SCHEMBL275563

SCHEMBL275563

C[Si](C)(CCCNC(=O)CCl)O[Si](C)(C)CCCNC(=O)CCl

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
TSHR P16473 1/20 0.41
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
FAAH O00519 3/20 0.38
CASP2 P42575 1/20 0.34
HTT P42858 2/20 0.33
HSD17B10 Q99714 1/20 0.33
EGFR P00533 1/20 0.33
GAA P10253 1/20 0.33
NAAA Q02083 1/20 0.32
KDM4E B2RXH2 2/20 0.32
MAPK1 P28482 1/20 0.32
HIF1A Q16665 1/20 0.32
LMNA P02545 2/20 0.32
POLB P06746 1/20 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
SCHEMBL12660498 0.93 MEN1 (0.53) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL276131 0.82 MEN1 (0.39) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL13612087 0.81 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL12660513 0.81 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL18227261 0.79 KDM4E (0.56) ALDH1A1SMN1; SMN2TSHRKDM4EMAPK1
SCHEMBL17398955 0.77 MEN1 (0.34) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL14287509 0.77 MEN1 (0.34) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A
SCHEMBL15713279 0.77 NAAA (0.46) ALDH1A1TSHRMEN1KMT2AFAAH
SCHEMBL18227240 0.75 KMT2A (0.40) ALDH1A1MEN1KMT2A
SCHEMBL5830059 0.75 ALDH1A1 (0.83) ALDH1A1SMN1; SMN2TSHRMEN1KMT2A

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8877829-B2 Process for making cationic hydrophilic siloxanyl monomers BAUSCH & LOMB INCORPORATED (US) 2014-11-04 US disclosed
US-8133512-B2 Drug delivery systems based on catonic siloxanyl macromonomers BAUSCH & LOMB INCORPORATED (US) 2012-03-13 US disclosed
US-8133511-B2 Drug delivery system based on cationic siloxanyl macromonomers BAUSCH & LOMB INCORPORATED (US) 2012-03-13 US disclosed
US-7960447-B2 Cationic end-capped siloxane prepolymer for reduced cross-link density BAUSCH & LOMB INCORPORATED (US) 2011-06-14 US disclosed
US-7934830-B2 High water content silicone hydrogels BAUSCH & LOMB INCORPORATED (US) 2011-05-03 US disclosed
US-20110015298-A1 PROCESS FOR MAKING CATIONIC HYDROPHILIC SILOXANYL MONOMERS SANTARUS, INC. 2011-01-20 US disclosed
US-7759408-B2 Silicon-containing monomers end-capped with polymerizable cationic hydrophilic groups BAUSCH & LOMB INCORPORATED (US) 2010-07-20 US disclosed
US-20090274745-A1 Drug delivery systems based on catonic siloxanyl macromonomers BAUSCH & LOMB INCORPORATED (US) 2009-11-05 US disclosed
US-20090274744-A1 Drug delivery system based on cationic siloxanyl macromonomers BAUSCH & LOMB INCORPORATED (US) 2009-11-05 US disclosed
US-7579021-B2 Drug delivery systems based on degradable cationic siloxanyl macromonomers BAUSCH & LOMB INCORPORATED (US) 2009-08-25 US disclosed
US-20080152540-A1 PACKAGING SOLUTIONS BAUSCH & LOMB INCORPORATED (US) 2008-06-26 US disclosed
US-20080075780-A1 Drug delivery systems based on degradible cationic siloxanyl macromonomers SANTARUS, INC. 2008-03-27 US disclosed
US-20070242215-A1 Cationic end-capped siloxane prepolymer for reduced cross-link density BAUSCH & LOMB INCORPORATED 2007-10-18 US disclosed
US-20070149428-A1 Method of Packaging a Lens BAUSCH & LOMB INCORPORATED (US) 2007-06-28 US disclosed
US-20070142584-A1 Silicon-containing monomers end-capped with polymerizable cationic hydrophilic groups LABORATOIRE CHAUVIN S.A.S. (FR) 2007-06-21 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 (7 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-20070242215-A1 Cationic end-capped siloxane prepolymer for reduced cross-link density VCL, SDC1, SDC2 ALDH1A1 4609/4885SMN1; SMN2 3482/4885TSHR 4384/4885
US-20080152540-A1 PACKAGING SOLUTIONS AQP1, ARGLU1, CRYZ ALDH1A1 4081/4885SMN1; SMN2 3337/4885TSHR 3664/4885
US-20070142584-A1 Silicon-containing monomers end-capped with polymerizable cationic hydrophilic groups STIM1, ORAI1, ORAI3 ALDH1A1 4396/4885SMN1; SMN2 1546/4885TSHR 4492/4885
US-20090274744-A1 Drug delivery system based on cationic siloxanyl macromonomers MSR1, LPXN, SRRM2 ALDH1A1 3479/4885SMN1; SMN2 609/4885TSHR 2302/4885
US-20090274745-A1 Drug delivery systems based on catonic siloxanyl macromonomers MMP13, LPXN, SLC13A2 ALDH1A1 1770/4885SMN1; SMN2 839/4885TSHR 2498/4885
US-20110015298-A1 PROCESS FOR MAKING CATIONIC HYDROPHILIC SILOXANYL MONOMERS ILK, SAMM50, AAAS ALDH1A1 2442/4885SMN1; SMN2 4341/4885TSHR 4765/4885
US-20080075780-A1 Drug delivery systems based on degradible cationic siloxanyl macromonomers MSR1, LPXN, SRRM2 ALDH1A1 3230/4885SMN1; SMN2 877/4885TSHR 1721/4885

“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.