Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8467658

O=C(N[Zr+2])C1CCCCC1.[Cl-].[Cl-]

nearest known ligand 0.58

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 17)

geneUniProtsupporting neighboursconfidence
HDAC8 Q9BY41 1/20 0.58
HDAC6 Q9UBN7 1/20 0.58
EPHX1 P07099 1/20 0.48
CES2 O00748 1/20 0.48
CES1 P23141 1/20 0.48
TSHR P16473 2/20 0.45
MAPK1 P28482 1/20 0.45
HSD11B1 P28845 2/20 0.44
MAPT P10636 1/20 0.44
HTT P42858 1/20 0.44
PTPN1 P18031 1/20 0.44
HPGD P15428 1/20 0.44
CCR2 P41597 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.42
HSD17B10 Q99714 1/20 0.42
NAAA Q02083 1/20 0.41
GAA P10253 1/20 0.40

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
SCHEMBL757183 0.77 HDAC8 (0.61) HDAC8HDAC6EPHX1CES2CES1
SCHEMBL12323193 0.76 HDAC8 (0.67) HDAC8HDAC6EPHX1CES2CES1
SCHEMBL7056987 0.76 HDAC8 (0.67) HDAC8HDAC6EPHX1CES2CES1
Hydrochloric Acid SCHEMBL7640270 0.75 HDAC8 (0.58) HDAC8HDAC6EPHX1CES2CES1
Hydrochloric Acid SCHEMBL16166996 0.75 HDAC8 (0.58) HDAC8HDAC6EPHX1CES2CES1
Hydrochloric Acid SCHEMBL8674851 0.75 HDAC8 (0.58) HDAC8HDAC6EPHX1CES2CES1
Hydrochloric Acid SCHEMBL5965284 0.75 HDAC8 (0.58) HDAC8HDAC6EPHX1CES2CES1
SCHEMBL7177409 0.75 HDAC8 (0.58) HDAC8HDAC6EPHX1CES2CES1
SCHEMBL3077769 0.74 HDAC6 (1.00) HDAC8HDAC6EPHX1CES2CES1
SCHEMBL5140992 0.74 HDAC6 (1.00) HDAC8HDAC6EPHX1CES2CES1

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
EP-0892816-A1 POLYMERIZATION PROCESS FOR PRODUCING POLYOLEFIN ELASTOMER, CATION-GENERATING COCATALYST FOR ACTIVATING A METALLOCENE PROCATALYST, POLYOLEFIN ELASTOMER POSSESSING A UNIQUE COMBINATION OF PROPERTIES AND PRODUCTS MANUFACTURED THEREFROM UNIROYAL CHEMICAL COMPANY, Inc. (US) 1999-01-27 EP disclosed
US-5723560-A GROUP 4 OR 5 METAL CATALYST FOR OLEFIN POLYMERIZATION EXXON CHEMICAL PATENTS INC. (US) 1998-03-03 US disclosed
WO-1997038019-A1 POLYMERIZATION PROCESS FOR PRODUCING POLYOLEFIN ELASTOMER, CATION-GENERATING COCATALYST FOR ACTIVATING A METALLOCENE PROCATALYST, POLYOLEFIN ELASTOMER POSSESSING A UNIQUE COMBINATION OF PROPERTIES AND PRODUCTS MANUFACTURED THEREFROM UNIROYAL CHEMICAL COMPANY, INC. (US) 1997-10-16 WO disclosed
EP-0705283-A1 PROCESS FOR PRODUCING AMORPHOUS POLY-$g(a)-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1996-04-10 EP disclosed
US-5504169-A FORMING HIGH MOLECULAR WEIGHT POLYPROPYLENE BY CATALYZING IN PRESENCE OF AN ACTIVATOR AND A TITANIUM CYCLOPENTADIENYL COMPLEXES EXXON CHEMICAL PATENTS INC. (US) 1996-04-02 US disclosed
US-5420217-A Polymerization catalyst and promoter EXXON CHEMICAL PATENTS INC. (US) 1995-05-30 US disclosed
WO-1995000562-A1 PROCESS FOR PRODUCING AMORPHOUS POLY-α-OLEFINS WITH A MONOCYCLOPENTADIENYL TRANSITION METAL CATALYST SYSTEM EXXON CHEMICAL PATENTS INC. (US) 1995-01-05 WO disclosed