR1 (0.40) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL706206 0.75 LMNA (0.41) RIPK1SLC6A4SLC6A3SLC6A2AOC3
SCHEMBL7074781 0.74 TAAR1 (0.39) TAAR1RIPK1SLC6A4SLC6A3SLC6A2
SCHEMBL707571 0.74 RIPK1 (0.35) TAAR1RIPK1SLC6A4SLC6A3SLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116375779-A Method for stereoselective synthesis of 2' -deoxyribonucleoside 中国药科大学 2023-07-04 CN claimed
US-10662202-B2 Synthesis of cephalosporin compounds MERCK SHARP & DOHM CORP. (US) 2020-05-26 US claimed
US-10632099-B2 Non-aromatic difluoro analogues of resorcylic acid lactones UNIVERSITY OF NORTH CAROLINA AT GREENSBORO (US) 2020-04-28 US claimed
US-20180153854-A1 NON-AROMATIC DIFLUORO ANALOGUES OF RESORCYLIC ACID LACTONES NORTH CAROLINA AT GREENSBORO, UNIVERSITY OF 2018-06-07 US claimed
EP-2308861-B1 MACROCYCLIC COMPOUNDS USEFUL AS PHARMACEUTICALS EISAI R&D MAN CO LTD (JP) 2017-03-01 EP claimed
EP-1910387-B1 COMPOUNDS FOR PREPARING IMMUNOLOGICAL ADJUVANT EISAI R&D MAN CO LTD (JP) 2016-11-16 EP claimed
EP-2427057-B1 BENZOFURAN-4,5-DIONES AS SELECTIVE PEPTIDE DEFORMYLASE INHIBITORS SLOAN KETTERING INST CANCER (US) 2015-08-12 EP claimed
US-20130217900-A1 CHIRAL INTERMEDIATES USEFUL FOR THE PREPARATION OF HYDROXYPHOSPHINE LIGANDS UNITED PHOSPHORUS LIMITED (IN) 2013-08-22 US claimed
US-7915306-B2 For therapy of inflammatory or autoimmune disorders EISAI CO., LTD. (JP) 2011-03-29 US claimed
US-7683200-B2 Compounds for preparing immunological adjuvant EISAI R & D MANAGEMENT CO., LTD. (JP) 2010-03-23 US claimed
US-11986481-B2 Method of synthesizing thyroid hormone analogs and polymorphs thereof MADRIGAL PHARMACEUTICALS, INC. (US) 2024-05-21 US disclosed
US-20240148742-A1 METHOD OF SYNTHESIZING THYROID HORMONE ANALOGS AND POLYMORPHS THEREOF MADRIGAL PHARMACEUTICALS, INC. 2024-05-09 US disclosed
EP-4023641-B1 METHOD OF SYNTHESIZING THYROID HORMONE ANALOGS AND POLYMORPHS THEREOF MADRIGAL PHARMACEUTICALS INC (US) 2024-05-01 EP disclosed
US-11964025-B2 Peptide-containing linkers for antibody-drug conjugates MERSANA THERAPEUTICS, INC. (US) 2024-04-23 US disclosed
US-20240122936-A1 METHOD OF SYNTHESIZING THYROID HORMONE ANALOGS AND POLYMORPHS THEREOF LSI FINANCING LLC, AS ADMINISTRATIVE AGENT 2024-04-18 US disclosed
US-4681962-A BLOOD PLATELET ANTI-AGGREGATING AGENTS HOFFMANN-LA ROCHE INC. (US) 1987-07-21 US disclosed
US-4680419-A ANTHELMINTICS THE UPJOHN COMPANY (US) 1987-07-14 US disclosed
US-4680415-A ANTICOAGULANTS HOFFMANN-LA ROCHE INC. (US) 1987-07-14 US disclosed
EP-0209694-A1 Novel prostacyclins F. HOFFMANN-LA ROCHE AG (CH) 1987-01-28 EP disclosed
US-4634782-A PROSTAGLANDINS, ANTICOAGULANTS, HYPOTENSIVES HOFFMANN-LA ROCHE INC. (US) 1987-01-06 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 (8 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-10662202-B2 Synthesis of cephalosporin compounds COASY, DDT, PEPD TAAR1 4511/4885RIPK1 3011/4885SLC6A4 3836/4885
US-11986481-B2 Method of synthesizing thyroid hormone analogs and polymorphs thereof THRB, TSHR, TRHR TAAR1 1396/4885RIPK1 3507/4885SLC6A4 1583/4885
US-20240122936-A1 METHOD OF SYNTHESIZING THYROID HORMONE ANALOGS AND POLYMORPHS THEREOF THRB, TSHR, TRHR TAAR1 1396/4885RIPK1 3507/4885SLC6A4 1583/4885
US-20130217900-A1 CHIRAL INTERMEDIATES USEFUL FOR THE PREPARATION OF HYDROXYPHOSPHINE LIGANDS CYP21A2, HRH3, P4HA1 TAAR1 501/4885RIPK1 4058/4885SLC6A4 811/4885
US-20240148742-A1 METHOD OF SYNTHESIZING THYROID HORMONE ANALOGS AND POLYMORPHS THEREOF THRB, TSHR, TRHR TAAR1 1396/4885RIPK1 3507/4885SLC6A4 1583/4885
US-20180153854-A1 NON-AROMATIC DIFLUORO ANALOGUES OF RESORCYLIC ACID LACTONES FRS2, FGFR3, FDPS TAAR1 4461/4885RIPK1 1664/4885SLC6A4 3603/4885
US-11964025-B2 Peptide-containing linkers for antibody-drug conjugates CD2BP2, DNPEP, LNPEP TAAR1 4062/4885RIPK1 2630/4885SLC6A4 3603/4885
US-10632099-B2 Non-aromatic difluoro analogues of resorcylic acid lactones FRS2, FGFR3, FDPS TAAR1 4461/4885RIPK1 1664/4885SLC6A4 3603/4885

“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.