SCHEMBL1995374

SCHEMBL1995374

C=C(C)CCOP(=O)(O)OP(=O)(O)OCCC(C)(O)CC(=O)O

nearest known ligand 0.55

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
BTN3A1 O00481 1/20 0.55
MVD P53602 3/20 0.46
HMGCR P04035 1/20 0.37
CHRM1 P11229 1/20 0.37
TBXA2R P21731 1/20 0.37
ADRA1A P35348 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
Isopentenylpyrophosphate SCHEMBL28012930 0.87 BTN3A1 (0.61) BTN3A1MVDHMGCRCHRM1TBXA2R
Isopentenylpyrophosphate SCHEMBL10944407 0.87 BTN3A1 (0.61) BTN3A1MVDHMGCRCHRM1TBXA2R
Diphosphomelavonate SCHEMBL183248 0.83 MVD (0.64) BTN3A1MVDHMGCRCHRM1TBXA2R
Diphosphomelavonate SCHEMBL29398109 0.83 MVD (0.64) BTN3A1MVDHMGCRCHRM1TBXA2R
Diphosphomelavonate SCHEMBL3272270 0.83 MVD (0.64) BTN3A1MVDHMGCRCHRM1TBXA2R
SCHEMBL4372938 0.81 BTN3A1 (0.59) BTN3A1MVD
SCHEMBL3211424 0.79 BTN3A1 (0.85) BTN3A1MVD
SCHEMBL15258419 0.78 MVD (0.47) MVDHMGCRCHRM1TBXA2RADRA1A
SCHEMBL3215369 0.77 BTN3A1 (0.81) BTN3A1MVD
SCHEMBL1286788 0.76 HMGCR (0.50) MVDHMGCRCHRM1TBXA2RADRA1A

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4525455-A HOMOGENIZING MIXTURE OF PLANT EXTRACTS, HYDROGEN BONDING INHIBITOR AND STABILIZER- USED TO CONVERT MEVALONIC ACID OR ISOPENTENYL PYROPHOSPHATE TO PYRETHRINS REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 1985-06-25 US claimed
US-9453244-B2 Method for producing a monoalkene by enzymatic conversion of an alkyl monoester GLOBAL BIOENERGIES (FR) 2016-09-27 US disclosed
US-20150159177-A1 METHOD FOR PRODUCING A MONOALKENE BY ENZYMATIC CONVERSION OF AN ALKYL MONOESTER GLOBAL BIOENERGIES (FR) 2015-06-11 US disclosed
EP-2867365-A1 PROCESS FOR PRODUCING A C2-C10 MONOALKENE EMPLOYING A TERPENE SYNTHASE OR A PRENYL TRANSFERASE Scientist of Fortune S.A. (LU) 2015-05-06 EP disclosed
WO-2014001517-A1 PROCESS FOR PRODUCING A C2-C10 MONOALKENE EMPLOYING A TERPENE SYNTHASE OR A PRENYL TRANSFERASE SCIENTIST OF FORTUNE S.A. (LU) 2014-01-03 WO disclosed
WO-2011076691-A1 METHOD FOR PRODUCING AN ALKENE COMPRISING THE STEP OF CONVERTING AN ALCOHOL BY AN ENZYMATIC DEHYDRATION STEP MARLIERE PHILIPPE (FR) 2011-06-30 WO disclosed
EP-2336340-A1 Method for producing an alkene comprising the step of converting an alcohol by an enzymatic dehydration step Marliere, Philippe (FR) 2011-06-22 EP disclosed
EP-2336341-A1 Method for producing an alkene comprising the step of converting an alcohol by an enzymatic dehydration step Marliere, Philippe (FR) 2011-06-22 EP disclosed