SCHEMBL9304794

SCHEMBL9304794

CCN(CC(C)C)c1cccc(O)c1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.73
CYP3A4 P08684 2/20 0.73
TSHR P16473 2/20 0.48
OPRM1 P35372 6/20 0.43
OPRK1 P41145 5/20 0.43
OPRD1 P41143 4/20 0.43
ESRRG P62508 1/20 0.42
SLC22A1 O15245 1/20 0.42
HTR7 P34969 2/20 0.41
LMNA P02545 2/20 0.37
CA12 O43570 1/20 0.37
CA2 P00918 1/20 0.37
CA5A P35218 1/20 0.37
CA9 Q16790 1/20 0.37
HSD17B10 Q99714 1/20 0.37
CA14 Q9ULX7 1/20 0.37
CA5B Q9Y2D0 1/20 0.37
ACHE P22303 3/20 0.36
DRD2 P14416 1/20 0.36
DRD1 P21728 1/20 0.36

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
SCHEMBL6908896 0.91 ALDH1A1 (0.63) ALDH1A1CYP3A4TSHROPRM1OPRK1
SCHEMBL7072231 0.87 ALDH1A1 (0.69) ALDH1A1CYP3A4TSHROPRM1OPRK1
SCHEMBL124477 0.85 ALDH1A1 (1.00) ALDH1A1CYP3A4TSHROPRM1HTR7
SCHEMBL29379172 0.85 ALDH1A1 (1.00) ALDH1A1CYP3A4TSHROPRM1HTR7
SCHEMBL9322653 0.84 ALDH1A1 (0.56) ALDH1A1CYP3A4TSHROPRM1OPRK1
Ethane SCHEMBL27716473 0.83 ALDH1A1 (0.96) ALDH1A1CYP3A4TSHROPRM1HTR7
Hydrochloric Acid SCHEMBL11588143 0.83 ALDH1A1 (0.96) ALDH1A1CYP3A4TSHROPRM1HTR7
SCHEMBL28495975 0.82 ALDH1A1 (0.53) ALDH1A1CYP3A4TSHROPRM1OPRK1
SCHEMBL16398249 0.81 ALDH1A1 (0.51) ALDH1A1CYP3A4TSHROPRM1OPRK1
SCHEMBL11505004 0.81 ALDH1A1 (0.46) ALDH1A1CYP3A4TSHRLMNAHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0427572-B1 Process for preparing N-alkylaminophenols and N,N-dialkylaminophenols SUMITOMO CHEMICAL CO (JP) 1994-04-27 EP disclosed
EP-0411817-B1 Process for preparing N-alkyl-substituted aminophenols SUMITOMO CHEMICAL CO (JP) 1994-04-06 EP disclosed
US-5276193-A Reductive alkylation, addition of carboxylic acid to prevent by-product formation SUMITOMO CHEMICAL CO., LTD. (JP) 1994-01-04 US disclosed
US-5202485-A Catalytic reductive alkylation of aminophenol using aldehyde or ketone SUMITOMO CHEMICAL CO., LTD. (JP) 1993-04-13 US disclosed
EP-0427572-A1 Process for preparing N-alkylaminophenols and N,N-dialkylaminophenols SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1991-05-15 EP disclosed
EP-0411817-A2 Process for preparing N-alkyl-substituted aminophenols SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1991-02-06 EP disclosed
US-4665199-A CHROMOGENS FOR HEAT-SENSITIVE OR PRESSURE-SENSITIVE RECORDING SHIN NISSO KAKO CO., LTD. (JP) 1987-05-12 US disclosed
US-4613879-A 3-N-ISOBUTYLETHYLAMINO-6-METHYL-7-PHENYLAMINOFLUORAN SHIN NISSO KAKO CO., LTD. (JP) 1986-09-23 US disclosed