SCHEMBL1707006

SCHEMBL1707006

C=C(C)c1cccc(C(C)(C)OOC(C)(C)c2cccc(C(=C)C)c2)c1

nearest known ligand 0.48

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.47
MAPK1 P28482 1/20 0.47
ALDH1A1 P00352 3/20 0.46
TSHR P16473 2/20 0.46
HTT P42858 2/20 0.46
MAPT P10636 2/20 0.46
LMNA P02545 1/20 0.46
KDM4E B2RXH2 1/20 0.43
CYP1A2 P05177 1/20 0.42
CYP3A4 P08684 1/20 0.42
CYP2D6 P10635 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42

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
SCHEMBL545215 0.95 L3MBTL1 (0.44) L3MBTL1MAPK1ALDH1A1TSHRHTT
SCHEMBL9658863 0.89 L3MBTL1 (0.40) L3MBTL1MAPK1ALDH1A1TSHRHTT
SCHEMBL16703328 0.89 SMN1; SMN2 (0.42) L3MBTL1MAPK1ALDH1A1TSHRHTT
SCHEMBL9874577 0.87 ALDH1A1 (0.52) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL18408453 0.82 ACHE (0.55) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL5079320 0.82 ALDH1A1 (0.41) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL14616390 0.82 ALDH1A1 (0.43) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL4880904 0.81 L3MBTL1 (0.49) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL9865144 0.80 L3MBTL1 (0.47) L3MBTL1ALDH1A1TSHRHTTMAPT
SCHEMBL7247284 0.80 L3MBTL1 (0.47) L3MBTL1ALDH1A1TSHRHTTMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7943685-B2 Composition and method for curing latex compounds R.T. VANDERBILT COMPANY, INC. (US) 2011-05-17 US claimed
EP-1869114-B1 METHOD FOR CURING LATEX COMPOUNDS VANDERBILT CO R T (US) 2010-05-26 EP claimed
EP-1869114-A4 COMPOSITION AND METHOD FOR CURING LATEX COMPOUNDS VANDERBILT CO R T (US) 2008-06-18 EP claimed
EP-1869114-A2 COMPOSITION AND METHOD FOR CURING LATEX COMPOUNDS R.T. Vanderbilt Company, Inc. (US) 2007-12-26 EP claimed
WO-2006113141-A2 COMPOSITION AND METHOD FOR CURING LATEX COMPOUNDS R.T. VANDERBILT COMPANY, INC. (US) 2006-10-26 WO claimed
US-20060235126-A1 COMPOSITION AND METHOD FOR CURING LATEX COMPOUNDS R.T. VANDERBILT COMPANY, INC. (US) 2006-10-19 US claimed
US-10569451-B1 Vulcanization of dip-molded rubber articles with reduced molten media bath times APEX MEDICAL TECHNOLOGIES, INC. (US) 2020-02-25 US disclosed
US-20180333902-A1 VULCANIZATION OF DIP-MOLDED RUBBER ARTICLES WITH REDUCED MOLTEN MEDIA BATH TIMES WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT 2018-11-22 US disclosed
EP-1549476-B1 Method for forming an accelerator-free thin-walled rubber vulcanizates from latex KIMBERLY CLARK CO (US) 2012-04-18 EP disclosed
US-7943685-B2 Composition and method for curing latex compounds R.T. VANDERBILT COMPANY, INC. (US) 2011-05-17 US disclosed
EP-1869114-B1 METHOD FOR CURING LATEX COMPOUNDS VANDERBILT CO R T (US) 2010-05-26 EP disclosed
EP-1869114-A4 COMPOSITION AND METHOD FOR CURING LATEX COMPOUNDS VANDERBILT CO R T (US) 2008-06-18 EP disclosed
US-7374711-B2 Accelerator-free thin-walled rubber vulcanizates from latex APEX MEDICAL TECHNOLOGIES, INC. (US) 2008-05-20 US disclosed
US-6569375-B1 Dipping to get film of latex over outer surface; immersion to cause vulcanization of rubber; molten inorganic salts are nitrates, nitrites, carbonates, sulfates, phosphates, and halides of potassium, sodium and lithium; Pore-free APEX MEDICAL TECHNOLOGIES, INC. 2003-05-27 US disclosed
EP-1276792-A2 VULCANIZATION OF DIP-MOLDED RUBBER ARTICLES WITH MOLTEN MEDIA BATHS APEX MEDICAL TECHNOLOGIES, INC. (US) 2003-01-22 EP disclosed
WO-2001077210-A2 VULCANIZATION OF DIP-MOLDED RUBBER ARTICLES WITH MOLTEN MEDIA BATHS APEX MEDICAL TECHNOLOGIES, INC. (US) 2001-10-18 WO disclosed
US-5910553-A POLYMERIZING (METH)ACRYLATE AND A MONOMER WHICH FORMS FREE RADICALS UPON THERMAL DECOMPOSITION TO GIVE A RUBBER WHICH IS MIXED WITH A THIRD MONOMER, FREE RADICAL POLYMERIZATION; WEATHER RESISTANCE, IMPACT STRENGTH BASF AKTIENGESELLSCHAFT (DE) 1999-06-08 US disclosed
EP-0540103-B1 Peroxide vulcanized rubber composition AKZO NOBEL NV (NL) 1996-02-07 EP disclosed
US-5292815-A With bis(citraconamido) compound AKZO N.V. (NL) 1994-03-08 US disclosed
EP-0540103-A1 Peroxide vulcanized rubber composition Akzo Nobel N.V. (NL) 1993-05-05 EP disclosed