SCHEMBL9344939

SCHEMBL9344939

CCCCCCCCCc1ccc(O)c(-n2nc3ccccc3n2)c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.55
NPC1 O15118 1/20 0.55
RAB9A P51151 1/20 0.55
KAT8 Q9H7Z6 2/20 0.48
PPARA Q07869 1/20 0.45
ESR1 P03372 2/20 0.44
ADRA2A P08913 2/20 0.44
ADORA3 P0DMS8 2/20 0.44
TACR2 P21452 2/20 0.44
SLC6A2 P23975 2/20 0.44
SLC6A4 P31645 2/20 0.44
SLC6A3 Q01959 2/20 0.44
KDM4E B2RXH2 1/20 0.44
ALDH1A1 P00352 1/20 0.44
SHBG P04278 1/20 0.44
TP53 P04637 1/20 0.44
CYP3A4 P08684 1/20 0.44
HSPD1 P10809 1/20 0.44
ADRB3 P13945 1/20 0.44
HTR2C P28335 1/20 0.44

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
SCHEMBL26658063 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL26658034 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL29706513 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL26658059 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL29360801 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL12755311 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL30573271 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL3677611 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL431307 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA
SCHEMBL26658030 1.00 LMNA (0.55) LMNANPC1RAB9AKAT8PPARA

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
US-20240110120-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY CHEVRON U.S.A. INC. (US) 2024-04-04 US claimed
EP-4281528-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY Chevron U.S.A. Inc. (US) 2023-11-29 EP claimed
WO-2022159358-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY CHEVRON U.S.A. INC. (US) 2022-07-28 WO claimed
US-4129521-A Branched chain nonyl and dodecyl isomeric mixtures of 2-(5'-nonyl, or dodecyl-2'-hydroxyphenyl)benzotriazole as UV stabilizers GAF CORPORATION (US) 1978-12-12 US claimed
US-20240110120-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY CHEVRON U.S.A. INC. (US) 2024-04-04 US disclosed
EP-4281528-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY Chevron U.S.A. Inc. (US) 2023-11-29 EP disclosed
WO-2022159358-A1 METHOD FOR MAKING BASE OIL WITH ENHANCED COLOR STABILITY CHEVRON U.S.A. INC. (US) 2022-07-28 WO disclosed
CN-1031340-C Process for preparing substituted 2H-benzotriazole liquid mixtures CIBA GEIGY AG (CH) 1996-03-20 CN disclosed
EP-0337942-B1 Liquid substituted 2H-benzotriazole mixtures CIBA GEIGY AG (CH) 1994-07-06 EP disclosed
US-5240975-A Photostability CIBA-GEIGY CORPORATION (US) 1993-08-31 US disclosed
US-5095062-A Photostability CIBA-GEIGY CORPORATION (US) 1992-03-10 US disclosed
US-4973701-A LIGHT STABILIZERS FOR PHOTOGRAPHY AND POLYMERS CIBA-GEIGY CORPORATION (US) 1990-11-27 US disclosed
CN-1037337-A Substituted 2H-benzotriazole liquid mixtures CIBA GEIGY AG (CH) 1989-11-22 CN disclosed
EP-0337942-A1 Liquid substituted 2H-benzotriazole mixtures CIBA-GEIGY AG (CH) 1989-10-18 EP disclosed
US-4675352-A PHOTOSTABILITY CIBA-GEIGY CORPORATION (US) 1987-06-23 US disclosed
EP-0189374-A2 Liquid mixtures of 2-(hydroxy-3-branched alkyl-5-methylphenyl)-2H-benzotriazole, process for their preparation and stabilized compositions containing them CIBA-GEIGY AG (CH) 1986-07-30 EP disclosed
US-4587346-A ALKYLATION WITH ALKENE AND ACID CATALYST CIBA-GEIGY CORPORATION (US) 1986-05-06 US disclosed