SCHEMBL1129944

SCHEMBL1129944

CC(CC(c1ccccc1)c1ccc(O)c(C(=O)O)c1)c1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 2/20 0.49
▸ ALDH1A1 P00352 2/20 0.49
▸ HPGD P15428 2/20 0.49
▸ HSD17B10 Q99714 2/20 0.49
▸ TDP1 Q9NUW8 2/20 0.49
▸ CYP2C9 P11712 1/20 0.49
▸ MEN1 O00255 1/20 0.49
▸ CYP2C19 P33261 1/20 0.49
▸ KMT2A Q03164 1/20 0.49
▸ GRM1 Q13255 1/20 0.49
▸ HNF4A P41235 4/20 0.45
▸ MCL1 Q07820 3/20 0.45
▸ ACMSD Q8TDX5 3/20 0.45
▸ DHFR P00374 1/20 0.45
▸ TRPA1 O75762 3/20 0.44
▸ CSNK2A1 P68400 1/20 0.44
▸ KLKB1 P03952 1/20 0.42
▸ CTSB P07858 1/20 0.42
▸ MMP9 P14780 1/20 0.42
▸ DNMT1 P26358 1/20 0.42

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
SCHEMBL10669269 0.88 ALDH1A1 (0.49) KDM4EALDH1A1HPGDHSD17B10TDP1
Methane SCHEMBL9652566 0.82 KDM4E (0.51) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL1373696 0.80 KDM4E (0.56) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL658651 0.80 KDM4E (0.56) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL5964731 0.78 KDM4E (0.54) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL5885460 0.78 TRPA1 (0.40) KDM4EHPGDHSD17B10CYP2C9MCL1
SCHEMBL9769812 0.78 HNF4A (0.54) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL5885088 0.76 ALDH1A1 (0.57) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL25017789 0.76 KDM4E (0.59) KDM4EALDH1A1HPGDHSD17B10TDP1
SCHEMBL9654462 0.76 ALDH1A1 (0.59) KDM4EALDH1A1HPGDHSD17B10TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8283287-B2 Thermosensitive recording material RICOH COMPANY, LTD. (JP) 2012-10-09 — — US disclosed
EP-2036737-B1 Thermosensitive recording material RICOH CO LTD (JP) 2011-02-16 — — EP disclosed
US-20090075817-A1 THERMOSENSITIVE RECORDING MATERIAL RICOH COMPANY, LTD. (JP) 2009-03-19 — — US disclosed
EP-2036737-A1 Thermosensitive recording material Ricoh Company, Ltd. (JP) 2009-03-18 — — EP disclosed
US-6986979-B2 Microcapsule composition EASTMAN KODAK COMPANY (US) 2006-01-17 — — US disclosed
WO-2005073808-A2 PROCESS OF PRODUCING MICROCAPSULES AND PRODUCT THEREOF EASTMAN KODAK COMPANY (US) 2005-08-11 — — WO disclosed
WO-2005073805-A2 COMPOSITION COMPRISING MICROCAPSULES EASTMAN KODAK COMPANY (US) 2005-08-11 — — WO disclosed
US-20050164116-A1 Microcapsule composition EASTMAN KODAK COMPANY 2005-07-28 — — US disclosed
US-20050161843-A1 Process of producing microcapsules and product thereof EASTMAN KODAK COMPANY 2005-07-28 — — US disclosed
US-20050084790-A1 Color developer composition and imaging element containing same EASTMAN KODAK COMPANY 2005-04-21 — — US disclosed
US-5187143-A Thermographic mixture of basic leuco dye and color developer comprising a zinc salt of terephthaldehydic acid or a composite salt also containing an aromatic acid KANZAKI PAPER MANUFACTURING CO., LTD. (JP) 1993-02-16 — — US disclosed
EP-0262810-B1 SHEET RECORDING MATERIAL CONTAINING DYE-FORMING COMPONENTS Fuji Photo Film Co., Ltd. (JP) 1992-12-09 — — EP disclosed
EP-0482668-A1 Heat sensitive recording material KANZAKI PAPER MANUFACTURING COMPANY LIMITED (JP) 1992-04-29 — — EP disclosed
US-4920091-A CONTAINING SALICYLIC ACID DERIVATIVE AS ELECTRON ACCEPTING COLOR DEVELOPER; STABLE IMAGES FUJI PHOTO FILM CO., LTD. (JP) 1990-04-24 — — US disclosed
US-4918047-A CONTAINING OXYSALICYLIC ACID DERIVATIVE AND ZINC COMPOUND FUJI PHOTO FILM CO., LTD. (JP) 1990-04-17 — — US disclosed
US-4914219-A Process for preparing zinc salt of salicylic acid compound FUJI PHOTO FILM CO., LTD. (JP) 1990-04-03 — — US disclosed
EP-0322091-A2 Process for preparing zinc salt of salicyclic acid compound Fuji Photo Film Co., Ltd. (JP) 1989-06-28 — — EP disclosed
US-4808566-A COLORLESS DYE IS DIMER OF 3-(4-SUBSTITUTED AMINOARYL)-3-(SUBSTITUTED INDOL-3-YL) PHTHALIDE FUJI PHOTO FILM CO., LTD. (JP) 1989-02-28 — — US disclosed
EP-0262810-A2 Sheet recording material containing dye-forming components Fuji Photo Film Co., Ltd. (JP) 1988-04-06 — — EP disclosed
EP-0253666-A2 Heat-sensitive recording material containing dye-forming components FUJI PHOTO FILM CO., LTD. (JP) 1988-01-20 — — EP disclosed
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