SCHEMBL7190141

SCHEMBL7190141

CCCCC(F)c1ccc(P(=O)(c2cccc(N)c2)c2cccc(N)c2)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 2/20 0.34
▸ LMNA P02545 1/20 0.33
▸ CYP2C9 P11712 2/20 0.31
▸ CYP2C19 P33261 2/20 0.31
▸ GRM2 Q14416 1/20 0.31
▸ CCNT1 O60563 1/20 0.31
▸ CDK9 P50750 1/20 0.31
▸ MEN1 O00255 3/20 0.30
▸ KMT2A Q03164 3/20 0.30
▸ SMN1; SMN2 Q16637 3/20 0.30
▸ KDM4E B2RXH2 2/20 0.30
▸ MAPT P10636 1/20 0.30
▸ RAB9A P51151 1/20 0.30
▸ TP53 P04637 1/20 0.30
▸ CYP1A2 P05177 1/20 0.30
▸ CYP3A4 P08684 1/20 0.30
▸ HSD17B10 Q99714 1/20 0.30
▸ GAA P10253 1/20 0.30
▸ HPGD P15428 1/20 0.30
▸ MAPK1 P28482 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
SCHEMBL7186358 0.81 NPSR1 (0.45) TSHRLMNACYP2C9CYP2C19CCNT1
SCHEMBL7190146 0.74 CYP19A1 (0.36) —
SCHEMBL7180372 0.73 CA1 (0.33) KMT2ACYP3A4
SCHEMBL9688354 0.72 CYP3A4 (0.52) TSHRLMNAKDM4ECYP3A4HSD17B10
SCHEMBL30471399 0.72 CYP3A4 (0.52) TSHRLMNAKDM4ECYP3A4HSD17B10
SCHEMBL23952138 0.71 HPGD (0.47) TSHRLMNAMEN1KMT2ASMN1; SMN2
SCHEMBL4323677 0.71 CYP3A4 (0.39) TSHRLMNACCNT1CDK9MEN1
SCHEMBL21636282 0.70 MAOA (0.52) TSHRLMNAMEN1KMT2AKDM4E
SCHEMBL29881584 0.70 MAOA (0.52) TSHRLMNAMEN1KMT2AKDM4E
SCHEMBL1536240 0.70 MAOA (0.52) TSHRLMNAMEN1KMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6531633-B2 Grignard reaction of bromobenzene substituted with fluoroalkyl group and diphenylphosphinic chloride in an organic solvent and magnesium, followed by nitration in sulfuric and nitric acids and hydrogenation in presence of palladium KWANGJU INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2003-03-11 — — US claimed
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