Fluoride Ion

Fluoride Ion

SCHEMBL1502846

C[N+](c1ccccc1)(c1ccccc1)c1ccccc1.[F-]

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
APOBEC3A P31941 1/20 0.58
APOBEC3G Q9HC16 1/20 0.58
ALDH1A1 P00352 4/20 0.38
TDP1 Q9NUW8 3/20 0.38
KDM4E B2RXH2 1/20 0.38
TSHR P16473 4/20 0.37
ACHE P22303 3/20 0.37
LMNA P02545 1/20 0.37
ALOX12 P18054 1/20 0.37
NOS3 P29474 2/20 0.32
NOS1 P29475 2/20 0.32
CA4 P22748 2/20 0.32
TP53 P04637 1/20 0.32
CA12 O43570 1/20 0.30
CA1 P00915 1/20 0.30
CA2 P00918 1/20 0.30
GLA P06280 1/20 0.30
CA3 P07451 1/20 0.30
CA9 Q16790 1/20 0.30
CA14 Q9ULX7 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
SCHEMBL2230404 0.97 APOBEC3A (0.61) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Iodide SCHEMBL240324 0.93 APOBEC3A (0.67) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Bromide SCHEMBL239525 0.93 APOBEC3A (0.58) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Hydrochloric Acid SCHEMBL236927 0.93 APOBEC3A (0.58) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Water SCHEMBL188487 0.93 APOBEC3A (0.58) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Bromide SCHEMBL14972598 0.88 APOBEC3A (0.52) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
SCHEMBL2150488 0.85 APOBEC3A (0.50) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
SCHEMBL27734056 0.85 APOBEC3A (0.50) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
SCHEMBL27817432 0.83 APOBEC3A (0.48) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E
Perchlorate SCHEMBL2149836 0.81 APOBEC3A (0.46) APOBEC3AAPOBEC3GALDH1A1TDP1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2295484-B1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2018-01-17 EP disclosed
US-9290656-B2 Polymerizable composition for polythiourethane optical material MITSUI CHEMICALS, INC. (JP) 2016-03-22 US disclosed
EP-2341091-B1 POLYMERIZABLE COMPOSITION FOR OPTICAL MATERIAL, OPTICAL MATERIAL, AND METHOD FOR PREPARING THE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2013-12-04 EP disclosed
EP-1988109-B1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2013-05-29 EP disclosed
US-8434866-B2 Polymerizable composition for optical material, optical material, and method for preparing the optical material MITSUI CHEMICALS, INC. (JP) 2013-05-07 US disclosed
US-8304507-B2 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS, INC. (JP) 2012-11-06 US disclosed
US-8206673-B2 Method of preparing boron-nitrogen compounds WILDCAT DISCOVERY TECHNOLOGIES (US) 2012-06-26 US disclosed
US-20110190466-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS, INC. (JP) 2011-08-04 US disclosed
EP-2341091-A1 POLYMERIZABLE COMPOUND FOR OPTICAL MATERIAL, OPTICAL MATERIAL, AND OPTICAL MATERIAL MANUFACTURING METHOD Mitsui Chemicals, Inc. (JP) 2011-07-06 EP disclosed
US-20110112269-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM THE POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS, INC. (JP) 2011-05-12 US disclosed
US-4086253-A 3,3',5,5'-Tetra-substituted diphenoquinone from 2,6-disubstituted phenol by phase-transfer catalysis THE DOW CHEMICAL COMPANY (US) 1978-04-25 US disclosed
US-4061682-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT THE DOW CHEMICAL COMPANY (US) 1977-12-06 US disclosed
US-4028439-A QUATERNARY AMMONIUM SALT AND IMIDAZOLE CATALYSTS THE DOW CHEMICAL COMPANY (US) 1977-06-07 US disclosed
US-4016225-A WITH QUATERNARY AMMONIUM SALT AND 1,4-DIAZABICYCLO(2.2.2)OCTANE CATALYST THE DOW CHEMICAL COMPANY (US) 1977-04-05 US disclosed
US-4014891-A FROM AN ALKALI METAL ARYL MERCAPTIDE AND BROMOCHLOROMETHANE IN A QUATERNARY AMMONIUM SALT THE DOW CHEMICAL COMPANY (US) 1977-03-29 US disclosed
US-4007197-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT AND TERTIARY AMINE CATALYST THE DOW CHEMICAL COMPANY (US) 1977-02-08 US disclosed
US-4001293-A Process for production of γ-halonitriles THE DOW CHEMICAL COMPANY (US) 1977-01-04 US disclosed
US-3996259-A QUATERNARY AMMONIUM OR PHOSPHONIUM SALT THE DOW CHEMICAL COMPANY (US) 1976-12-07 US disclosed
US-3974199-A Process for production of cyclopropylcyanide THE DOW CHEMICAL COMPANY (US) 1976-08-10 US disclosed
US-3972887-A QUATERNARY AMMONIUM SALT CATALYST THE DOW CHEMICAL COMPANY (US) 1976-08-03 US disclosed