SCHEMBL10337325

SCHEMBL10337325

COC(=O)c1cc(OC)c(N(C)C)c(OC)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 4/20 0.50
▸ CYP3A4 P08684 2/20 0.49
▸ KDM4E B2RXH2 3/20 0.48
▸ ALDH1A1 P00352 2/20 0.48
▸ CA1 P00915 3/20 0.48
▸ CA2 P00918 3/20 0.48
▸ CA12 O43570 2/20 0.48
▸ CA7 P43166 2/20 0.48
▸ CA9 Q16790 2/20 0.48
▸ CA14 Q9ULX7 2/20 0.48
▸ CNR2 P34972 1/20 0.47
▸ LMNA P02545 4/20 0.47
▸ POLB P06746 2/20 0.47
▸ GFER P55789 2/20 0.47
▸ GAA P10253 1/20 0.47
▸ NFKB1 P19838 1/20 0.47
▸ XDH P47989 1/20 0.47
▸ NFKB2 Q00653 1/20 0.47
▸ RELA Q04206 1/20 0.47
▸ FUT7 Q11130 1/20 0.47

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
SCHEMBL10683918 0.84 MAPT (0.46) MAPTCYP3A4KDM4EALDH1A1CA1
SCHEMBL10428228 0.82 CA1 (0.62) CYP3A4CA1CA2CA12CA7
SCHEMBL10681473 0.80 CA1 (0.52) MAPTCYP3A4KDM4EALDH1A1CA1
SCHEMBL31238916 0.79 CNR2 (0.62) MAPTCYP3A4KDM4EALDH1A1CA1
SCHEMBL11358739 0.78 CA1 (0.50) KDM4EALDH1A1CA1CA2CA12
Methyl Syringate SCHEMBL211747 0.78 MEN1 (0.61) MAPTCYP3A4KDM4EALDH1A1CA1
Syringate SCHEMBL159392 0.78 CA12 (0.67) MAPTCYP3A4KDM4EALDH1A1CA1
SCHEMBL2114318 0.78 KMT2A (0.61) MAPTCYP3A4KDM4EALDH1A1CA1
SCHEMBL11352076 0.77 KDM4E (0.53) MAPTKDM4EALDH1A1CA1CA2
SCHEMBL10683847 0.76 KDM4E (0.53) MAPTCYP3A4KDM4EALDH1A1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4908470-A Process for the methyl-4-(dimethylamino)-3,5-dimethoxybenzoate HOFFMAN-LA ROCHE INC. (US) 1990-03-13 — — US claimed
JP-2000248-A — — None — — JP disclosed
EP-0318825-A3 Process for the preparation of 4-dimethylamino-3,5-dimethoxy-benzoic acid methyl ester F. HOFFMANN-LA ROCHE AG (CH) 1990-08-16 — — EP disclosed
US-4908470-A Process for the methyl-4-(dimethylamino)-3,5-dimethoxybenzoate HOFFMAN-LA ROCHE INC. (US) 1990-03-13 — — US disclosed
US-4908470-A Process for the methyl-4-(dimethylamino)-3,5-dimethoxybenzoate HOFFMAN-LA ROCHE INC. (US) 1990-03-13 — — US disclosed
US-4908470-A Process for the methyl-4-(dimethylamino)-3,5-dimethoxybenzoate HOFFMAN-LA ROCHE INC. (US) 1990-03-13 — — US disclosed
JP-H02248-A PREPARATION OF METHYL-4-(DIMETHYLAMINO)-3,5-DEMETHOXY BENZOATE F HOFFMANN LA ROCHE AG 1990-01-05 — — JP disclosed
EP-0318825-A2 Process for the preparation of 4-dimethylamino-3,5-dimethoxy-benzoic acid methyl ester F. HOFFMANN-LA ROCHE AG (CH) 1989-06-07 — — EP disclosed
US-4792557-A 2,4-diamino-5[4-amino (or dimethylamino)-3,5-dimethoxybenzyl]pyrimidine and antibacterial composition thereof HOFFMAN-LA ROCHE INC. (US) 1988-12-20 — — US disclosed
US-4659818-A Intermediates for benzylpyrimidines HOFFMANN-LA ROCHE INC. (US) 1987-04-21 — — US disclosed
US-4515948-A BACTERICIDES, SULFA DRUG POTENTIATORS HOFFMANN-LA ROCHE INC. (US) 1985-05-07 — — US disclosed
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