SCHEMBL14982201

SCHEMBL14982201

CN(C)C(=O)C[Si](C)(C)C

nearest known ligand 0.40

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.40
TSHR P16473 2/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
CHRNB2 P17787 1/20 0.33
CHRNB4 P30926 1/20 0.33
CHRNA4 P43681 1/20 0.33
GAA P10253 3/20 0.32
RXFP1 Q9HBX9 1/20 0.32
HSD17B10 Q99714 2/20 0.31
NFKB1 P19838 1/20 0.30
THPO P40225 1/20 0.30
MAPT P10636 1/20 0.30
APEX1 P27695 1/20 0.30
PMP22 Q01453 1/20 0.30
NR4A2 P43354 1/20 0.30

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
SCHEMBL4754657 0.71 ALDH1A1 (0.32) ALDH1A1
SCHEMBL283475 0.67 ALDH1A1 (0.48) ALDH1A1TSHRCHRNB2CHRNB4CHRNA4
SCHEMBL1191256 0.67 ALDH1A1 (0.63) ALDH1A1TSHRCHRNB2CHRNB4CHRNA4
SCHEMBL26455366 0.65 ALDH1A1 (0.46) ALDH1A1TSHRCHRNB2CHRNB4CHRNA4
SCHEMBL2785008 0.65
SCHEMBL6526896 0.65
SCHEMBL9640 0.65
SCHEMBL97330 0.65
SCHEMBL442427 0.65
SCHEMBL1193 0.65

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210253634-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ALLERGAN GI CORP (US) 2021-08-19 US claimed
US-20200172572-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ALLERGAN GI CORP (US) 2020-06-04 US claimed
US-20170218015-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ALLERGAN GI CORP. 2017-08-03 US claimed
EP-3114132-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF MOTUS THERAPEUTICS, INC. (US) 2017-01-11 EP claimed
WO-2015134567-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF RHYTHM PHARMACEUTICALS, INC. (US) 2015-09-11 WO claimed
US-11911475-B2 Low molecular weight cationic lipids for oligonucleotide delivery SIRNA THERAPEUTICS, INC. (US) 2024-02-27 US disclosed
US-11911475-B2 Low molecular weight cationic lipids for oligonucleotide delivery SIRNA THERAPEUTICS, INC. (US) 2024-02-27 US disclosed
US-20230000989-A1 NOVEL LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY SIRNA THERAPEUTICS, INC. (US) 2023-01-05 US disclosed
US-11413348-B2 Low molecular weight cationic lipids for oligonucleotide delivery SIRNA THEREPEUTICS, INC. (US) 2022-08-16 US disclosed
US-11332745-B2 RNA interference mediated inhibition of prolyl hydroxylase domain 2 (PHD2) gene expression using short interfering nucleic acid (SINA) SIMA THERAPEUTICS, INC. (US) 2022-05-17 US disclosed
US-20210253634-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ALLERGAN GI CORP (US) 2021-08-19 US disclosed
EP-3144015-B1 LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY SIRNA THERAPEUTICS INC (US) 2021-06-02 EP disclosed
US-20130178541-A1 NOVEL LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY BANK OF AMERICA, N.A. 2013-07-11 US disclosed
US-20130178541-A1 NOVEL LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY BANK OF AMERICA, N.A. 2013-07-11 US disclosed
US-20130165500-A1 RNA Interference Mediated Inhibition of Prolyl Hydroxylase Domain 2 (PHD2) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-06-27 US disclosed
US-20130165500-A1 RNA Interference Mediated Inhibition of Prolyl Hydroxylase Domain 2 (PHD2) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-06-27 US disclosed
US-20130150433-A1 RNA Interference Mediated Inhibition of Hepatitis B Virus (HBV) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-06-13 US disclosed
US-20130150433-A1 RNA Interference Mediated Inhibition of Hepatitis B Virus (HBV) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-06-13 US disclosed
US-20130137752-A1 RNA Interference Mediated Inhibition of Catenin (Cadherin-Associated Protein), Beta 1 (CTNNB1) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-05-30 US disclosed
US-20130137752-A1 RNA Interference Mediated Inhibition of Catenin (Cadherin-Associated Protein), Beta 1 (CTNNB1) Gene Expression Using Short Interfering Nucleic Acid (siNA) BANK OF AMERICA, N.A. 2013-05-30 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 (9 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-20130165500-A1 RNA Interference Mediated Inhibition of Prolyl Hydroxylase Domain 2 (PHD2) Gene Expression Using Short Interfering Nucleic Acid (siNA) EGLN2, AGO2, EGLN3 ALDH1A1 1527/4885TSHR 2154/4885L3MBTL1 1565/4885
US-20210253634-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF VIP, IAPP, PROKR1 ALDH1A1 3729/4885TSHR 986/4885L3MBTL1 3469/4885
US-20200172572-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF VIP, IAPP, PROKR1 ALDH1A1 3729/4885TSHR 986/4885L3MBTL1 3469/4885
US-20170218015-A1 PROCESS FOR THE LIQUID PHASE SYNTHESIS OF H-INP-(D)BAL-(D)TRP-PHE-APC-NH2, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF VIP, IAPP, PROKR1 ALDH1A1 3729/4885TSHR 986/4885L3MBTL1 3469/4885
US-20230000989-A1 NOVEL LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY LDLR, LIPC, CETP ALDH1A1 3743/4885TSHR 1936/4885L3MBTL1 172/4885
US-20130178541-A1 NOVEL LOW MOLECULAR WEIGHT CATIONIC LIPIDS FOR OLIGONUCLEOTIDE DELIVERY LDLR, LIPC, CETP ALDH1A1 3743/4885TSHR 1936/4885L3MBTL1 172/4885
US-11332745-B2 RNA interference mediated inhibition of prolyl hydroxylase domain 2 (PHD2) gene expression using short interfering nucleic acid (SINA) EGLN2, EGLN3, EGLN1 ALDH1A1 1024/4885TSHR 4513/4885L3MBTL1 1287/4885
US-11911475-B2 Low molecular weight cationic lipids for oligonucleotide delivery LDLR, APOB, CETP ALDH1A1 4090/4885TSHR 1415/4885L3MBTL1 136/4885
US-11413348-B2 Low molecular weight cationic lipids for oligonucleotide delivery LDLR, APOB, CETP ALDH1A1 4090/4885TSHR 1415/4885L3MBTL1 136/4885

“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.