SCHEMBL7561935

SCHEMBL7561935

C=C(CCC=C(C)C)C(=O)OCCN(C)C

nearest known ligand 0.41

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 1/20 0.41
CHRM4 P08173 1/20 0.41
CHRM5 P08912 1/20 0.41
CHRM1 P11229 1/20 0.41
CHRNB2 P17787 1/20 0.41
CHRM3 P20309 1/20 0.41
CHRNA4 P43681 1/20 0.41
ALOX15 P16050 2/20 0.39
ALDH1A1 P00352 1/20 0.39
USP2 O75604 1/20 0.38
DNM1 Q05193 1/20 0.37
TSHR P16473 1/20 0.37
KDM4E B2RXH2 1/20 0.35
ATM Q13315 1/20 0.35
POLB P06746 1/20 0.34
SQLE Q14534 1/20 0.34
GGPS1 O95749 2/20 0.34
CBLB Q13191 1/20 0.34
BCHE P06276 1/20 0.33

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
SCHEMBL8108789 0.94 ALDH1A1 (0.45) ALOX15ALDH1A1SQLEGGPS1CBLB
SCHEMBL7567877 0.94 ALDH1A1 (0.45) ALOX15ALDH1A1SQLEGGPS1CBLB
SCHEMBL8106453 0.94 ALDH1A1 (0.45) ALOX15ALDH1A1SQLEGGPS1CBLB
SCHEMBL7584379 0.94 ALDH1A1 (0.45) ALOX15ALDH1A1SQLEGGPS1CBLB
SCHEMBL7561321 0.82 ALOX15 (0.42) ALOX15ALDH1A1TSHRKDM4EATM
SCHEMBL27545231 0.81 CHRM1 (0.50) CHRM2CHRM4CHRM5CHRM1CHRNB2
SCHEMBL7561201 0.81 ALOX15 (0.41) ALOX15ALDH1A1TSHRKDM4EATM
SCHEMBL5604791 0.78 DNM1 (0.50) CHRM2CHRM4CHRM5CHRM1CHRNB2
SCHEMBL7561749 0.78 CYP2D6 (0.47) ALOX15ALDH1A1TSHRKDM4EATM
SCHEMBL8068621 0.77 SQLE (0.50) ALOX15ALDH1A1SQLE

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