SCHEMBL538032

SCHEMBL538032

CO[Si](CN1CCNCC1)(OC)OC

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.35
CHRM2 P08172 1/20 0.35
SLC6A4 P31645 1/20 0.35
OPRD1 P41143 1/20 0.35
OPRK1 P41145 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.34
POLB P06746 1/20 0.34
APOBEC3A P31941 1/20 0.34
CTDSP1 Q9GZU7 1/20 0.34
APOBEC3G Q9HC16 1/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
CXCR4 P61073 2/20 0.33
SIGMAR1 Q99720 2/20 0.32
CHRM5 P08912 1/20 0.32
CHRM3 P20309 1/20 0.32
LMNA P02545 1/20 0.32
PDE4A P27815 1/20 0.31
PDE4B Q07343 1/20 0.31
PDE4C Q08493 1/20 0.31

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
SCHEMBL538013 0.80 CYP1A2 (0.34) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL4066940 0.80 CYP1A2 (0.34) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL557566 0.78 SIGMAR1 (0.33) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL4058397 0.78 MEN1 (0.42) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL2502895 0.78 CARM1 (0.32) LMNA
SCHEMBL1519033 0.77 CYP1A2 (0.33) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL1230677 0.76 HRH3 (0.35) MEN1KMT2ACHRM5LMNA
SCHEMBL329641 0.76 HRH3 (0.35) MEN1KMT2ACHRM5LMNA
SCHEMBL465021 0.75 CXCR4 (0.46) CYP1A2CHRM2SLC6A4OPRD1OPRK1
SCHEMBL1229552 0.74 CSNK2A2 (0.35) MEN1KMT2ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115304641-A Synthesis method of phosphorus-nitrogen synergistic catalyst containing micromolecular silane coupling agent 青岛青颜悦色化工科技有限公司 2022-11-08 CN claimed
US-7569691-B2 Protected piperazino group-bearing organoxysilane compound and making method SHIN-ETSU CHEMICAL CO., LTD. (JP) 2009-08-04 US claimed
CN-116355222-B Washable amino and polyether co-modified polysiloxane and preparation method thereof 山东东岳有机硅材料股份有限公司 2025-05-13 CN disclosed
CN-115947750-A Carboxylated silane coupling agent and preparation method thereof 山东东岳有机硅材料股份有限公司 2023-04-11 CN disclosed
CN-115304641-A Synthesis method of phosphorus-nitrogen synergistic catalyst containing micromolecular silane coupling agent 青岛青颜悦色化工科技有限公司 2022-11-08 CN disclosed
CN-115304641-A Synthesis method of phosphorus-nitrogen synergistic catalyst containing micromolecular silane coupling agent 青岛青颜悦色化工科技有限公司 2022-11-08 CN disclosed
US-10208206-B2 Curable resin composition and cured product thereof, sealing material for optical semiconductor, die bonding material, and optical semiconductor light-emitting element ASAHI KASEI CHEMICALS CORPORATION (JP) 2019-02-19 US disclosed
US-20160115318-A1 Curable Resin Composition and Cured Product Thereof, Sealing Material for Optical Semiconductor, Die Bonding Material, and Optical Semiconductor Light-Emitting Element ASAHI KASEI CHEMICALS CORPORATION (JP) 2016-04-28 US disclosed
EP-2995634-A1 CURABLE RESIN COMPOSITION AND CURED PRODUCT THEREOF, SEALING MATERIAL FOR OPTICAL SEMICONDUCTOR, DIE BONDING MATERIAL, AND OPTICAL SEMICONDUCTOR LIGHT-EMITTING ELEMENT Asahi Kasei Chemicals Corporation (JP) 2016-03-16 EP disclosed
CN-105189599-A Curable resin composition and cured product thereof, sealing material for optical semiconductor, die bonding material, and optical semiconductor light-emitting element ASAHI KASEI CHEMICALS CORP 2015-12-23 CN disclosed
US-9074032-B2 Membranes based on polyvinyl alcohol WACKER CHEMIE AG (DE) 2015-07-07 US disclosed
EP-1831301-A1 REACTIVE SILICIC ACID SUSPENSIONS Wacker Chemie AG (DE) 2007-09-12 EP disclosed
EP-1824904-A1 ALKOXYSILANE-TERMINATED PREPOLYMERS Wacker Chemie AG (DE) 2007-08-29 EP disclosed
EP-1824865-A2 HIGHLY REACTIVE ALPHA-AMINOMETHYL-ALKOXYSILANES HAVING IMPROVED STABILITY Wacker Chemie AG (DE) 2007-08-29 EP disclosed
WO-2007012547-A2 STABILISED HDK SUSPENSIONS FOR REINFORCEMENT OF REACTIVE RESINS WACKER CHEMIE AG (DE) 2007-02-01 WO disclosed
US-20060241294-A1 Protected piperazino group-bearing organoxysilane compound and making method SHIN-ETSU CHEMICAL CO., LTD. 2006-10-26 US disclosed
EP-1714968-A1 Protected piperazino group-bearing organoxysilane compound and making method Shin-Etsu Chemical Co., Ltd. (JP) 2006-10-25 EP disclosed
WO-2006072407-A1 REACTIVE SILICIC ACID SUSPENSIONS WACKER CHEMIE AG (DE) 2006-07-13 WO disclosed
WO-2006061091-A2 HIGHLY REACTIVE $G(A)-AMINOMETHYL-ALKOXYSILANES HAVING IMPROVED STABILITY WACKER CHEMIE AG (DE) 2006-06-15 WO disclosed
WO-2006061090-A1 ALKOXYSILANE-TERMINATED PREPOLYMERS WACKER CHEMIE AG (DE) 2006-06-15 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-20060241294-A1 Protected piperazino group-bearing organoxysilane compound and making method PIEZO1, VCL, VIM CYP1A2 3915/4885CHRM2 4118/4885SLC6A4 3273/4885

“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.