SCHEMBL9323722

SCHEMBL9323722

COc1ccc(C[N+](=O)[O-])cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 3/20 0.48
KCNJ1 P48048 1/20 0.47
KCNH2 Q12809 1/20 0.47
FBP1 P09467 1/20 0.47
CA12 O43570 1/20 0.46
CA1 P00915 1/20 0.46
CA2 P00918 1/20 0.46
CA7 P43166 1/20 0.46
CA9 Q16790 1/20 0.46
CA14 Q9ULX7 1/20 0.46
CMA1 P23946 1/20 0.46
AGXT P21549 2/20 0.45
LTA4H P09960 1/20 0.45
TAAR1 Q96RJ0 1/20 0.45
KMT2A Q03164 2/20 0.44
MEN1 O00255 1/20 0.44
MAPT P10636 1/20 0.44
CRHBP P24387 1/20 0.44
CRHR2 Q13324 1/20 0.44
NPC1 O15118 1/20 0.44

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
SCHEMBL9322428 0.82 LOXL2 (0.42) IDO1KCNJ1KCNH2CA12CA1
SCHEMBL490893 0.80 KCNJ1 (0.56) IDO1KCNJ1KCNH2TAAR1MAPT
SCHEMBL11743064 0.79 ALDH1A1 (0.46) KMT2AMEN1MAPTHTTALDH1A1
SCHEMBL3030865 0.77 TAAR1 (0.51) IDO1FBP1CMA1AGXTTAAR1
SCHEMBL7051536 0.77 KCNJ1 (0.54) KCNJ1KCNH2TAAR1MAPTNPC1
SCHEMBL17759030 0.77 NPC1 (0.51) KCNH2CA12CA1CA2CA7
SCHEMBL11236036 0.77 LMNA (0.50) KCNH2CA12CA1CA2CA7
SCHEMBL1036369 0.76 ACHE (0.50) IDO1FBP1AGXTTAAR1KMT2A
SCHEMBL9610841 0.76 CA2 (0.45) IDO1CA2TAAR1KMT2AMEN1
SCHEMBL8329926 0.75 SMN1; SMN2 (0.50) FBP1CA12CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2008152142-A1 2 -AMINOQUINAZOLINE DERIVATIVES AND THEIR THERAPEUTIC USES SOFTCURE PHARMACEUTICALS AB (SE) 2008-12-18 WO disclosed
EP-0359519-B1 A process for producing carbamic acid esters BABCOCK HITACHI KK (JP) 1994-02-02 EP disclosed
EP-0296686-B1 A PROCESS FOR THE PREPARATION OF CARBAMATES SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1992-04-01 EP disclosed
US-5101062-A Reacting an amine, oxygen, a nitro compound, carbon monoxide, and alcohol in the presence of a transition metal catalyst, non-metal halide and water BABCOCK-HITACHI KABUSHIKI KAISHA (JP) 1992-03-31 US disclosed
EP-0359519-A1 A process for producing carbamic acid esters BABCOCK-HITACHI KABUSHIKI KAISHA (JP) 1990-03-21 EP disclosed
EP-0296686-A1 A process for the preparation of carbamates SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1988-12-28 EP disclosed
EP-0086281-B2 PREPARATION OF CARBAMATES USING A PALLADIUM-CONTAINING CATALYST SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1988-10-19 EP disclosed
EP-0086281-B1 PREPARATION OF CARBAMATES USING A PALLADIUM-CONTAINING CATALYST SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1985-05-15 EP disclosed
US-4474978-A Preparation of carbamates SHELL OIL COMPANY (US) 1984-10-02 US disclosed
EP-0086281-A1 Preparation of carbamates using a palladium-containing catalyst SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1983-08-24 EP disclosed
US-4341898-A DEHYDROGENATION-ISOMERIZATION REACTION IN PRESENCE OF LEWIS ACID AIR PRODUCTS AND CHEMICALS, INC. (US) 1982-07-27 US disclosed
US-4079076-A TREATING NITRO COMPOUNDS WITH PHOSPHORUS TRICHLORIDE IN THE PRESENCE OF PYRIDINE HOFFMANN-LA ROCHE, INC. (US) 1978-03-14 US disclosed
US-4070391-A Process for producing isocyanate from nitro compounds and carbon monoxide using rhodium oxide catalysts ETHYL CORPORATION (US) 1978-01-24 US disclosed
US-4052437-A PROCESS FOR PRODUCING URETHANE FROM NITRO COMPOUNDS, HYDROXYL COMPOUNDS AND CARBON MONOXIDE USING RHODIUM OXIDE CATALYSTS ETHYL CORPORATION (US) 1977-10-04 US disclosed
US-3935219-A Antimicrobial dihalonitromethylisoxazoles PURDUE RESEARCH LABORATORY (US) 1976-01-27 US disclosed