SCHEMBL7561749

SCHEMBL7561749

C=C(CCC=C(C)C)C(=O)OCC

nearest known ligand 0.47

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 1/20 0.47
CYP2C19 P33261 1/20 0.47
ALDH1A1 P00352 4/20 0.44
ALOX15 P16050 2/20 0.44
TSHR P16473 2/20 0.42
GLO1 Q04760 1/20 0.41
KDM4E B2RXH2 1/20 0.40
ATM Q13315 1/20 0.40
POLB P06746 1/20 0.39
TRPV1 Q8NER1 1/20 0.38
KMT2A Q03164 1/20 0.38
NPSR1 Q6W5P4 1/20 0.37
LMNA P02545 1/20 0.37
HSD17B10 Q99714 1/20 0.37
FAAH O00519 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
SCHEMBL8106652 0.93 ALOX15 (0.51) ALDH1A1ALOX15KMT2A
SCHEMBL8093235 0.93 ALOX15 (0.51) ALDH1A1ALOX15KMT2A
SCHEMBL7560775 0.93 ALOX15 (0.51) ALDH1A1ALOX15KMT2A
SCHEMBL7582869 0.93 ALOX15 (0.51) ALDH1A1ALOX15KMT2A
SCHEMBL22558163 0.83 ALOX15 (0.40) CYP2D6CYP2C19ALDH1A1ALOX15TSHR
SCHEMBL7561321 0.82 ALOX15 (0.42) ALDH1A1ALOX15TSHRKDM4EATM
SCHEMBL3771224 0.81 FAAH (0.50) CYP2D6CYP2C19ALDH1A1ALOX15GLO1
SCHEMBL7565263 0.81 TSHR (0.45) ALDH1A1ALOX15TSHRKDM4EATM
SCHEMBL410005 0.81 ALDH1A1 (0.42) CYP2D6CYP2C19ALDH1A1ALOX15TSHR
SCHEMBL3756251 0.81 ALDH1A1 (0.42) CYP2D6CYP2C19ALDH1A1ALOX15TSHR

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