SCHEMBL7743398

SCHEMBL7743398

CCC(N)[Si](C)(C)c1ccccc1

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOA P21397 4/20 0.35
SLC6A2 P23975 2/20 0.35
TAAR1 Q96RJ0 2/20 0.35
SLC6A4 P31645 1/20 0.35
SLC6A3 Q01959 1/20 0.35
SIGMAR1 Q99720 1/20 0.35
LMNA P02545 1/20 0.35
CYP2A6 P11509 1/20 0.35
ADORA2A P29274 1/20 0.35
ADORA1 P30542 1/20 0.35
ESR1 P03372 1/20 0.34
ESR2 Q92731 1/20 0.34
ANPEP P15144 1/20 0.34
LAP3 P28838 1/20 0.34
CYP2D6 P10635 1/20 0.33
EPHX1 P07099 1/20 0.33
NR1H2 P55055 1/20 0.32
NR1H3 Q13133 1/20 0.32
MAOB P27338 1/20 0.32
DPP4 P27487 2/20 0.32

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
SCHEMBL8339719 0.89 NR1H2 (0.38) SLC6A4ESR1NR1H2NR1H3
SCHEMBL28591973 0.83 TAAR1 (0.40) MAOASLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL14977000 0.82 CSNK1E (0.33)
SCHEMBL16177937 0.80 CSNK1E (0.38)
SCHEMBL6003566 0.80 SLC6A2 (0.32) MAOASLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL27550597 0.80 MAOA (0.37) MAOASLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL2244551 0.78 SLC6A2 (0.32) MAOASLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL14976317 0.77 CSNK1E (0.46)
SCHEMBL2832122 0.76 SLC6A2 (0.31) MAOASLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL2012876 0.75 SLC6A2 (0.39) MAOASLC6A2TAAR1SLC6A4SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2782920-B1 FUNGICIDE N-[(TRISUBSTITUTEDSILYL)METHYL]-CARBOXAMIDE DERIVATIVES BAYER IP GMBH (DE) 2016-12-21 EP claimed
US-20140315858-A1 FUNGICIDE N-[(TRISUBSTITUTEDSILYL)METHYL]-CARBOXAMIDE DERIVATIVES BAYER INTELLECTUAL PROPERTY GMBH (DE) 2014-10-23 US claimed
CN-102351174-A Preparation method of dispersible silane functionalized graphene UNIV SOUTH CHINA TECH 2012-02-15 CN claimed
EP-0929841-A4 METHOD FOR FORMING PHOTORESIST FEATURES HAVING REENTRANT PROFILES USING A BASIC AGENT MKE QUANTUM COMPONENTS COLORAD (US) 2001-04-18 EP claimed
US-5955244-A Method for forming photoresist features having reentrant profiles using a basic agent QUANTUM CORPORATION (US) 1999-09-21 US claimed
EP-0929841-A1 METHOD FOR FORMING PHOTORESIST FEATURES HAVING REENTRANT PROFILES USING A BASIC AGENT Mke-Quantum Components Colorado LLC (US) 1999-07-21 EP claimed
WO-1998008143-A1 METHOD FOR FORMING PHOTORESIST FEATURES HAVING REENTRANT PROFILES USING A BASIC AGENT MKE-QUANTUM COMPONENTS COLORADO LLC (US) 1998-02-26 WO claimed
US-9617286-B2 Fungicide N-[(trisubstitutedsilyl)methyl]-carboxamide derivatives BAYER INTELLECTUAL PROPERTY GMBH (DE) 2017-04-11 US disclosed
EP-2782920-B1 FUNGICIDE N-[(TRISUBSTITUTEDSILYL)METHYL]-CARBOXAMIDE DERIVATIVES BAYER IP GMBH (DE) 2016-12-21 EP disclosed
US-20140315858-A1 FUNGICIDE N-[(TRISUBSTITUTEDSILYL)METHYL]-CARBOXAMIDE DERIVATIVES BAYER INTELLECTUAL PROPERTY GMBH (DE) 2014-10-23 US disclosed
CN-102351174-A Preparation method of dispersible silane functionalized graphene UNIV SOUTH CHINA TECH 2012-02-15 CN disclosed
EP-0929841-A4 METHOD FOR FORMING PHOTORESIST FEATURES HAVING REENTRANT PROFILES USING A BASIC AGENT MKE QUANTUM COMPONENTS COLORAD (US) 2001-04-18 EP disclosed
US-5955244-A Method for forming photoresist features having reentrant profiles using a basic agent QUANTUM CORPORATION (US) 1999-09-21 US disclosed
US-4822830-A CROSSLINKED WITH AMINOORGANOSILICON COMPOUND AND ALUMINA TRIHYDRATE; MOISTURE CURED WACKER SILICONES CORPORATION (US) 1989-04-18 US disclosed
EP-0017734-B1 CURABLE ORGANOPOLYSILOXANE COMPOSITIONS CONTAINING CARBON BLACK, METHOD FOR PREPARING THE SAME AND METHOD FOR CURING THE COMPOSITIONS SWS Silicones Corporation (US) 1983-04-13 EP disclosed
US-4301056-A OBTAINED BY CROSSLINKING A POLYSILOXANE, ORGANIC PEROXIDE, AND A HYDROPHOBIC CALCIUM HYDROXIDE WACKER-CHEMIE GMBH (DE) 1981-11-17 US disclosed
EP-0017734-A1 Curable organopolysiloxane compositions containing carbon black, method for preparing the same and method for curing the compositions SWS Silicones Corporation (US) 1980-10-29 EP disclosed
US-4221693-A ROOM TEMPERATURE VULCANIZED SILICONE RUBBERS WACKER SILICONES CORPORATION 1980-09-09 US disclosed
US-4184880-A RELEASE AGENTS WACKER-CHEMIE GMBH (DE) 1980-01-22 US disclosed
US-4111890-A CURABLE ORGANOPOLYSILOXANE COMPOSITIONS CONTAINING TITANIUM ESTERS SWS SILICONES CORPORATION (US) 1978-09-05 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-20140315858-A1 FUNGICIDE N-[(TRISUBSTITUTEDSILYL)METHYL]-CARBOXAMIDE DERIVATIVES TET3, TET1, PFAS MAOA 1898/4885SLC6A2 3457/4885TAAR1 3044/4885

“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.