Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8665386

C(C=Cc1ccccc1)=Cc1ccccc1.C(C=Cc1ccccc1)=Cc1ccccc1.C(C=Cc1ccccc1)=Cc1ccccc1.CC1=C(C)C(C)(C)C([Ti+3])=C1C.[Cl-].[Cl-].[Cl-]

nearest known ligand 0.47

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
MAOB P27338 3/20 0.47
ALDH1A1 P00352 3/20 0.37
ALOX5 P09917 2/20 0.37
MAPK1 P28482 2/20 0.37
TRPA1 O75762 2/20 0.37
LMNA P02545 2/20 0.37
NPC1 O15118 2/20 0.35
RAB9A P51151 2/20 0.35
CYP3A4 P08684 2/20 0.35
HDAC3 O15379 1/20 0.34
HDAC4 P56524 1/20 0.34
HDAC1 Q13547 1/20 0.34
HDAC7 Q8WUI4 1/20 0.34
HDAC2 Q92769 1/20 0.34
HDAC10 Q969S8 1/20 0.34
HDAC11 Q96DB2 1/20 0.34
HDAC8 Q9BY41 1/20 0.34
HDAC6 Q9UBN7 1/20 0.34
HDAC9 Q9UKV0 1/20 0.34
HDAC5 Q9UQL6 1/20 0.34

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
SCHEMBL8664993 0.95 MAOB (0.45) MAOBALDH1A1ALOX5MAPK1TRPA1
SCHEMBL8666431 0.95 MAOB (0.45) MAOBALDH1A1ALOX5MAPK1TRPA1
SCHEMBL8665679 0.91 MAOB (0.41) MAOBALDH1A1ALOX5MAPK1TRPA1
Phenol SCHEMBL8668190 0.91 MAOB (0.41) MAOBALDH1A1ALOX5MAPK1TRPA1
SCHEMBL8664539 0.91 MAOB (0.41) MAOBALDH1A1ALOX5MAPK1TRPA1
Phenol SCHEMBL8666387 0.84 MAOB (0.34) MAOBALDH1A1NPC1RAB9ACYP3A4
SCHEMBL8666141 0.82 NFE2L2 (0.35) ALOX5MAPTPTGS1PTGS2NFE2L2
Hydrochloric Acid SCHEMBL8670117 0.71 CTSD (0.31)
Iodide SCHEMBL1539693 0.71 CTSD (0.33)
Fluoride Ion SCHEMBL1131127 0.71 CTSD (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0767804-B1 POLYMERIZATION PROCESS USING DIENE CONTAINING CATALYSTS DOW CHEMICAL CO (US) 1998-12-09 EP claimed
US-5646084-A OLEFIN POLYMERIZATION USING TITANIUM COMPLEX CATALYST AND ACTIVATING COCATALYST THE DOW CHEMICAL COMPANY (US) 1997-07-08 US claimed
EP-0767804-A1 POLYMERIZATION PROCESS USING DIENE CONTAINING CATALYSTS THE DOW CHEMICAL COMPANY (US) 1997-04-16 EP claimed
US-5543480-A USING GROUP 4 METAL COMPLEXES CONTAINING A DIENE MOIETY THE DOW CHEMICAL COMPANY (US) 1996-08-06 US claimed
WO-1996000742-A1 POLYMERIZATION PROCESS USING DIENE CONTAINING CATALYSTS THE DOW CHEMICAL COMPANY (US) 1996-01-11 WO claimed