SCHEMBL244468

SCHEMBL244468

Cc1ccc(-c2cccc(C(=O)O)n2)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.56
ECE1 P42892 1/20 0.55
KDM4E B2RXH2 3/20 0.55
ALOX15 P16050 1/20 0.55
TSHR P16473 1/20 0.55
ACMSD Q8TDX5 1/20 0.55
TDP1 Q9NUW8 1/20 0.55
CTSA P10619 1/20 0.51
ALDH1A1 P00352 4/20 0.50
ERN1 O75460 1/20 0.48
CTRC Q99895 1/20 0.48
ALPL P05186 1/20 0.46
LMNA P02545 1/20 0.45
BRS3 P32247 1/20 0.44
GAA P10253 1/20 0.44
MAPT P10636 1/20 0.44
HPGD P15428 1/20 0.44
SCN10A Q9Y5Y9 1/20 0.43
MCL1 Q07820 1/20 0.43
KMO O15229 1/20 0.43

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
SCHEMBL30614607 1.00 SMN1; SMN2 (0.56) SMN1; SMN2ECE1KDM4EALOX15TSHR
SCHEMBL17049444 0.91 MCL1 (0.55) SMN1; SMN2ECE1ALDH1A1SCN10AMCL1
SCHEMBL17354389 0.86 CTSA (0.48) SMN1; SMN2ECE1CTSAALDH1A1CTRC
SCHEMBL3207980 0.85 KDM4E (0.59) ECE1KDM4EALOX15TSHRACMSD
SCHEMBL208097 0.85 KDM4E (0.64) ECE1KDM4EALOX15TSHRACMSD
SCHEMBL5208768 0.83 CTSA (0.47) SMN1; SMN2ECE1KDM4ETDP1CTSA
Hydrochloric Acid SCHEMBL29133274 0.83 KDM4E (0.61) ECE1KDM4EALOX15TSHRACMSD
SCHEMBL2553456 0.83 KDM4E (0.52) SMN1; SMN2ECE1KDM4EALOX15TSHR
SCHEMBL4901418 0.82 ALDH1A1 (0.61) SMN1; SMN2KDM4EALDH1A1CTRCGAA
SCHEMBL1137226 0.82 HSD17B14 (0.57) ECE1KDM4EALOX15TSHRACMSD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022125736-A1 A TAUTOMERIC LIGAND ENABLES BIOMIMETIC C-H HYDROXYLATION WITH MOLECULAR OXYGEN THE SCRIPPS RESEARCH INSTITUTE (US) 2022-06-16 WO disclosed
CN-102946882-B Phenylalamine derivatives and as the purposes of non-peptide GLP-1-1 receptor modulators ARGUSINA, INC. (US) 2016-05-18 CN disclosed
US-8748412-B2 Phenylalanine derivatives and their use as non-peptide GLP-1 receptor modulators ARGUSINA BIOSCIENCE INC. (KY) 2014-06-10 US disclosed
CN-102946882-A Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators ARGUSINA INC 2013-02-27 CN disclosed
EP-2531198-A1 PHENYLALANINE DERIVATIVES AND THEIR USE AS NON-PEPTIDE GLP-1 RECEPTOR MODULATORS Argusina Inc. (US) 2012-12-12 EP disclosed
US-20120004198-A1 PHENYLALANINE DERIVATIVES AND THEIR USE AS NON-PEPTIDE GLP-1 RECEPTOR MODULATORS ARGUSINA INC. (US) 2012-01-05 US disclosed
WO-2011097300-A1 PHENYLALANINE DERIVATIVES AND THEIR USE AS NON-PEPTIDE GLP-1 RECEPTOR MODULATORS ARGUSINA, INC. (US) 2011-08-11 WO disclosed
WO-2011094890-A1 PHENYLALANINE DERIVATIVES AND THEIR USE AS NON-PEPTIDE GLP-1 RECEPTOR MODULATORS ARGUSINA INC. (US) 2011-08-11 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-20120004198-A1 PHENYLALANINE DERIVATIVES AND THEIR USE AS NON-PEPTIDE GLP-1 RECEPTOR MODULATORS GLP1R, GIPR, GPR119 SMN1; SMN2 3331/4885ECE1 550/4885KDM4E 1650/4885

“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.