Ammonia Solution, Strong

Ammonia Solution, Strong

SCHEMBL329693

CCc1ccccc1F.N

nearest known ligand 0.52

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Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 3/20 0.52
L3MBTL1 Q9Y468 1/20 0.50
LMNA P02545 2/20 0.48
IDO1 P14902 2/20 0.48
ALDH1A1 P00352 3/20 0.47
TSHR P16473 2/20 0.47
NPC1 O15118 1/20 0.47
AOC3 Q16853 1/20 0.47
RIPK1 Q13546 2/20 0.46
GABRA1 P14867 2/20 0.44
GABRB2 P47870 2/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
KDM4E B2RXH2 2/20 0.43
MAPK1 P28482 1/20 0.42
HTT P42858 1/20 0.42
HSD17B10 Q99714 1/20 0.42
PSIP1 O75475 1/20 0.42

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
SCHEMBL29943841 0.97
SCHEMBL138361 0.97
Formaldehyde SCHEMBL27510745 0.92 TAAR1 (0.50) TAAR1L3MBTL1LMNAIDO1ALDH1A1
Methoxymethane SCHEMBL27941731 0.90 IDO1 (0.50) TAAR1L3MBTL1LMNAIDO1ALDH1A1
Bicarbonate SCHEMBL28309385 0.88 ALDH1A1 (0.51) TAAR1L3MBTL1LMNAALDH1A1RIPK1
Ammonia Solution, Strong SCHEMBL6195354 0.80 TAAR1 (0.60) TAAR1LMNAIDO1AOC3RIPK1
Ammonia Solution, Strong SCHEMBL2638008 0.80 GABRA1 (0.55) L3MBTL1LMNAALDH1A1GABRA1GABRB2
Hydrochloric Acid SCHEMBL25289904 0.77 GABRA1 (0.52) L3MBTL1LMNAALDH1A1GABRA1GABRB2
Ammonia Solution, Strong SCHEMBL27498500 0.77 GABRA1 (0.52) L3MBTL1LMNAALDH1A1GABRA1GABRB2
SCHEMBL31030319 0.77

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1680137-B1 Macrocyclic carboxylic acid and acylsulfonamide compound as inhibitor of HCV replication HOFFMANN LA ROCHE (CH) 2012-11-21 EP disclosed
US-8198332-B2 Salicylamide derivatives as nicotinic alpha 7 modulators ROCHE PALO ALTO LLC (US) 2012-06-12 US disclosed
EP-2323971-B1 SALICYLAMIDE DERIVATIVES AS NICOTINIC ALPHA 7 MODULATORS HOFFMANN LA ROCHE (CH) 2012-05-09 EP disclosed
EP-2407470-A2 Macrocyclic carboxylic acids and acylsulfonamides as inhibitors of HCV replication F. Hoffmann-La Roche Ltd. (CH) 2012-01-18 EP disclosed
EP-2323971-A1 SALICYLAMIDE DERIVATIVES AS NICOTINIC ALPHA 7 MODULATORS F. Hoffmann-La Roche AG (CH) 2011-05-25 EP disclosed
US-20100041763-A1 Salicylamide derivatives as nicotinic alpha 7 modulators ROCHE PALO ALTO LLC 2010-02-18 US disclosed
WO-2010018095-A1 SALICYLAMIDE DERIVATIVES AS NICOTINIC ALPHA 7 MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2010-02-18 WO disclosed
US-20090286843-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION HOFFMANN-LA ROCHE INC. 2009-11-19 US disclosed
US-20090111982-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION HOFFMANN-LA ROCHE INC. 2009-04-30 US disclosed
US-20090111969-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION HOFFMANN-LA ROCHE INC. 2009-04-30 US disclosed
US-20090105471-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION HOFFMANN-LA ROCHE INC. 2009-04-23 US disclosed
US-7491794-B2 Macrocyclic compounds as inhibitors of viral replication INTERMUNE, INC. (US) 2009-02-17 US disclosed
EP-1749007-A2 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION Intermune, Inc. (US) 2007-02-07 EP disclosed
EP-1680137-A2 MACROCYCLIC CARBOXYLIC ACIDS AND ACYLSULFONAMIDES AS INHIBITORS OF HCV REPLICATION Intermune, Inc. (US) 2006-07-19 EP disclosed
US-20050267018-A1 Macrocyclic compounds as inhibitors of viral replication HOFFMANN-LA ROCHE INC. 2005-12-01 US disclosed
WO-2005095403-A2 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION INTERMUNE, INC. (US) 2005-10-13 WO disclosed
WO-2005037214-A2 MACROCYCLIC CARBOXYLIC ACIDS AND ACYLSULFONAMIDES AS INHIBITORS OF HCV REPLICATION INTERMUNE, INC. (US) 2005-04-28 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 (6 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-20100041763-A1 Salicylamide derivatives as nicotinic alpha 7 modulators CHRNA7, NAPRT, SIRT7 TAAR1 992/4885L3MBTL1 4412/4885LMNA 1941/4885
US-20090111982-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION EIF2AK2, HAVCR2, ZC3HAV1 TAAR1 4718/4885L3MBTL1 2065/4885LMNA 625/4885
US-20090286843-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION EIF2AK2, HAVCR2, ZC3HAV1 TAAR1 4718/4885L3MBTL1 2065/4885LMNA 625/4885
US-20090111969-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION EIF2AK2, HAVCR2, ZC3HAV1 TAAR1 4718/4885L3MBTL1 2065/4885LMNA 625/4885
US-20050267018-A1 Macrocyclic compounds as inhibitors of viral replication EIF2AK2, HAVCR2, ZC3HAV1 TAAR1 4718/4885L3MBTL1 2065/4885LMNA 625/4885
US-20090105471-A1 MACROCYCLIC COMPOUNDS AS INHIBITORS OF VIRAL REPLICATION EIF2AK2, HAVCR2, ZC3HAV1 TAAR1 4718/4885L3MBTL1 2065/4885LMNA 625/4885

“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.