Hydrochloric Acid

Hydrochloric Acid

SCHEMBL15412907

PC(CCc1ccccc1)c1ccccc1.[Cl-].[Cl-].[Ni+2]

nearest known ligand 0.46

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 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 3/20 0.41
SLC6A3 known ✓ Q01959 3/20 0.41
ACP3 P15309 1/20 0.46
KCNH2 Q12809 3/20 0.44
SIGMAR1 Q99720 2/20 0.42
SLC6A4 P31645 4/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP19A1 P11511 2/20 0.40
ALDH1A1 P00352 1/20 0.39
HPGD P15428 1/20 0.39
ALOX15 P16050 1/20 0.39
ALOX12 P18054 1/20 0.39
CASP1 P29466 1/20 0.39
HSD17B10 Q99714 1/20 0.39
ANPEP P15144 2/20 0.39
ERAP1 Q9NZ08 2/20 0.39
ERAP2 Q6P179 1/20 0.39
TAAR1 Q96RJ0 2/20 0.39
CYP2A6 P11509 1/20 0.38

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
SCHEMBL197100 0.96 ACP3 (0.48) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
Hydrochloric Acid SCHEMBL7165416 0.94 ACP3 (0.47) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL1398395 0.94 ACP3 (0.47) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL7769635 0.94 ACP3 (0.47) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
Bromide SCHEMBL5510650 0.92 ACP3 (0.46) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL9132059 0.90 ACP3 (0.44) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL5076474 0.88 ACP3 (0.47) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL222542 0.88 ACP3 (0.47) ACP3KCNH2SIGMAR1SLC6A4SLC6A2
SCHEMBL197085 0.83 KCNH2 (0.50) KCNH2SIGMAR1SLC6A4SLC6A2SLC6A3
SCHEMBL15288212 0.82 SIGMAR1 (0.49) KCNH2SIGMAR1CYP19A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9224540-B2 Conductive polymer for solid electrolyte capacitor SOLVAY USA, INC. (US) 2015-12-29 US disclosed
EP-2855554-A2 CONDUCTIVE POLYMER FOR SOLID ELECTROLYTIC CAPACITOR Solvay USA Inc. (US) 2015-04-08 EP disclosed
US-20140014881-A1 CONDUCTIVE POLYMER FOR SOLID ELECTROLYTE CAPACITOR PLEXTRONICS, INC. (US) 2014-01-16 US disclosed
WO-2013181165-A2 CONDUCTIVE POLYMER FOR SOLID ELECTROLYTIC CAPACITOR PLEXTRONICS, INC. (US) 2013-12-05 WO disclosed