Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6694560

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

nearest known ligand 0.55

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 16)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 3/20 0.55
TSHR P16473 1/20 0.50
THRB P10828 1/20 0.50
OPRM1 P35372 1/20 0.46
SPHK1 Q9NYA1 1/20 0.42
LMNA P02545 1/20 0.42
ADH1B P00325 1/20 0.39
ADH1C P00326 1/20 0.39
ADH1A P07327 1/20 0.39
ADH4 P08319 1/20 0.39
ADH7 P40394 1/20 0.39
MEN1 O00255 1/20 0.39
FAAH O00519 1/20 0.39
MAPK1 P28482 1/20 0.39
KMT2A Q03164 1/20 0.39
TRPM8 Q7Z2W7 1/20 0.39

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 SCHEMBL11529307 1.00 DNM1 (0.55) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5088014 1.00 DNM1 (0.55) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5087633 1.00 DNM1 (0.55) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL1925745 1.00 DNM1 (0.55) DNM1TSHRTHRBOPRM1SPHK1
SCHEMBL30354417 0.97 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
SCHEMBL30340673 0.97 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5088279 0.97 DNM1 (0.50) DNM1TSHRTHRBOPRM1SPHK1
SCHEMBL30341088 0.97 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
SCHEMBL29702655 0.97 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL27990427 0.94 DNM1 (0.50) 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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2865711-A1 Ionic liquids as catalysts for vulcanising fluororubbers as a substitute for conventional but toxic vulcanisation additives LANXESS Deutschland GmbH (DE) 2015-04-29 EP disclosed
US-20040181099-A1 Aromatic ethers and process for producing aromatic ethers NIPPON SHOKUBAI CO., LTD. (JP) 2004-09-16 US disclosed
US-5116481-A ANION-SELECTIVE, SENSITIVE FILM, ELECTRODE CONTAINING THE SAME AND THE USE THEREOF HITACHI, LTD. (JP) 1992-05-26 US disclosed
EP-0079461-B1 PROCESS FOR PREPARING ACETIC ANHYDRIDE AND EVENTUALLY ACETIC ACID HOECHST AKTIENGESELLSCHAFT (DE) 1984-12-05 EP disclosed
EP-0079461-A1 Process for preparing acetic anhydride and eventually acetic acid HOECHST AKTIENGESELLSCHAFT (DE) 1983-05-25 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040181099-A1 Aromatic ethers and process for producing aromatic ethers XDH, FTO, CYP4F8 DNM1 2753/4885TSHR 1258/4885THRB 4191/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.