SCHEMBL6340510

SCHEMBL6340510

CCc1cc(C[C@](C)(N)C(=O)O)ccc1O

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.74
MAPT P10636 3/20 0.74
ALOX15 P16050 3/20 0.74
HSD17B10 Q99714 3/20 0.74
BLM P54132 2/20 0.74
ALDH1A1 P00352 2/20 0.74
CYP1A2 P05177 2/20 0.74
POLB P06746 2/20 0.74
CYP3A4 P08684 2/20 0.74
HPGD P15428 2/20 0.74
TDP1 Q9NUW8 2/20 0.74
MEN1 O00255 1/20 0.74
USP2 O75604 1/20 0.74
EGFR P00533 1/20 0.74
FYN P06241 1/20 0.74
GAA P10253 1/20 0.74
APEX1 P27695 1/20 0.74
ADRA1A P35348 1/20 0.74
PTGS2 P35354 1/20 0.74
MTOR P42345 1/20 0.74

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
SCHEMBL6340509 1.00 KDM4E (0.74) KDM4EMAPTALOX15HSD17B10BLM
SCHEMBL3872299 0.87 ALDH1A1 (0.64) KDM4EMAPTALOX15HSD17B10BLM
SCHEMBL6341702 0.85 ALOX15 (0.67) KDM4EMAPTALOX15HSD17B10BLM
SCHEMBL6718655 0.85 CYP3A4 (0.67) KDM4EMAPTALOX15HSD17B10BLM
SCHEMBL6341699 0.85 ALOX15 (0.67) KDM4EMAPTALOX15HSD17B10BLM
Methyldopa SCHEMBL29352376 0.85 KDM4E (1.00) KDM4EMAPTALOX15HSD17B10BLM
Methyldopa SCHEMBL30176814 0.85 KDM4E (1.00) KDM4EMAPTALOX15HSD17B10BLM
Methyldopa (Racemic) SCHEMBL196981 0.85 KDM4E (1.00) KDM4EMAPTALOX15HSD17B10BLM
Methyldopa SCHEMBL34003 0.85 KDM4E (1.00) KDM4EMAPTALOX15HSD17B10BLM
Methyldopa SCHEMBL1172822 0.85 KDM4E (1.00) KDM4EMAPTALOX15HSD17B10BLM

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-20050080260-A1 Preparation of prodrugs for selective drug delivery LUMINIDE 2005-04-14 US claimed
US-20050080260-A1 Preparation of prodrugs for selective drug delivery LUMINIDE 2005-04-14 US disclosed
US-6555663-B1 Pharmaceuticals which are activated intracellularly by reaction with cellular electron carriers or free radicals to cause release of a free and active drug molecule MILLS RANDELL LEE (US) 2003-04-29 US disclosed
CN-1089086-C Luminandide medicine MILLS RANDELL L (US) 2002-08-14 CN disclosed
EP-0414730-B1 Chemical Compounds and pharmaceutical compositions capable of releasing a drug MILLS RANDELL L (US) 1999-12-15 EP disclosed
US-5773592-A COMPRISES A CHEMILUMINESCENT MOIETY, A PHOTOCHROMIC MOIETY AND A BIOLOGICALLY ACTIVE AGENT CAPABLE OF BEING RELEASED MILLS RANDELL LEE (US) 1998-06-30 US disclosed
US-5428163-A Luminides; chemiluminescence; redox system, releasing free drug MILLS RANDELL L (US) 1995-06-27 US disclosed
EP-0414730-A4 LUMINIDE AND MACROLUMINIDE CLASS OF PHARMACEUTICALS 1993-06-16 EP disclosed
EP-0414730-A1 LUMINIDE AND MACROLUMINIDE CLASS OF PHARMACEUTICALS Mills, Randell L. (US) 1991-03-06 EP disclosed
CN-1047075-A Luminandide medicine MILLS RANDELL L (US) 1990-11-21 CN disclosed
WO-1989009833-A1 LUMINIDE AND MACROLUMINIDE CLASS OF PHARMACEUTICALS MILLS RANDELL L (US) 1989-10-19 WO disclosed
US-4766110-A INHIBITS ANGIOTENSIN CONVERTING ENZYME, HYPOTENSIVE AGENTS RYAN JAMES W (US) 1988-08-23 US disclosed
EP-0073143-B1 NOVEL COMPLEX AMIDO AND IMIDO DERIVATIVES OF CARBOXYALKYL PEPTIDES AND THIOETHERS AND ETHERS OF PEPTIDES Ryan, James Walter (US) 1985-11-21 EP disclosed
EP-0073143-A2 Novel complex amido and imido derivatives of carboxyalkyl peptides and thioethers and ethers of peptides Ryan, James Walter (US) 1983-03-02 EP disclosed
EP-0048159-A2 Novel carboxyalkyl peptides and thioethers and ethers of peptides as antihypertensive agents UNIVERSITY OF MIAMI (US) 1982-03-24 EP 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-20050080260-A1 Preparation of prodrugs for selective drug delivery APEH, PAH, ALAD KDM4E 3072/4885MAPT 2279/4885ALOX15 30/4885

“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.