SCHEMBL640907

SCHEMBL640907

CCC(=O)CC(O)CC

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL29049624 0.88 SLC22A6 (0.38)
SCHEMBL27521363 0.81
SCHEMBL12863648 0.81
SCHEMBL11735870 0.79 GPR84 (0.43)
SCHEMBL15827907 0.79
SCHEMBL18684491 0.79 CES2 (0.39)
SCHEMBL2593186 0.79 SLC22A6 (0.65)
SCHEMBL4805026 0.79 SLC22A6 (0.65)
SCHEMBL15345278 0.79 CYP2C19 (0.50)
SCHEMBL16705749 0.78 TDP1 (0.47)

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
US-20100249166-A1 DIFFERENTIAL EVAPORATION POTENTIATED DISINFECTANT SYSTEM XY, INC. (US) 2010-09-30 US claimed
EP-2209381-A1 DIFFERENTIAL EVAPORATION POTENTIATED DISINFECTANT SYSTEM XY, LLC (US) 2010-07-28 EP claimed
WO-2009038672-A1 DIFFERENTIAL EVAPORATION POTENTIATED DISINFECTANT SYSTEM XY, INC. (US) 2009-03-26 WO claimed
US-20090076169-A1 Differential evaporation potentiated disinfectant system XY, INC. 2009-03-19 US claimed
CN-105567756-B A kind of method of marine bacteria strain and its amine dehydrogenase catalysis preparation Chiral Amine 厦门大学 2019-06-14 CN disclosed
US-9796870-B2 Stabilizer for aggressive chemicals packaging SEKISUI SPECIALTY CHEMICALS AMERICA, LLC (US) 2017-10-24 US disclosed
EP-2209381-B1 DIFFERENTIAL EVAPORATION POTENTIATED DISINFECTANT SYSTEM XY LLC (US) 2017-08-30 EP disclosed
US-9725562-B2 Modified diene polymer, method for producing same, rubber composition, and pneumatic tire TOYO TIRE & RUBBER CO., LTD. (JP) 2017-08-08 US disclosed
EP-2851359-B1 METHOD FOR PRODUCING 4,4''-DIHYDROXY-M-TERPHENYLS HONSHU CHEMICAL IND (JP) 2017-03-29 EP disclosed
US-20170058142-A1 STABILIZER FOR AGGRESSIVE CHEMICALS PACKAGING SEKISUI SPECIALTY CHEMICALS AMERICA, LLC (US) 2017-03-02 US disclosed
US-9474814-B2 Differential evaporation potentiated disinfectant system XY, LLC (US) 2016-10-25 US disclosed
US-9434704-B2 Compositions and methods for the treatment of neurological degenerative disorders CELLIX BIO PRIVATE LIMITED (IN) 2016-09-06 US disclosed
WO-2007014544-A2 STEREOSELECTIVE SYNTHESIS OF CHIRAL DIOLS JULICH CHIRAL SOLUTIONS GMBH (DE) 2007-02-08 WO disclosed
EP-0741120-B1 Polyalphaolefin dimers having low kinematic viscosities CHEVRON PHILLIPS CHEMICAL CO (US) 2003-03-26 EP disclosed
EP-0678493-B1 Controlled formation of olefin oligomers using boron trifluoride and a hydroxy carbonyl CHEVRON CHEM CO (US) 1998-12-30 EP disclosed
US-5817899-A BRANCHED OCTENE, DECENE AND TETRADECENE DIMERS CHEVRON CHEMICAL COMPANY (US) 1998-10-06 US disclosed
EP-0741120-A1 Polyalphaolefin dimers having low kinematic viscosities CHEVRON CHEMICAL COMPANY (US) 1996-11-06 EP disclosed
EP-0678493-A2 Controlled formation of olefin oligomers using boron trifluoride and a hydroxy carbonyl CHEVRON CHEMICAL COMPANY (US) 1995-10-25 EP disclosed
US-5420373-A USING BORON TRIFLUORIDE AND A HYDROXY CARBONYL PROMOTER CHEVRON CHEMICAL COMPANY (US) 1995-05-30 US disclosed
CN-1023478-C Novel compounds ASTRA AB (SE) 1994-01-12 CN disclosed