SCHEMBL6550801

SCHEMBL6550801

C=Cc1ccc(OC(=O)OC(C)C)cc1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP2 P08253 1/20 0.43
MMP9 P14780 1/20 0.43
MMP14 P50281 1/20 0.43
CA12 O43570 1/20 0.39
AKR1B10 O60218 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
AKR1B1 P15121 1/20 0.39
CA7 P43166 1/20 0.39
CA9 Q16790 1/20 0.39
CA14 Q9ULX7 1/20 0.39
MAPT P10636 4/20 0.38
SMN1; SMN2 Q16637 3/20 0.38
KDM4E B2RXH2 2/20 0.38
GLA P06280 1/20 0.38
HTT P42858 1/20 0.38
RECQL P46063 1/20 0.38
ALDH1A1 P00352 2/20 0.38
ALDH1A3 P47895 1/20 0.38
TAS1R3 Q7RTX0 2/20 0.38

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
SCHEMBL4150615 0.89 TAS1R3 (0.36) MMP2MMP9MMP14CA12AKR1B10
SCHEMBL1665621 0.84 ALDH1A3 (0.56) MMP2MMP9MMP14CA12AKR1B10
SCHEMBL6780646 0.84 MAPT (0.40) MMP2MMP9MMP14MAPTSMN1; SMN2
SCHEMBL410299 0.84 KMT2A (0.44) MMP2MMP9MMP14MAPTSMN1; SMN2
SCHEMBL2791741 0.83 ALDH1A1 (0.50) MAPTSMN1; SMN2KDM4EALDH1A1MEN1
SCHEMBL5942242 0.81 PTGS2 (0.43) CA12CA1CA2CA7CA9
SCHEMBL9338606 0.79 MAPT (0.52) MMP2MMP9MMP14CA12AKR1B10
SCHEMBL6272847 0.79 CA2 (0.44) CA2KDM4EGLAALDH1A1TAS1R3
SCHEMBL7079093 0.79 ELANE (0.59) CA2MAPTSMN1; SMN2KDM4EALDH1A1
SCHEMBL10204666 0.79 ELANE (0.46) MAPTSMN1; SMN2KDM4EALDH1A1ALDH1A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0789279-B2 Polymer and resist material WAKO PURE CHEM IND LTD (JP) 2004-12-08 EP disclosed
US-6770780-B1 QUATERNIZATION OF T-BUTYL BROMOACETATE WITH TRI(N-BUTYL)PHOSPHINE TO FORM PHOSPHONIUM SALT; REACTING WITH BASE TO FORM PHOSPHORUS YLIDE; FORMING 2,4,6-TRIS(3', 5'-DI-T-BUTYL-4'-HYDROXYBENZYL)METHYL-STYRENE; HYDROLYSIS JSR CORPORATION (JP) 2004-08-03 US disclosed
EP-0780732-B1 Polymer composition and resist material WAKO PURE CHEM IND LTD (JP) 2003-07-09 EP disclosed
EP-1231205-A1 VINYLPHENYLPROPIONIC ACID DERIVATIVES, PROCESSES FOR PRODUCTION OF THE DERIVATIVES, POLYMERS THEREOF AND RADIOSENSITIVE RESIN COMPOSITIONS JSR Corporation (JP) 2002-08-14 EP disclosed
US-6303264-B1 PROFILE OF PATTERN OF QUARTER MICRON ORDER WITHOUT CAUSING FOOTING, WHILE RETAINING HIGH RESOLUTION ABILITY AND HIGH SENSITIVITY WAKO PURE CHEMICAL INDUSTRIES, LTD (JP) 2001-10-16 US disclosed
EP-0789279-B1 Polymer and resist material WAKO PURE CHEM IND LTD (JP) 2001-03-21 EP disclosed
US-6033826-A POLYHYDROXYSTYRENE DERIVATIVE CONTAINING AN ACETAL OR KETAL GROUP WHICH CAN EASILY BE ELIMINATED IN THE PRESENCE OF AN ACID IN THE MOLECULE AND HAVING A VERY NARROW MOLECULAR WEIGHT DISTRIBUTION GIVES A RESIST MATERIAL WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2000-03-07 US disclosed
US-5976759-A ALKALI SOLUBLE BY HEATING WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1999-11-02 US disclosed
EP-0875787-A1 Method for reducing the substrate dependence of resist Wako Pure Chemical Industries, Ltd. (JP) 1998-11-04 EP disclosed
EP-0789279-A1 Polymer and resist material WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1997-08-13 EP disclosed
EP-0780732-A2 Polymer composition and resist material WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1997-06-25 EP disclosed
EP-0264908-B1 High sensitivity resists having autodecomposition temperatures greater than about 160 C IBM (US) 1996-03-20 EP disclosed
US-5204216-A RADIATION-SENSITIVE MIXTURE BASF AKTIENGESELLSCHAFT (DE) 1993-04-20 US disclosed
US-5035979-A Radiation-sensitive mixture BASF AKTIENGESELLSCHAFT (DE) 1991-07-30 US disclosed
US-5034305-A Mixtures for photoresists of water insolublr binders soluble in alkaline mixtures, compound forming a strong acid and solubility inhibitors BASF AKTIENGESELLSCHAFT (DE) 1991-07-23 US disclosed
US-4931379-A ADDITION POLYMERS HAVING PENDANT ACID-LABILE GROUPS, E.G CARBONATES, AND SIDECHAINS FOR ADDED STABILITY; SEMICONDUCTORS; MICROLITHOGRAPHY INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 1990-06-05 US disclosed
EP-0264908-A2 High sensitivity resists having autodecomposition temperatures greater than about 160 C International Business Machines Corporation (US) 1988-04-27 EP disclosed