1,6-Hexanediol

1,6-Hexanediol

SCHEMBL2214301

CC1CN1C(C)C(=O)O.CC1CN1C(C)C(=O)O.OCCCCCCO

nearest known ligand 0.40

Full drug profile on Sugi Atlas →

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SLC6A9 P48067 2/20 0.40
SMN1; SMN2 Q16637 1/20 0.35
GPR84 Q9NQS5 1/20 0.34
FFAR1 O14842 1/20 0.34
FFAR4 Q5NUL3 1/20 0.34
CYP1A2 P05177 1/20 0.32
ACE2 Q9BYF1 1/20 0.31
CHRM1 P11229 1/20 0.30
AKR1A1 P14550 1/20 0.30
CHRM3 P20309 1/20 0.30
HTR2A P28223 1/20 0.30
HTR2C P28335 1/20 0.30
ADRA1A P35348 1/20 0.30
HRH1 P35367 1/20 0.30
DRD3 P35462 1/20 0.30
SLC6A3 Q01959 1/20 0.30
HDAC1 Q13547 1/20 0.30
HDAC2 Q92769 1/20 0.30
TDP1 Q9NUW8 1/20 0.30

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
SCHEMBL1144236 0.84 SLC6A9 (0.46) SLC6A9SMN1; SMN2CYP1A2
Hydrochloric Acid SCHEMBL8401126 0.84 SLC6A9 (0.46) SLC6A9SMN1; SMN2CYP1A2
1,6-Hexanediol SCHEMBL2215578 0.75 GPR84 (0.38) SLC6A9SMN1; SMN2GPR84FFAR1FFAR4
SCHEMBL14514528 0.71 SLC6A9 (0.58) SLC6A9SMN1; SMN2
SCHEMBL6428485 0.71 CYP1A2 (0.35) SLC6A9SMN1; SMN2CYP1A2
SCHEMBL14561807 0.70 SLC6A9 (0.41) SLC6A9HTR2AHTR2C
1,6-Hexanediol SCHEMBL8421542 0.70 GPR84 (0.50) SMN1; SMN2GPR84FFAR1FFAR4ACE2
1,6-Hexanediol SCHEMBL8420383 0.70 GPR84 (0.50) SMN1; SMN2GPR84FFAR1FFAR4ACE2
Hydrochloric Acid SCHEMBL23130607 0.69 SLC6A9 (0.49) SLC6A9SMN1; SMN2
SCHEMBL21910390 0.69 SLC6A9 (0.40) SLC6A9SMN1; SMN2HTR2AHTR2CHDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4347673-B1 COMPOSITION INCLUDING CYCLIC IMIDE-CONTAINING MONOMER AND ORGANOBORANE COMPLEX AND RELATED ARTICLES AND METHODS 3M INNOVATIVE PROPERTIES COMPANY (US) 2024-10-09 EP disclosed
US-20240271021-A1 COMPOSITION INCLUDING CYCLIC IMIDE-CONTAINING MONOMER AND ORGANOBORANE COMPLEX AND RELATED ARTICLES AND METHODS 3M INNOVATIVE PROPERTIES COMPANY 2024-08-15 US disclosed
EP-4347673-A1 COMPOSITION INCLUDING CYCLIC IMIDE-CONTAINING MONOMER AND ORGANOBORANE COMPLEX AND RELATED ARTICLES AND METHODS 3M Innovative Properties Company (US) 2024-04-10 EP disclosed
CN-117412998-A Compositions comprising cyclic imide-containing monomers and organoborane complexes, and related articles and methods 3M创新有限公司 2024-01-16 CN disclosed
WO-2022254369-A1 COMPOSITION INCLUDING CYCLIC IMIDE-CONTAINING MONOMER AND ORGANOBORANE COMPLEX AND RELATED ARTICLES AND METHODS 3M INNOVATIVE PROPERTIES COMPANY (US) 2022-12-08 WO disclosed
US-20190284451-A1 SELF-PRIMING ADHESIVE 3M INNOVATIVE PROPERTIES COMPANY 2019-09-19 US disclosed
EP-3458262-A1 SELF-PRIMING ADHESIVE 3M Innovative Properties Company (US) 2019-03-27 EP disclosed
WO-2017200744-A1 SELF-PRIMING ADHESIVE 3M INNOVATIVE PROPERTIES COMPANY (US) 2017-11-23 WO disclosed
EP-2526159-B1 CROSSLINKABLE ACRYLATE ADHESIVE POLYMER COMPOSITION 3M INNOVATIVE PROPERTIES CO (US) 2014-10-22 EP disclosed
US-8524836-B2 Crosslinkable acrylate adhesive polymer composition 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-09-03 US disclosed
WO-2011090984-A1 CROSSLINKABLE ACRYLATE ADHESIVE POLYMER COMPOSITION 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-07-28 WO disclosed
US-20110178248-A1 CROSSLINKABLE ACRYLATE ADHESIVE POLYMER COMPOSITION 3M INNOVATIVE PROPERTIES COMPANY 2011-07-21 US disclosed
US-20090162680-A1 PROCESS FOR MAKING WOOD LAMINATES USING FAST SETTING ADHESIVES AT AMBIENT TEMPERATURE BORDEN CHEMICAL FOUNDRY, LLC 2009-06-25 US disclosed
EP-1963099-A2 PROCESS FOR MAKING WOOD LAMINATES USING FAST SETTING ADHESIVES AT AMBIENT TEMPERATURE Hexion Specialty Chemicals Research Belgium S.A. (BE) 2008-09-03 EP disclosed
WO-2007056357-A2 PROCESS FOR MAKING WOOD LAMINATES USING FAST SETTING ADHESIVES AT AMBIENT TEMPERATURE HEXION SPECIALTY CHEMICALS INC. (US) 2007-05-18 WO disclosed
US-20070102108-A1 Process for making wood laminates using fast setting adhesives at ambient temperature JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT 2007-05-10 US disclosed
EP-0934344-B1 ORGANOBORANE AMINE COMPLEX INITIATOR SYSTEMS AND POLYMERIZABLE COMPOSITIONS MADE THEREWITH MINNESOTA MINING & MFG (US) 2002-10-23 EP disclosed
EP-0934344-A1 ORGANOBORANE AMINE COMPLEX INITIATOR SYSTEMS AND POLYMERIZABLE COMPOSITIONS MADE THEREWITH MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1999-08-11 EP disclosed
US-5935711-A CURABLE MIXTURE ALSO CONTAINING AZIRIDINE-FUNCTIONAL COMPOUND, AMINE REACTIVE COMPOUND TO LIBERATE BORON COMPONENT AND POLYMERIZABLE ACRYLATE MONOMER(S) 3M INNOVATIVE PROPERTIES COMPANY (US) 1999-08-10 US disclosed
WO-1998017694-A1 ORGANOBORANE AMINE COMPLEX INITIATOR SYSTEMS AND POLYMERIZABLE COMPOSITIONS MADE THEREWITH MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-04-30 WO disclosed