Paraben

Paraben

SCHEMBL3365205

O=C(O)c1ccc(O)cc1.O=C(O)c1ccc(O)cc1.OCCO

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.80
CA1 P00915 2/20 0.80
CA12 O43570 1/20 0.80
CA3 P07451 1/20 0.80
TYR P14679 1/20 0.80
DRD1 P21728 1/20 0.80
CA4 P22748 1/20 0.80
CA6 P23280 1/20 0.80
CA5A P35218 1/20 0.80
CA7 P43166 1/20 0.80
CA9 Q16790 1/20 0.80
CA14 Q9ULX7 1/20 0.80
CA5B Q9Y2D0 1/20 0.80
SRD5A2 P31213 2/20 0.70
TSHR P16473 2/20 0.60
TP53 P04637 1/20 0.60
ALDH1A1 P00352 3/20 0.58
BLM P54132 2/20 0.58
KDM4E B2RXH2 1/20 0.58
ABL1 P00519 1/20 0.58

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
Paraben SCHEMBL9464608 1.00 CA2 (0.80) CA2CA1CA12CA3TYR
Terephthalic Acid SCHEMBL27317317 1.00 CA2 (0.80) CA2CA1CA12CA3TYR
Paraben SCHEMBL28303722 0.93 CA2 (0.70) CA2CA1CA12CA3TYR
Paraben SCHEMBL2880234 0.91 CA2 (0.73) CA2CA1CA12CA3TYR
Terephthalic Acid SCHEMBL17727576 0.91 CA12 (0.65) CA2CA1CA12CA3TYR
Terephthalic Acid SCHEMBL6692916 0.89 CA2 (1.00) CA2CA1CA12CA3TYR
Terephthalic Acid SCHEMBL3460105 0.89 CA2 (1.00) CA2CA1CA12CA3TYR
Paraben SCHEMBL5311518 0.89 CA2 (1.00) CA2CA1CA12CA3TYR
Paraben SCHEMBL20500516 0.89 CA2 (1.00) CA2CA1CA12CA3TYR
Paraben SCHEMBL4110 0.89 CA2 (1.00) CA2CA1CA12CA3TYR

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 97 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6486293-B1 Electrophotographic photoconductor and method of producing aromatic polycarbonate resin for use in the photoconductor RICOH COMPANY, LTD. (JP) 2002-11-26 US claimed
US-7691931-B2 Organic-inorganic hybrid material and method of preparing the organic-inorganic hybrid material, and electrophotographic photoreceptor, process cartridge, image forming apparatus and image forming method using the organic-inorganic hybrid material RICOH COMPANY LTD. (JP) 2010-04-06 US disclosed
US-7556902-B2 Aromatic polyester resin, and electrophotographic photoconductor and image forming apparatus using thereof RICOH COMPANY, LTD. (JP) 2009-07-07 US disclosed
EP-1256850-B1 Electrophotographic photoreceptor, method for manufacturing the electrophotographic photoreceptor and image forming apparatus using the electrophotographic photoreceptor RICOH KK (JP) 2008-11-26 EP disclosed
US-7452640-B2 Electrophotographic photoconductor for liquid development, image forming apparatus having the same, and image forming method RICOH COMPANY, LTD. (JP) 2008-11-18 US disclosed
US-7348113-B2 Electrophotographic photoconductor comprising a polycarbonate resin having a dihydroxy diphenyl ether unit RICOH COMPANY, LTD. (JP) 2008-03-25 US disclosed
US-7270924-B2 Electrophotographic photoreceptor, method for manufacturing the electrophotographic photoreceptor, and image forming apparatus and process cartridge using the electrophotographic photoreceptor RICOH COMPANY LIMITED (JP) 2007-09-18 US disclosed
US-7175958-B2 Electrophotographic photoconductor, process for forming an image, image forming apparatus and process cartridge for the same RICOH COMPANY, LTD. (JP) 2007-02-13 US disclosed
US-7127196-B2 Electrophotographic photoreceptor, method for manufacturing the electrophotographic photoreceptor and image forming apparatus using the electrophotographic photoreceptor RICOH COMPANY, LTD. (JP) 2006-10-24 US disclosed
US-7122284-B2 Electrophotographic photoconductor, image forming method and apparatus, and process cartridge using the photoconductor, and long-chain alkyl group containing bisphenol compound and polymer made therefrom RICOH COMPANY, LTD. (JP) 2006-10-17 US disclosed
EP-0260338-A1 Poly (ether amide) compositions from reaction of bis-bicyclic amide acetals with bis- and poly-phenolic materials Ashland Oil, Inc. (US) 1988-03-23 EP disclosed
EP-0250715-A1 Resins from phenolics and oxazolines using phosphorous acid esters as catalysts Ashland Oil, Inc. (US) 1988-01-07 EP disclosed
US-4699970-A Resin from phenolic and oxazoline using phosphorous acid ester as catalyst ASHLAND OIL, INC. (US) 1987-10-13 US disclosed
US-4675371-A Thermoset polymeric composition from poly-oxazoline and alkenyl phosphonic acid ASHLAND OIL, INC. (US) 1987-06-23 US disclosed
EP-0215239-A1 Improved process for preparing poly(ether-amide)polymeric compositions Ashland Oil, Inc. (US) 1987-03-25 EP disclosed
US-4652620-A THERMOSETTING RESINS ASHLAND OIL, INC. (US) 1987-03-24 US disclosed
US-4639505-A Poly (ether amide) composition from reaction of bis bicyclic amide acetal with bis- or poly-phenolic material ASHLAND OIL, INC. (US) 1987-01-27 US disclosed
US-4613662-A Process for catalytic preparation of poly(ether-amide) polymeric composition from oxazoline and polyphenol ASHLAND OIL, INC. (US) 1986-09-23 US disclosed
EP-0148787-A2 Positive type photosensitive resin composition JAPAN SYNTHETIC RUBBER CO., LTD. (JP) 1985-07-17 EP disclosed
US-4430491-A THERMOSETTING, MELTS, PHENOLIC OLIGOMER, COMPOUND WITH AT LEAST TW ASHLAND OIL, INC. (US) 1984-02-07 US disclosed