SCHEMBL2382846

SCHEMBL2382846

Cc1ccc2[nH]c3c(cc(-c4ccc(Br)cc4Cl)c(=O)n3C)c2c1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HPGD P15428 2/20 0.37
▸ LMNA P02545 1/20 0.37
▸ PTGES O14684 2/20 0.37
▸ HTT P42858 1/20 0.36
▸ MDH2 P40926 1/20 0.36
▸ ALDH1A1 P00352 4/20 0.36
▸ MEN1 O00255 3/20 0.36
▸ KMT2A Q03164 3/20 0.36
▸ KDM4E B2RXH2 2/20 0.36
▸ GLA P06280 1/20 0.36
▸ GAA P10253 1/20 0.36
▸ RXFP1 Q9HBX9 1/20 0.35
▸ POLB P06746 2/20 0.35
▸ NPC1 O15118 1/20 0.35
▸ F2RL3 Q96RI0 1/20 0.34
▸ THRB P10828 1/20 0.34
▸ HAVCR2 Q8TDQ0 1/20 0.34
▸ RIPK2 O43353 1/20 0.34
▸ NOD2 Q9HC29 1/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.33

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
SCHEMBL958804 0.88 F2RL3 (0.46) HPGDLMNAHTTALDH1A1MEN1
SCHEMBL1339108 0.87 PIM1 (0.40) HPGDLMNAPTGESHTTMEN1
SCHEMBL2383709 0.84 KDM4E (0.41) HPGDLMNAHTTMDH2ALDH1A1
SCHEMBL2386231 0.84 ALDH1A1 (0.43) HPGDLMNAHTTALDH1A1MEN1
SCHEMBL2384546 0.83 ALDH1A1 (0.41) HPGDLMNAALDH1A1MEN1KMT2A
SCHEMBL2385245 0.81 MAOB (0.41) HPGDLMNAHTTMDH2ALDH1A1
SCHEMBL3443977 0.81 ACHE (0.48) HPGDHTTALDH1A1MEN1KMT2A
SCHEMBL2383622 0.80 LMNA (0.43) HPGDLMNAMDH2ALDH1A1MEN1
SCHEMBL2383319 0.80 OPRM1 (0.41) HPGDLMNAHTTMDH2ALDH1A1
SCHEMBL2383613 0.78 ALDH1A1 (0.41) HPGDLMNAHTTMDH2ALDH1A1

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
US-8012991-B2 3-(2,4-dimethoxyphenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indole-6-carboxylic acid; gamma-aminobutyric acid modulator; anticarcinogenic, antitumor, antiproliferative agent; amidating a 2-aminoindole with an alpha-substituted-beta-hydroxy-alkyl acrylate SANOFI-AVENTIS (FR) 2011-09-06 — — US disclosed
US-20080214538-A1 Pyridoindolone Derivatives Substituted in the 3-Position by a Phenyl, Their Preparation and Their Application in Therapeutics SANOFI-AVENTIS (FR) 2008-09-04 — — US disclosed
US-7390818-B2 Pyridoindolone derivatives substituted in the 3-position by a phenyl, their preparation and their application in therapeutics SANOFI-AVENTIS (FR) 2008-06-24 — — US disclosed
EP-1556382-B1 3-PHENYL SUBSTITUTED PYRIDOINDOLONE, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI AVENTIS (FR) 2008-05-28 — — EP disclosed
US-20050288318-A1 Pyridoindolone derivatives substituted in the 3-position by a phenyl, their preparation and their application in therapeutics SANOFI-AVENTIS (FR) 2005-12-29 — — US disclosed
EP-1556382-A1 3-PHENYL SUBSTITUTED PYRIDOINDOLONE, PREPARATION AND THERAPEUTIC USE THEREOF Sanofi-Aventis (FR) 2005-07-27 — — EP disclosed
WO-2004041817-A1 3-PHENYL SUBSTITUTED PYRIDOINDOLONE, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI-AVENTIS (FR) 2004-05-21 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050288318-A1 Pyridoindolone derivatives substituted in the 3-position by a phenyl, their preparation and their application in therapeutics PNPO, PDXK, PLPBP HPGD 72/4885LMNA 1421/4885PTGES 761/4885
US-20080214538-A1 Pyridoindolone Derivatives Substituted in the 3-Position by a Phenyl, Their Preparation and Their Application in Therapeutics PNPO, PLPBP, DPYD HPGD 76/4885LMNA 1736/4885PTGES 1075/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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