SCHEMBL2804365

SCHEMBL2804365

CCCCCCCCCCCCCCCCCC[Si](C)(C)[O]

nearest known ligand 0.47

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.47
THRB P10828 1/20 0.47
EPHX1 P07099 4/20 0.39
CES2 O00748 3/20 0.38
CES1 P23141 3/20 0.38
EPHX2 P34913 1/20 0.38
DNM1 Q05193 4/20 0.36
ALDH1A1 P00352 2/20 0.36
LMNA P02545 2/20 0.36
HSD17B10 Q99714 1/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36

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
SCHEMBL17090824 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090807 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090815 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090809 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL1494494 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090822 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090765 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL17090838 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL1494268 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1
SCHEMBL1494192 1.00 TSHR (0.47) TSHRTHRBEPHX1CES2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118027672-A 3D (three-dimensional) direct writing printing porous silicon rubber and preparation method thereof 中国科学院化学研究所 2024-05-14 CN disclosed
CN-117986876-A Organic silicon foam and preparation method thereof 中国科学院化学研究所 2024-05-07 CN disclosed
CN-109415447-B Silane-mediated enhancement of rubber storage stability 盛禧奥欧洲有限责任公司 2021-06-15 CN disclosed
CN-106146851-B Photocurable composition and cured product containing same 信越化学工业株式会社 2020-10-23 CN disclosed
US-10787562-B2 Silane-mediated enhancement of rubber storage stability TRINSEO EUROPE GMBH (CH) 2020-09-29 US disclosed
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2020-08-04 US disclosed
EP-2921499-B1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACIDS TAKEDA PHARMACEUTICALS CO (JP) 2020-01-22 EP disclosed
EP-3093303-B1 PHOTOCURABLE COMPOSITION AND CURED PRODUCT SHINETSU CHEMICAL CO (JP) 2019-08-28 EP disclosed
US-20190169406-A1 SILANE-MEDIATED ENHANCEMENT OF RUBBER STORAGE STABILITY TRINSEO EUROPE GMBH (CH) 2019-06-06 US disclosed
US-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2019-05-09 US disclosed
US-5762803-A Silicon dioxide based microspheres for rapid chromatographic separation of biomolecules CU CHEMIE UETIKON AG (CH) 1998-06-09 US disclosed
WO-1998008525-A1 PROCESS TO OBTAIN OESTROGENS FROM MARE'S URINE SOLVAY DEUTSCHLAND GMBH (DE) 1998-03-05 WO disclosed
EP-0693314-A1 Silicon dioxide based adsorbents for chromatography CU CHEMIE UETIKON AG (CH) 1996-01-24 EP disclosed
EP-0344891-B1 Tetraazaporphin, process for producing the same, as well as optical recording media using the same and production processes thereof HITACHI CHEMICAL CO LTD (JP) 1994-07-27 EP disclosed
US-5284943-A Containing Si, Ge or Sn HITACHI CHEMICAL COMPANY, CO. (JP) 1994-02-08 US disclosed
US-5217856-A TETRAAZAPORPHIN, PROCESS FOR PRODUCING THE SAME, AS WELL AS OPTICAL RECORDING MEDIA USING THE SAME AND PRODUCTION PROCESSES THEREOF HITACHI CHEMICAL CO., LTD. (JP) 1993-06-08 US disclosed
EP-0344891-A2 Tetraazaporphin, process for producing the same, as well as optical recording media using the same and production processes thereof Hitachi Chemical Co., Ltd. (JP) 1989-12-06 EP disclosed
EP-0101597-B1 PROCESS FOR THE PREPARATION OF ASTAXANTHINE AND INTERMEDIATES IN THE ASTAXANTHINE SYNTHESIS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1988-06-22 EP disclosed
US-4585885-A INTERMEDIATES FOR ASTAXANTHIN HOFFMANN-LA ROCHE INC. (US) 1986-04-29 US disclosed
EP-0101597-A2 Process for the preparation of astaxanthine and intermediates in the astaxanthine synthesis F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-02-29 EP 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-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID RNGTT, POLR2H, POLR2E TSHR 551/4885THRB 1506/4885EPHX1 2751/4885
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid RNGTT, POLR2H, POLR2E TSHR 411/4885THRB 1249/4885EPHX1 2124/4885

“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.