SCHEMBL7565263

SCHEMBL7565263

C=C(CCC=C(C)C)C(=O)OC

nearest known ligand 0.45

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.45
ALDH1A1 P00352 3/20 0.43
ALOX15 P16050 2/20 0.43
KDM4E B2RXH2 1/20 0.42
ATM Q13315 1/20 0.42
POLB P06746 1/20 0.41
KMT2A Q03164 2/20 0.40
FNTA P49354 4/20 0.39
FNTB P49356 4/20 0.39
MEN1 O00255 1/20 0.38
CYP3A4 P08684 1/20 0.38
ACHE P22303 1/20 0.37
TRPA1 O75762 1/20 0.37

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
SCHEMBL7566818 0.93 KMT2A (0.53) ALDH1A1ALOX15KDM4EATMKMT2A
SCHEMBL8106737 0.93 KMT2A (0.53) ALDH1A1ALOX15KDM4EATMKMT2A
SCHEMBL7589850 0.93 KMT2A (0.53) ALDH1A1ALOX15KDM4EATMKMT2A
SCHEMBL8103041 0.93 KMT2A (0.53) ALDH1A1ALOX15KDM4EATMKMT2A
SCHEMBL9323493 0.84 ALOX15 (0.49) ALDH1A1ALOX15KDM4EATMPOLB
SCHEMBL7561749 0.81 CYP2D6 (0.47) TSHRALDH1A1ALOX15KDM4EATM
SCHEMBL22558000 0.80 KMT2A (0.38) ALDH1A1ALOX15KMT2AFNTAFNTB
SCHEMBL3709138 0.79 ALDH1A1 (0.47) TSHRALDH1A1ALOX15CYP3A4
SCHEMBL5437325 0.79 ALDH1A1 (0.41) TSHRALDH1A1
SCHEMBL7561321 0.78 ALOX15 (0.42) TSHRALDH1A1ALOX15KDM4EATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1013652-B1 Process for preparation of substituted chromanderivatives BASF AG (DE) 2002-08-14 EP disclosed
US-6136986-A REACTING SUBSTITUTED ACROLEIN COMPOUND WITH ACRYLATES, ACROLEINS, ACROLEIN ACETALS, ALLYL ALCOHOLS OR ALLYL ETHERS TO GIVE 3,4-DIHYDRO-2H-PYRANS, REACTING WITH ACID, FOLLOWED BY REACTING WITH SUBSTITUETED VINYL KETONE, DEHYDROGENATION BASF AKTIENGESELLSCHAFT (DE) 2000-10-24 US disclosed
EP-1013652-A2 Process for preparation of substituted chromanderivatives BASF AKTIENGESELLSCHAFT (DE) 2000-06-28 EP disclosed