Phenothiazine

Phenothiazine

SCHEMBL9715033

C=C(C)C(=O)O.c1ccc2c(c1)Nc1ccccc1S2

nearest known ligand 0.64

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NOX1 Q9Y5S8 14/20 0.64
▸ GAA P10253 8/20 0.64
▸ MAPT P10636 8/20 0.64
▸ MEN1 O00255 5/20 0.64
▸ KMT2A Q03164 5/20 0.64
▸ ALOX15 P16050 3/20 0.64
▸ SNCA P37840 2/20 0.64
▸ CYBB P04839 2/20 0.64
▸ NOX3 Q9HBY0 2/20 0.64
▸ NOX4 Q9NPH5 2/20 0.64
▸ APP P05067 1/20 0.64
▸ TDP1 Q9NUW8 3/20 0.61
▸ POLB P06746 3/20 0.61
▸ BCHE P06276 2/20 0.61
▸ ACHE P22303 2/20 0.61
▸ CYP1A2 P05177 1/20 0.61
▸ CYP3A4 P08684 1/20 0.61
▸ ADORA3 P0DMS8 1/20 0.61
▸ ALOX12 P18054 1/20 0.61
▸ MAOA P21397 1/20 0.61

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
Phenothiazine SCHEMBL9727549 0.94 NOX1 (0.57) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL28750254 0.89 NOX1 (0.71) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL8158378 0.87 NOX1 (0.68) NOX1GAAMAPTMEN1KMT2A
Methacrylic Acid SCHEMBL11115741 0.85 NOX1 (0.48) NOX1GAAMAPTMEN1KMT2A
Thianthrene SCHEMBL8726614 0.85 NOX1 (0.48) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL8158386 0.81 NOX1 (0.65) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL9347283 0.80 NOX1 (0.85) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL27936894 0.80 NOX1 (0.94) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL9483121 0.80 NOX1 (0.63) NOX1GAAMAPTMEN1KMT2A
Phenothiazine SCHEMBL688772 0.80 NOX1 (0.63) NOX1GAAMAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5155253-A Reacting vinyl derivative of first Bronsted acid with labile Bronsted acid in presence of ruthenium catalyst, maintaining concentration below certain level and removing product as formed UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1992-10-13 — — US disclosed
EP-0506070-A2 Transvinylation process for the preparation of thermally labile vinyl compounds and vinyl compounds prepared from thermally labile acids UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1992-09-30 — — EP disclosed
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