SCHEMBL7529658

SCHEMBL7529658

Cc1cccc(/C2=C/CCCCCC2)c1

nearest known ligand 0.47

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CHRNB4 P30926 1/20 0.47
CHRNA3 P32297 1/20 0.47
PSMB5 P28074 3/20 0.44
ACMSD Q8TDX5 2/20 0.43
HTR1A P08908 2/20 0.41
MAPK14 Q16539 1/20 0.39
NPC1 O15118 1/20 0.39
MAPT P10636 1/20 0.39
RAB9A P51151 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
SERPINE1 P05121 1/20 0.39
TDP1 Q9NUW8 1/20 0.38
NISCH Q9Y2I1 1/20 0.38
PAX8 Q06710 2/20 0.38
ACHE P22303 1/20 0.38
PTGS2 P35354 1/20 0.38
HDAC1 Q13547 1/20 0.37
HDAC2 Q92769 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
SCHEMBL7529671 1.00 CHRNB4 (0.47) CHRNB4CHRNA3PSMB5ACMSDHTR1A
SCHEMBL19910204 0.98 CHRNB4 (0.49) CHRNB4CHRNA3PSMB5ACMSDHTR1A
SCHEMBL20567911 0.93 CHRNB4 (0.46) CHRNB4CHRNA3PSMB5ACMSDHTR1A
SCHEMBL28039620 0.83 ACHE (0.46) CHRNB4CHRNA3NPC1RAB9ASMN1; SMN2
SCHEMBL26493779 0.82 RAB9A (0.45) CHRNB4CHRNA3PSMB5ACMSDMAPK14
SCHEMBL8836181 0.79 CHRNB4 (0.55) CHRNB4CHRNA3NPC1MAPTRAB9A
SCHEMBL11670468 0.79 PSMB5 (0.46) PSMB5ACMSDPTGS2HDAC1HDAC2
SCHEMBL16718964 0.79 PSMB5 (0.46) PSMB5ACMSDPTGS2HDAC1HDAC2
SCHEMBL11307172 0.79 PSMB5 (0.46) PSMB5ACMSDPTGS2HDAC1HDAC2
SCHEMBL15823144 0.79 CHRNB4 (0.47) CHRNB4CHRNA3PSMB5ACMSDHTR1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1205246-C Process for preparation of addition products of difunctional telechelic polyolefins from cyclic olefins by olefin metathesis reaction CALIFORNIA TECHNOLOGY UNIV (US) 2005-06-08 CN claimed
EP-0626402-B1 Linear telechelic difunctional polymers and process for their preparation. CALIFORNIA INST OF TECHN (US) 2002-07-31 EP claimed
EP-0857183-B1 PROCESS FOR PREPARATION OF ADDITION PRODUCTS OF DIFUNCTIONAL TELECHELIC POLYOLEFINS FROM CYCLIC OLEFINS BY OLEFIN METATHESIS REACTION CALIFORNIA INST OF TECHN (US) 2001-11-07 EP claimed
US-6143851-A Process for preparation of addition products of difunctional telechelic polyolefins from cyclic olefins by olefin metathesis reaction BP AMOCO CORPORATION (US) 2000-11-07 US claimed
CN-1198754-A Process for preparation of addition products of difunctional telechelic polyolefins from cyclic olefins by olefin metathesis reaction AMOCO CORP (US) 1998-11-11 CN claimed
EP-0857183-A1 PROCESS FOR PREPARATION OF ADDITION PRODUCTS OF DIFUNCTIONAL TELECHELIC POLYOLEFINS FROM CYCLIC OLEFINS BY OLEFIN METATHESIS REACTION AMOCO CORPORATION (US) 1998-08-12 EP claimed
US-5731383-A USED FOR HIGH DENSITY POLYESTERS, POLYAMIDES, POLYUREAS, POLYURETHANES AMOCO CORPORATION (US) 1998-03-24 US claimed
WO-1998006771-A1 PROCESS FOR PREPARATION OF ADDITION PRODUCTS OF DIFUNCTIONAL TELECHELIC POLYOLEFINS FROM CYCLIC OLEFINS BY OLEFIN METATHESIS REACTION AMOCO CORPORATION (US) 1998-02-19 WO claimed
US-5621047-A CATALYTIC CROSS-METATHESIS REACTION OF OLEFINS WITH ALKYL (METH)ACRYLATES YIELDS PURE, UNSATURATED POLYMERS HAVING REACTIVE END GROUPS AMOCO CORPORATION (US) 1997-04-15 US claimed
US-5589548-A Process for preparing difunctional telechelic linear non-crosslinked polyolefins AMOCO CORPORATION (US) 1996-12-31 US claimed
US-5512635-A OLEFIN METATHESIS PROCESS; CROSSLINKING INHIBITION AMOCO CORPORATION (US) 1996-04-30 US claimed
EP-0626402-A2 Process for preparing linear monofunctional and telechelic difunctional polymers and compositions obtained thereby AMOCO CORPORATION (US) 1994-11-30 EP claimed
CN-1205246-C Process for preparation of addition products of difunctional telechelic polyolefins from cyclic olefins by olefin metathesis reaction CALIFORNIA TECHNOLOGY UNIV (US) 2005-06-08 CN disclosed
US-20020111447-A1 Novel end-functionalized polyolefin prepared via ring opening metathesis polymerization in the presence of a novel chain transfer agent, and a process for the preparation of the end-functionalized polyolefin via ring opening metathesis polymerization BAYER CORPORATION 2002-08-15 US disclosed
EP-0626402-B1 Linear telechelic difunctional polymers and process for their preparation. CALIFORNIA INST OF TECHN (US) 2002-07-31 EP disclosed
US-20020077428-A1 PROCESS FOR THE SYNTHESIS OF HYDROXYL-END GROUP FUNCTIONALIZED POLYBUTADIENES BAYER CORPORATION 2002-06-20 US disclosed
US-5589548-A Process for preparing difunctional telechelic linear non-crosslinked polyolefins AMOCO CORPORATION (US) 1996-12-31 US disclosed
US-5559190-A Difunctional telechelic linear non-crosslinked polyolefins AMOCO CORPORATION (US) 1996-09-24 US disclosed
US-5512635-A OLEFIN METATHESIS PROCESS; CROSSLINKING INHIBITION AMOCO CORPORATION (US) 1996-04-30 US disclosed
EP-0626402-A2 Process for preparing linear monofunctional and telechelic difunctional polymers and compositions obtained thereby AMOCO CORPORATION (US) 1994-11-30 EP disclosed