Phenanthroline

Phenanthroline

SCHEMBL2879312

O=[N+]([O-])[O-].O=[N+]([O-])[O-].[Cu+2].c1cnc2c(c1)ccc1cccnc12

nearest known ligand 0.70

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.70
LMNA P02545 5/20 0.70
SMN1; SMN2 Q16637 4/20 0.70
KDM4E B2RXH2 3/20 0.70
HTT P42858 3/20 0.70
TDP1 Q9NUW8 3/20 0.70
CCR1 P32246 3/20 0.70
CCR5 P51681 3/20 0.70
CCR8 P51685 3/20 0.70
HSP90AA1 P07900 2/20 0.70
NFKB1 P19838 2/20 0.70
MMP2 P08253 2/20 0.70
TSHR P16473 2/20 0.70
GMNN O75496 1/20 0.70
TP53 P04637 1/20 0.70
CYP3A4 P08684 1/20 0.70
CYP2D6 P10635 1/20 0.70
MMP9 P14780 1/20 0.70
ALOX15 P16050 1/20 0.70
MMP8 P22894 1/20 0.70

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
Phenanthroline SCHEMBL8686231 1.00 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL8685400 1.00 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL8685991 0.98 MAPT (0.67) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL28271628 0.96 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL8685304 0.96 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL11763405 0.96 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL11763410 0.96 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL8685198 0.96 MAPT (0.70) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL28897939 0.89 MAPT (0.67) MAPTLMNASMN1; SMN2KDM4EHTT
Phenanthroline SCHEMBL1450238 0.88 MAPT (0.64) MAPTLMNASMN1; SMN2KDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108250230-B Refining method of diisopropylamine silane 浙江博瑞电子科技有限公司 2020-09-15 CN claimed
CN-108250230-B Refining method of diisopropylamine silane 浙江博瑞电子科技有限公司 2020-09-15 CN disclosed
US-7847126-B2 prepared by reacting phosphorus halide with organomagnesium compound in presence of copper compound; di(tert-butyl)phenylphosphonium tetrafluoroborate, for example LANXESS DEUTSCHLAND GMBH (DE) 2010-12-07 US disclosed
US-20070299273-A1 prepared by reacting phosphorus halide with organomagnesium compound in presence of copper compound; di(tert-butyl)phenylphosphonium tetrafluoroborate, for example LANXESS DEUTSCHLAND GMBH (DE) 2007-12-27 US disclosed
US-7230136-B2 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2007-06-12 US disclosed
US-5739078-A FOR THERMAL RECORDING PAPERS AND PRESSURE SENSITIVE COPYING PAPERS NIPPON SODA CO., LTD. (JP) 1998-04-14 US disclosed
EP-0735105-A1 NOVEL FLUORAN COMPOUND, INTERMEDIATE, AND CHROMOGENIC RECORDING MATERIAL NIPPON SODA CO., LTD. (JP) 1996-10-02 EP disclosed