SCHEMBL21623

SCHEMBL21623

CO[C]1CCN(c2ccccc2F)CC1

nearest known ligand 0.53

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 7/20 0.50
ALDH1A1 P00352 6/20 0.50
HSD17B10 Q99714 2/20 0.49
KDM4E B2RXH2 6/20 0.48
TDP1 Q9NUW8 2/20 0.48
GAA P10253 1/20 0.48
TSHR P16473 5/20 0.47
LMNA P02545 4/20 0.47
MAPK1 P28482 2/20 0.47
POLB P06746 1/20 0.46
KMT2A Q03164 1/20 0.46
HTT P42858 1/20 0.45
TP53 P04637 1/20 0.45
GLA P06280 1/20 0.44

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
SCHEMBL14689798 0.81 HSD17B10 (0.53) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL8910752 0.80 TRPV1 (0.44) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL1057317 0.80 ADRB1 (0.52) SMN1; SMN2ALDH1A1KDM4EGAATSHR
SCHEMBL1361317 0.76 ALDH1A1 (0.54) SMN1; SMN2ALDH1A1HSD17B10KDM4EGAA
SCHEMBL668861 0.75 HTR7 (0.40) SMN1; SMN2ALDH1A1KDM4ETDP1TSHR
SCHEMBL23161511 0.74 SMN1; SMN2 (0.56) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL3042980 0.74 ALDH1A1 (0.56) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL13941994 0.74 SMN1; SMN2 (0.49) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL21624 0.74 NOTUM (0.49) SMN1; SMN2ALDH1A1HSD17B10KDM4ETDP1
SCHEMBL8911501 0.73 CHRNA7 (0.48) SMN1; SMN2ALDH1A1HSD17B10KDM4ELMNA

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 1052 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116606338-A 6' -cyano modified locked nucleosides, nucleotides and nucleic acid polymers 中国人民解放军军事科学院军事医学研究院 2023-08-18 CN claimed
US-20230192751-A1 METHOD FOR THE PREPARATION OF OLIGONUCLEOTIDES THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIV (CA) 2023-06-22 US claimed
EP-3119789-B1 BICYCLIC CARBOCYCLIC NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM IONIS PHARMACEUTICALS INC (US) 2020-04-22 EP claimed
US-10287313-B2 RNA monomers containing 0-acetal levulinyl ester groups and their use in RNA microarrays THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (CA) 2019-05-14 US claimed
EP-2748176-B1 IONIC TAGS FOR SYNTHESIS OF OLIGORIBONUCLEOTIDES THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING / MCGILL UNIV (CA) 2019-04-17 EP claimed
EP-3323414-A1 INHIBITORS OF NEDD8-ACTIVATING ENZYME Millennium Pharmaceuticals, Inc. (US) 2018-05-23 EP claimed
EP-2850092-B1 TRICYCLIC NUCLEIC ACID ANALOGS IONIS PHARMACEUTICALS INC (US) 2017-03-01 EP claimed
US-20160340382-A1 RNA MONOMERS CONTAINING O-ACETAL LEVULINYL ESTER GROUPS AND THEIR USE IN RNA MICROARRAYS THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (CA) 2016-11-24 US claimed
EP-2727915-B1 Synthesis of deuterated catechols and benzo[d][1,3]dioxoles and derivatives thereof CONCERT PHARMACEUTICALS INC (US) 2016-04-13 EP claimed
EP-2334692-B1 RNA MONOMERS CONTAINING O-ACETAL LEVULINYL ESTER GROUPS AND THEIR USE IN RNA MICROARRAYS UNIV MCGILL (CA) 2016-04-13 EP claimed
US-6949639-B1 Oligonucleotide labeling reactants and their use WALLAC OY (FI) 2005-09-27 US claimed
US-20040260080-A1 Oligonucleotide labeling reactants and their use HOVINEN JARI (FI) 2004-12-23 US claimed
WO-2004064745-A2 METHOD OF PREPARATION OF HETEROCYCLIC MOLECULES WITH PHARMACEUTICAL PHARMACEUTICAL EXCIPIENT COSMECEUTICAL AGROCHEMICAL AND INDUSTRIAL USES AUSPEX PHARMACEUTICALS, INC. (US) 2004-08-05 WO claimed
EP-1152010-A2 Oligonucleotide labeling reactants and their use WALLAC OY (FI) 2001-11-07 EP claimed
US-5789562-A STABLE HYBRIDIZATION COMPLEXES WITH NUCLEI ACIDS HOECHST AKTIENGESELLSCHAFT (DE) 1998-08-04 US claimed
US-5721350-A Deuterated nucleosides CHATTOPADHYAYA JYOTI (SE) 1998-02-24 US claimed
EP-0710667-A2 Modified oligonucleotides, their preparation and their use HOECHST AKTIENGESELLSCHAFT (DE) 1996-05-08 EP claimed
EP-0680969-A2 Modified oligonucleotides, their preparation and their use HOECHST AKTIENGESELLSCHAFT (DE) 1995-11-08 EP claimed
EP-0648220-A1 DEUTERATED NUCLEOSIDES CHATTOPADHYAYA, Jyoti (SE) 1995-04-19 EP claimed
WO-1993025566-A1 DEUTERATED NUCLEOSIDES CHATTOPADHYAYA JYOTI (SE) 1993-12-23 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-10287313-B2 RNA monomers containing 0-acetal levulinyl ester groups and their use in RNA microarrays EFTUD2, RNMT, NSUN2 SMN1; SMN2 905/4885ALDH1A1 199/4885HSD17B10 1459/4885
US-20040260080-A1 Oligonucleotide labeling reactants and their use SSU72, LIG4, NSUN2 SMN1; SMN2 1570/4885ALDH1A1 1426/4885HSD17B10 3345/4885
US-20160340382-A1 RNA MONOMERS CONTAINING O-ACETAL LEVULINYL ESTER GROUPS AND THEIR USE IN RNA MICROARRAYS EFTUD2, RNMT, RNGTT SMN1; SMN2 1087/4885ALDH1A1 212/4885HSD17B10 1594/4885
US-20230192751-A1 METHOD FOR THE PREPARATION OF OLIGONUCLEOTIDES POLN, POLRMT, POLI SMN1; SMN2 1452/4885ALDH1A1 4284/4885HSD17B10 4366/4885

“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.