SCHEMBL1477260

SCHEMBL1477260

c1ccc2cc(N(c3ccc4ccccc4c3)c3ccc4ccccc4c3)ccc2c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA1 P00915 2/20 0.46
▸ CA2 P00918 2/20 0.46
▸ CYP2A6 P11509 7/20 0.46
▸ CYP1A2 P05177 4/20 0.46
▸ ALDH1A1 P00352 2/20 0.46
▸ CYP3A4 P08684 2/20 0.46
▸ HSD17B10 Q99714 2/20 0.46
▸ TDP1 Q9NUW8 1/20 0.46
▸ CA7 P43166 1/20 0.46
▸ CA9 Q16790 1/20 0.46
▸ ALOX12 P18054 1/20 0.44
▸ INSR P06213 1/20 0.44
▸ IGF1R P08069 1/20 0.44
▸ HTT P42858 1/20 0.43
▸ NPSR1 Q6W5P4 1/20 0.43
▸ L3MBTL1 Q9Y468 1/20 0.43
▸ ESR1 P03372 1/20 0.41
▸ ESR2 Q92731 1/20 0.41
▸ CES2 O00748 1/20 0.41
▸ CES1 P23141 1/20 0.41

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
SCHEMBL7065103 1.00 CA1 (0.46) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL31390245 1.00 CA1 (0.46) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL23264548 0.97 CYP2A6 (0.44) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL17930261 0.97 CYP2A6 (0.44) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL23264365 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL23264547 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL23264551 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL2538296 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL13020773 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1
SCHEMBL13720810 0.93 ALDH1A1 (0.50) CA1CA2CYP2A6CYP1A2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230375936-A1 COMPOSITION FOR DEVELOPING AND METHOD OF FORMING PATTERN USING THE SAME Lee, Geun Su (KR) 2023-11-23 — — US disclosed
US-8829783-B2 Trinaphthyl monoamine or derivative thereof, organic electroluminescent device using the same, and organic electroluminescent material-containing solution IDEMITSU KOSAN CO., LTD. (JP) 2014-09-09 — — US disclosed
US-8829783-B2 Trinaphthyl monoamine or derivative thereof, organic electroluminescent device using the same, and organic electroluminescent material-containing solution IDEMITSU KOSAN CO., LTD. (JP) 2014-09-09 — — US disclosed
WO-2011041529-A3 TRI-2-NAPHTHYLAMINES ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-08-18 — — WO disclosed
WO-2011041529-A2 TRI-2-NAPHTHYLAMINES ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-04-07 — — WO disclosed
WO-2011041529-A2 TRI-2-NAPHTHYLAMINES ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-04-07 — — WO disclosed
WO-2011041529-A2 TRI-2-NAPHTHYLAMINES ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-04-07 — — WO disclosed
US-7914909-B2 Organic electroluminescent device CANON KABUSHIKI KAISHA (JP) 2011-03-29 — — US disclosed
US-20100156285-A1 TRINAPHTHYL MONOAMINE OR DERIVATIVE THEREOF, ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME, AND ORGANIC ELECTROLUMINESCENT MATERIAL-CONTAINING SOLUTION IDEMITSU KOSAN CO., LTD. (JP) 2010-06-24 — — US disclosed
US-20100156285-A1 TRINAPHTHYL MONOAMINE OR DERIVATIVE THEREOF, ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME, AND ORGANIC ELECTROLUMINESCENT MATERIAL-CONTAINING SOLUTION IDEMITSU KOSAN CO., LTD. (JP) 2010-06-24 — — US disclosed
US-7423168-B2 Reacting allyl starting compound with oxygen nucleophilic agent in presence of transition metal catalyst and monodentate phosphite MITSUBISHI CHEMICAL CORPORATION (JP) 2008-09-09 — — US disclosed
US-7241857-B2 Method for producing allyl compound, and ether or ester compound produced thereby MITSUBISHI CHEMICAL CORPORATION (JP) 2007-07-10 — — US disclosed
US-20070155636-A1 Lubricating oil additive and lubricating oil composition containing the same ADEKA CORPORATION (JP) 2007-07-05 — — US disclosed
US-7173157-B2 Method for producing an allyl compound MITSUBISHI CHEMICAL CORPORATION (JP) 2007-02-06 — — US disclosed
EP-1717298-A1 LUBRICATING OIL ADDITIVE AND LUBRICATING OIL COMPOSITION CONTAINING SAME Adeka Corporation (JP) 2006-11-02 — — EP disclosed
US-7119222-B2 Method for producing allyl compound, and ether or ester compound produced thereby MITSUBISHI CHEMICAL CORPORATION (JP) 2006-10-10 — — US disclosed
US-20060106181-A1 Method for producing allyl compound, and ether or ester compound produced thereby MITSUBISHI CHEMICAL CORPORATION (JP) 2006-05-18 — — US disclosed
US-20050075518-A1 Method for producing allyl compound, and allyl compound produced thereby MITSUBISHI CHEMICAL CORPORATION (JP) 2005-04-07 — — US disclosed
US-20040147757-A1 Method for producing allyl compound, and ether or ester compound produced thereby MITSUBISHI CHEMICAL CORPORATION (JP) 2004-07-29 — — US disclosed
US-20040092777-A1 Method for producing allyl compound MITSUBISHI CHEMICAL CORPORATION (JP) 2004-05-13 — — US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060106181-A1 Method for producing allyl compound, and ether or ester compound produced thereby AGPAT5, TST, AGPAT2 CA1 282/4885CA2 756/4885CYP2A6 177/4885
US-20040147757-A1 Method for producing allyl compound, and ether or ester compound produced thereby AGPAT5, TST, AGPAT2 CA1 282/4885CA2 756/4885CYP2A6 177/4885
US-20100156285-A1 TRINAPHTHYL MONOAMINE OR DERIVATIVE THEREOF, ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME, AND ORGANIC ELECTROLUMINESCENT MATERIAL-CONTAINING SOLUTION MAOA, COMT, MAOB CA1 2557/4885CA2 4756/4885CYP2A6 2742/4885
US-20040092777-A1 Method for producing allyl compound CCNT1, APEX1, REV1 CA1 198/4885CA2 788/4885CYP2A6 1590/4885
US-20050075518-A1 Method for producing allyl compound, and allyl compound produced thereby CCNT1, AOC3, ATL3 CA1 1413/4885CA2 2279/4885CYP2A6 143/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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