SCHEMBL3053174

SCHEMBL3053174

Cc1ccc2ccccc2c1-c1ncc[nH]1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRA2A P08913 3/20 0.46
ADRA2B P18089 2/20 0.46
ADRA2C P18825 2/20 0.46
NISCH Q9Y2I1 3/20 0.44
MTOR P42345 1/20 0.44
ADK P55263 1/20 0.44
CYP2A6 P11509 3/20 0.43
TSHR P16473 2/20 0.43
CYP1A2 P05177 1/20 0.43
CSNK1A1 P48729 1/20 0.42
TYRO3 Q06418 1/20 0.42
DYRK1B Q9Y463 1/20 0.42
LMNA P02545 2/20 0.39
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
MAPT P10636 2/20 0.39
PLA2G1B P04054 1/20 0.39
HSP90AA1 P07900 1/20 0.39
HTT P42858 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39

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
SCHEMBL7397776 0.82 MAPT (0.50) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL14886220 0.81 CSNK1A1 (0.53) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL8342759 0.81 ADRA2A (0.46) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL27767007 0.80 ADRA2A (0.50) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL9682527 0.78 NISCH (0.54) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL7236355 0.77 ADRA2A (0.46) ADRA2AADRA2BADRA2CNISCHMTOR
SCHEMBL6001368 0.77 NISCH (0.52) ADRA2AADRA2CNISCHMTORADK
SCHEMBL7142096 0.77 NISCH (0.61) ADRA2ANISCHMTORADKCYP1A2
SCHEMBL29986334 0.76 KDM4E (0.49) CYP2A6TSHRCYP1A2LMNAMAPT
SCHEMBL10052072 0.76 KDM4E (0.49) CYP2A6TSHRCYP1A2LMNAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8927082-B2 Optical recording medium and method for manufacturing the same RICOH COMPANY, LTD. (JP) 2015-01-06 US disclosed
US-20100221482-A1 OPTICAL RECORDING MEDIUM AND METHOD FOR MANUFACTURING THE SAME RICOH COMPANY, INC. (JP) 2010-09-02 US disclosed
EP-1986866-A1 OPTICAL RECORDING MEDIUM AND METHOD FOR MANUFACTURING THE SAME Ricoh Company, Ltd. (JP) 2008-11-05 EP disclosed
WO-2007097381-A1 OPTICAL RECORDING MEDIUM AND METHOD FOR MANUFACTURING THE SAME RICOH COMPANY, LTD. (JP) 2007-08-30 WO disclosed
US-7144677-B2 Optical recording method and optical recording medium RICOH COMPANY, LTD. (JP) 2006-12-05 US disclosed
US-20060029886-A1 Optical information recording medium and method of producing the same YASHIRO TOHRU 2006-02-09 US disclosed
US-6960421-B2 Optical recording medium and fabricating method thereof RICOH COMPANY, LTD. (JP) 2005-11-01 US disclosed
US-20050058802-A1 Optical information recording medium and method of producing the same YASHIRO TOHRU (JP) 2005-03-17 US disclosed
EP-0896327-B1 Optical information recording medium and method of producing the same RICOH KK (JP) 2004-07-07 EP disclosed
US-20030215673-A1 Optical recording medium and fabricating method thereof RICOH COMPANY, LTD. (JP) 2003-11-20 US disclosed
EP-1343156-A2 Optical recording medium and fabricating method thereof Ricoh Company (JP) 2003-09-10 EP disclosed
US-20030063539-A1 Optical recording method and optical recording medium RICOH COMPANY, LTD 2003-04-03 US disclosed
US-20030059712-A1 Optical information recording medium and method of producing the same YASHIRO TOHRU (JP) 2003-03-27 US disclosed
EP-1244098-A2 An optical recording method and optical recording medium Ricoh Company (JP) 2002-09-25 EP disclosed
US-6045971-A A LAMINATED SUBSTRATE COMPRISING A LIGHT ABSORPTION LAYER INCLUDING THREE DIFFERENT PHTHALOCYANINE DYES RICOH COMPANY, LTD. (JP) 2000-04-04 US disclosed
US-5968708-A METAL PHTHALOCYANINE WITH MANGANESE, IRON, COBALT, ZINC OR CADMIUM METAL WITH ETHER OR SULFIDE SUBSTITUENTS RICOH COMPANY, LTD. (JP) 1999-10-19 US disclosed
US-5882757-A PHTHALOCYANINE COMPOUND HAVING A THERMAL DECOMPOSITION TEMPERATURE IN A RANGE OF 250.DEGREE C. TO 350.DEGREE. C., AND (B) A PHTHALOCYANINE COMPOUND (II) HAVING A THERMAL DECOMPOSITION TEMPERATURE IN A RANGE OF 350.DEGREE. C. TO RICOH COMPANY, LTD. (JP) 1999-03-16 US disclosed
EP-0896327-A1 Optical information recording medium and method of producing the same Ricoh Company, Ltd. (JP) 1999-02-10 EP disclosed
EP-0818562-A1 Composition for treating copper and copper alloy surfaces and method for the surface treatment MEC CO., Ltd. (JP) 1998-01-14 EP disclosed