Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2992402

CCCCCCCCOCC(O)C[N+](C)(C)C.[Cl-]

nearest known ligand 0.67

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
USP2 O75604 1/20 0.67
HTT P42858 2/20 0.65
LPAR5 Q9H1C0 4/20 0.56
PRKD3 O94806 1/20 0.53
PRKCG P05129 1/20 0.53
PRKCB P05771 1/20 0.53
PRKCA P17252 1/20 0.53
PRKCH P24723 1/20 0.53
PRKCI P41743 1/20 0.53
PRKCE Q02156 1/20 0.53
PRKCQ Q04759 1/20 0.53
PRKCZ Q05513 1/20 0.53
PRKCD Q05655 1/20 0.53
PRKD1 Q15139 1/20 0.53
SPHK1 Q9NYA1 1/20 0.50
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2C19 P33261 1/20 0.47
RAD52 P43351 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44

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 SCHEMBL9706783 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL9706829 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL9706804 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL9706811 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL9706808 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL6419460 1.00 USP2 (0.67) USP2HTTLPAR5PRKD3PRKCG
SCHEMBL7726473 0.98 USP2 (0.69) USP2HTTLPAR5PRKD3PRKCG
SCHEMBL7722820 0.98 USP2 (0.69) USP2HTTLPAR5PRKD3PRKCG
SCHEMBL19206489 0.98 USP2 (0.69) USP2HTTLPAR5PRKD3PRKCG
Hydrochloric Acid SCHEMBL11590308 0.98 USP2 (0.63) USP2HTTLPAR5PRKD3PRKCG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100168450-A1 NOVEL BRANCHED ALKOXYLATES THOEN JOHAN A 2010-07-01 US claimed
EP-2139833-A1 NOVEL BRANCHED ALKOXYLATES Dow Global Technologies Inc. (US) 2010-01-06 EP claimed
WO-2008134390-A1 NOVEL BRANCHED ALKOXYLATES DOW GLOBAL TECHNOLOGIES INC. (US) 2008-11-06 WO claimed
US-20100179354-A1 NOVEL ALKOXY-ETHERS AND ALKOXYLATES THEREOF THOEN JOHAN A 2010-07-15 US disclosed
US-20100168450-A1 NOVEL BRANCHED ALKOXYLATES THOEN JOHAN A 2010-07-01 US disclosed
EP-2152652-A1 NOVEL ALKYLOXY-ETHERS AND ALKOXYLATES THEREOF Dow Global Technologies Inc. (US) 2010-02-17 EP disclosed
EP-2139833-A1 NOVEL BRANCHED ALKOXYLATES Dow Global Technologies Inc. (US) 2010-01-06 EP disclosed
WO-2008134390-A1 NOVEL BRANCHED ALKOXYLATES DOW GLOBAL TECHNOLOGIES INC. (US) 2008-11-06 WO disclosed
WO-2008134387-A1 NOVEL ALKYLOXY-ETHERS AND ALKOXYLATES THEREOF DOW GLOBAL TECHNOLOGIES INC. (US) 2008-11-06 WO disclosed
US-6392064-B2 REACTING AN ALCOHOL WITH EPICHLOROHYDRIN WITH ALKALI METAL HYDROXIDE AND PHASE TRANSFER CATALYST KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2002-05-21 US disclosed
US-20020004605-A1 Method of synthesizing glycidyl ether compounds in the absence of water and organic solvents KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY 2002-01-10 US disclosed
EP-0222335-B1 NON-BRONZING REDDISH LAKE PIGMENT DAINIPPON INK AND CHEMICALS, INC. (JP) 1992-08-19 EP disclosed
US-4711674-A SURFACE TREATMENT WITH N-(3-ALKOXY-2-HYDROXYPROPYL)TRIALKYL AMMONIUM SALT DAINIPPON INK AND CHEMICALS, INC. (JP) 1987-12-08 US disclosed
EP-0222335-A2 Non-bronzing reddish lake pigment DAINIPPON INK AND CHEMICALS, INC. (JP) 1987-05-20 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-20020004605-A1 Method of synthesizing glycidyl ether compounds in the absence of water and organic solvents TET2, DGAT1, ALKBH3 USP2 3857/4885HTT 1505/4885LPAR5 1629/4885

“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.