SCHEMBL7744530

SCHEMBL7744530

CCCCCCCCOC(=O)C(N)Cc1ccc(O)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 1/20 0.51
TYR P14679 2/20 0.48
ESR1 P03372 3/20 0.48
LMNA P02545 3/20 0.48
TSHR P16473 2/20 0.48
CYP1A2 P05177 1/20 0.48
CYP2D6 P10635 1/20 0.48
MAPK1 P28482 1/20 0.48
CYP2C19 P33261 1/20 0.48
NR1H2 P55055 1/20 0.48
RNASEL Q05823 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
NR5A1 Q13285 1/20 0.47
ALDH1A1 P00352 3/20 0.46
ADRA2A P08913 2/20 0.46
ADORA3 P0DMS8 2/20 0.46
TACR2 P21452 2/20 0.46
SLC6A2 P23975 2/20 0.46
SLC6A4 P31645 2/20 0.46
SLC6A3 Q01959 2/20 0.46

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
SCHEMBL10522486 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL1270831 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL1270832 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL7744532 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL620469 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL1270996 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL1270995 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL5250954 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL5250950 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR
SCHEMBL11053473 1.00 SLC7A5 (0.51) SLC7A5TYRESR1LMNATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102060968-B Optically active polyurethane-amide material and preparation method thereof UNIV SOUTHEAST 2012-11-14 CN disclosed
CN-102060968-A Optically active polyurethane-amide material and preparation method thereof UNIV SOUTHEAST 2011-05-18 CN disclosed
CN-101210069-A Synthesis for degradable polycarbonate based on tyrosine LEPU BEIJING MEDICAL INSTR CO (CN) 2008-07-02 CN disclosed
CN-101209977-A Synthesis for degradable polycarbonate based on tyrosine LEPU BEIJING MEDICAL INSTR CO (CN) 2008-07-02 CN disclosed
CN-101048139-A Compositions for controlled delivery of pharmaceutically active compounds IDEXX LAB INC (US) 2007-10-03 CN disclosed
US-RE37795-E1 BIOPOLYMERS RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY 2002-07-16 US disclosed
US-RE37160-E1 COUPLING A HYDROXYPHENYL CARBOXYLIC ACID WITH AN L-TYROSINE ESTER IN A WATER-MISCIBLE ORGANIC REACTION SOLVENT CONTAINING A CARBODIIMIDE CAPABLE OF FORMING A WATER-SOLVENT UREA BY-PRODUCT RUTGERS, THE STATE UNIVERSITY 2001-05-01 US disclosed
EP-0824513-B1 IMPROVED SYNTHESIS OF TYROSINE-DERIVED DIPHENOL MONOMERS UNIV RUTGERS (US) 2000-07-19 EP disclosed
EP-0824513-A1 IMPROVED SYNTHESIS OF TYROSINE-DERIVED DIPHENOL MONOMERS RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 1998-02-25 EP disclosed
EP-0824513-A4 1998-02-25 EP disclosed
US-5670602-A MONOMERS FOR POLYCARBONATES RUTGERS, THE STATE UNIVERSITY (US) 1997-09-23 US disclosed
US-5587507-A PURIFICATION BY FORMING WATER SOLUBLE UREA BY-PRODUCT RUTGERS, THE STATE UNIVERSITY (US) 1996-12-24 US disclosed
WO-1996030331-A1 IMPROVED SYNTHESIS OF TYROSINE-DERIVED DIPHENOL MONOMERS RUTGERS, THE STATE UNIVERSITY (US) 1996-10-03 WO disclosed