Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5086847

CCCCCCCCC[P+](C)(C)CCCCCCCCC.[Cl-]

nearest known ligand 0.58

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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 14)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 4/20 0.58
TSHR P16473 2/20 0.53
THRB P10828 1/20 0.53
OPRM1 P35372 1/20 0.48
SPHK1 Q9NYA1 1/20 0.44
LMNA P02545 2/20 0.43
GGPS1 O95749 2/20 0.42
ADH1B P00325 1/20 0.41
ADH1C P00326 1/20 0.41
ADH1A P07327 1/20 0.41
ADH4 P08319 1/20 0.41
ADH7 P40394 1/20 0.41
ALDH1A1 P00352 2/20 0.40
HSD17B10 Q99714 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
Hydrochloric Acid SCHEMBL5084820 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL7556604 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5087250 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5092767 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5091937 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5092135 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL23576227 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5087047 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5088313 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Iodide SCHEMBL5087923 0.93 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1

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-3998754-A BACTERICIDES, FUNGICIDES AND ALGICIDES; INTERMEDIATES OF QUATERNARY PHOSPHONIUM CLAYS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1976-12-21 US claimed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
US-4188380-A Surface active quaternary higher dialkyl phosphonium salt biocides and intermediates EXXON RESEARCH & ENGINEERING CO. (US) 1980-02-12 US disclosed
US-3998754-A BACTERICIDES, FUNGICIDES AND ALGICIDES; INTERMEDIATES OF QUATERNARY PHOSPHONIUM CLAYS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1976-12-21 US disclosed