SCHEMBL60469

SCHEMBL60469

CC=C1C(=O)CC(C)(C)CC1=O

nearest known ligand 0.47

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 12/20 0.47
MAPT P10636 6/20 0.47
L3MBTL1 Q9Y468 2/20 0.47
MAOA P21397 1/20 0.43
GAA P10253 2/20 0.42
KDM4E B2RXH2 2/20 0.41
POLB P06746 1/20 0.40
HTT P42858 2/20 0.39
GLA P06280 1/20 0.39
KMT2A Q03164 2/20 0.38
TP53 P04637 1/20 0.38
APP P05067 1/20 0.38
NPSR1 Q6W5P4 1/20 0.36
HPGD P15428 1/20 0.36
MDM2 Q00987 1/20 0.36
MEN1 O00255 1/20 0.35
ALPL P05186 1/20 0.35
MAPK1 P28482 1/20 0.35
TDP1 Q9NUW8 1/20 0.35

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
SCHEMBL506231 0.81 ALDH1A1 (0.35) ALDH1A1MAPTL3MBTL1
SCHEMBL7648836 0.77 ALDH1A1 (0.46) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL18871416 0.77 ALDH1A1 (0.46) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL581954 0.77 ALDH1A1 (0.46) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL2324941 0.76
SCHEMBL18871435 0.73 ALDH1A1 (0.43) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL2575397 0.73 ALDH1A1 (0.47) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL7617454 0.72 ALDH1A1 (0.42) ALDH1A1MAPTL3MBTL1MAOAGAA
SCHEMBL13167192 0.71
SCHEMBL4928133 0.69 ALDH1A1 (0.40) ALDH1A1MAPTL3MBTL1MAOAGAA

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 1765 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4395831-A1 COMPOSITIONS AND METHODS FOR SKIPPING EXON 45 IN DUCHENNE MUSCULAR DYSTROPHY Entrada Therapeutics, Inc. (US) 2024-07-10 EP claimed
EP-4395829-A1 COMPOUNDS AND METHODS FOR SKIPPING EXON 44 IN DUCHENNE MUSCULAR DYSTROPHY Entrada Therapeutics, Inc. (US) 2024-07-10 EP claimed
CN-118284434-A Compositions and methods for skipping exon 45 in duchenne muscular dystrophy 恩特拉达治疗学股份有限公司 2024-07-02 CN claimed
CN-118215504-A Compounds and methods for skipping exon 44 in duchenne muscular dystrophy 恩特拉达治疗学股份有限公司 2024-06-18 CN claimed
EP-4359006-A1 ANTISENSE COMPOUNDS AND METHODS FOR TARGETING CUG REPEATS Entrada Therapeutics, Inc. (US) 2024-05-01 EP claimed
CN-117957022-A Antisense compounds and methods for targeting CUG repeats 安卓达治疗股份有限公司 2024-04-30 CN claimed
CN-117915957-A Compositions and methods for modulating mRNA splicing 恩特拉达治疗学股份有限公司 2024-04-19 CN claimed
CN-117897176-A Compositions and methods for modulating tissue distribution of intracellular therapeutic agents 恩特拉达治疗学股份有限公司 2024-04-16 CN claimed
EP-4337264-A1 COMPOSITIONS AND METHODS FOR MODULATING TISSUE DISTRIBUTION OF INTRACELLULAR THERAPEUTICS Entrada Therapeutics, Inc. (US) 2024-03-20 EP claimed
EP-4337263-A1 COMPOSITIONS AND METHODS FOR MODULATING INTERFERON REGULATORY FACTOR-5 (IRF-5) ACTIVITY Entrada Therapeutics, Inc. (US) 2024-03-20 EP claimed
US-6930085-B2 G-type peptides to ameliorate atherosclerosis THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-08-16 US claimed
US-20050164950-A1 Orally administered small peptides synergize statin activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2005-07-28 US claimed
US-6869932-B2 Site-specific preparation of polyethlene glycol-GRF conjugates APPLIED RESEARCH SYSTEMS ARS HOLDING N.V. (NL) 2005-03-22 US claimed
US-20040266671-A1 Orally administered peptides synergize statin activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2004-12-30 US claimed
US-20040254120-A1 Orally administered small peptides synergize statin activity THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2004-12-16 US claimed
US-20040248815-A1 Substituted amino acids as erythropoietin mimetics ORTHO MCNEIL PHARMACEUTICAL, INC. 2004-12-09 US claimed
US-6664230-B1 Amino acid sequence 5 having at least one dextro residue; retains biological activity; elevated serum halflife THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2003-12-16 US claimed
US-20020016350-A1 Substituted amino acids as erythropoietin mimetics CONNOLLY PETER J (US) 2002-02-07 US claimed
US-6310078-B1 MODULATING ERYTHROPOIETIN RECEPTOR, TREATING DISEASE OR CONDITION MEDIATED BY SAID RECEPTOR ORTHO-MCNEIL PHARMACEUTICAL, INC. 2001-10-30 US claimed
US-6306911-B1 ENZYME INHIBITORS ORTHO-MCNEIL PHARMACEUTICAL, INC. 2001-10-23 US 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 (2 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-20020016350-A1 Substituted amino acids as erythropoietin mimetics EPOR, EDNRA, FLT1 ALDH1A1 903/4885MAPT 4161/4885L3MBTL1 3681/4885
US-20040248815-A1 Substituted amino acids as erythropoietin mimetics EPOR, EDNRA, FLT1 ALDH1A1 903/4885MAPT 4161/4885L3MBTL1 3681/4885

“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.