Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9714762

Cc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1C#N.[Cl-]

nearest known ligand 0.42

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.42
SNCA P37840 2/20 0.41
KDM4E B2RXH2 4/20 0.34
ALDH1A1 P00352 2/20 0.34
MAPK1 P28482 2/20 0.34
L3MBTL1 Q9Y468 2/20 0.34
GAA P10253 2/20 0.34
FFAR1 O14842 1/20 0.34
HIF1A Q16665 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
CTSB P07858 1/20 0.33
MAOB P27338 3/20 0.33
MAOA P21397 2/20 0.33
CACNA1H O95180 1/20 0.32
APP P05067 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
RXFP1 Q9HBX9 1/20 0.32
HPGD P15428 1/20 0.31
HSD17B10 Q99714 1/20 0.31

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
Hydrochloric Acid SCHEMBL9714581 0.88 TSHR (0.42) TSHRSNCAKDM4EALDH1A1MAPK1
Hydrochloric Acid SCHEMBL5972958 0.80 SNCA (0.49) SNCAL3MBTL1GAAHIF1ACTSB
Bromide SCHEMBL4165247 0.77 SNCA (0.51) SNCAL3MBTL1GAAHIF1ACTSB
Hydrochloric Acid SCHEMBL8424236 0.76 SNCA (0.45) SNCAKDM4EALDH1A1MAPK1GAA
Bromide SCHEMBL31753766 0.76 TRPV4 (0.45) SNCAFFAR1MAOBMAOA
Hydrochloric Acid SCHEMBL1575597 0.74 SNCA (0.53) TSHRSNCAL3MBTL1GAAHIF1A
Bromide SCHEMBL3987551 0.73 SNCA (0.39) SNCAKDM4EALDH1A1TDP1HPGD
Hydrochloric Acid SCHEMBL9714743 0.73 FOLH1 (0.48) TSHRSNCAALDH1A1FFAR1MAOB
SCHEMBL12113905 0.73 TSHR (0.46) TSHRSNCAKDM4EALDH1A1L3MBTL1
Bromide SCHEMBL10655444 0.72 MRGPRX4 (0.45) TSHRSNCAALDH1A1CTSB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5166210-A QUINOLINE DERIVATIVES AS ANTAGONISTS OF LEUKOTRIENE D4 RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1992-11-24 US disclosed
US-5028615-A Treatment of hypersensitivity RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1991-07-02 US disclosed
US-4920133-A Quinoline derivatives and use thereof as antagonists of leukotriene D4 RORER PHARMACEUTICAL CORP. (US) 1990-04-24 US disclosed