Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3446376

CCCCC(CC)C[n+]1ccc(N(C)C)cc1.[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 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.47
ALDH1A1 P00352 4/20 0.47
CYP3A4 P08684 1/20 0.47
HSD17B10 Q99714 1/20 0.47
CHKA P35790 9/20 0.46
KDM4A O75164 2/20 0.42
KDM2A Q9Y2K7 2/20 0.42
HTT P42858 4/20 0.39
SMN1; SMN2 Q16637 4/20 0.39
NPC1 O15118 1/20 0.39
RAB9A P51151 1/20 0.39
MITF O75030 1/20 0.37
MAPT P10636 1/20 0.37
NR2F2 P24468 1/20 0.37

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
SCHEMBL3447497 0.98 ALDH1A1 (0.48) LMNAALDH1A1CYP3A4HSD17B10CHKA
Bromide SCHEMBL5683015 0.97 CHKA (0.50) LMNAALDH1A1CYP3A4HSD17B10CHKA
Iodide SCHEMBL7861647 0.97 LMNA (0.47) LMNAALDH1A1CYP3A4HSD17B10CHKA
Bromide SCHEMBL6795666 0.95 CHKA (0.49) LMNAALDH1A1CYP3A4HSD17B10CHKA
Hydrochloric Acid SCHEMBL6687261 0.85 CHRM2 (0.40) LMNAALDH1A1CYP3A4HSD17B10HTT
SCHEMBL13061797 0.83 MEN1 (0.52) LMNAALDH1A1CYP3A4HSD17B10HTT
SCHEMBL9834890 0.83 CHRM2 (0.40) LMNAALDH1A1CYP3A4HSD17B10CHKA
Hydrochloric Acid SCHEMBL9330763 0.82 MEN1 (0.39) LMNAALDH1A1CYP3A4HSD17B10CHKA
Bromide SCHEMBL9328651 0.82 CHRM2 (0.42) LMNAALDH1A1CYP3A4HSD17B10CHKA
Iodide SCHEMBL5455905 0.82 HTT (0.53) LMNAALDH1A1CYP3A4HSD17B10HTT

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 68 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0253837-B1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS MALLINCKRODT SPECIALTY CHEMICALS COMPANY (US) 1991-10-09 EP claimed
US-4927980-A REACTING CHLOROAROMATIC COMPOUND WITH ALKALI METAL FLUORIDE SALTS MALLINCKRODT INC. (US) 1990-05-22 US claimed
EP-0253837-A4 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS. MALLINCKRODT INC (US) 1988-04-26 EP claimed
EP-0253837-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS. MALLINCKRODT INC (US) 1988-01-27 EP claimed
WO-1987004148-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS MALLINCKRODT, INC. (US) 1987-07-16 WO claimed
US-10676571-B2 Polyetherimides with improved melt stability SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2020-06-09 US disclosed
EP-2904033-B1 POLYETHERIMIDE COMPOSITIONS, METHODS OF MANUFACTURE, AND ARTICLES FORMED THEREFROM SABIC GLOBAL TECHNOLOGIES BV (NL) 2019-05-22 EP disclosed
EP-2904032-B1 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC GLOBAL TECHNOLOGIES BV (NL) 2018-03-07 EP disclosed
EP-3077445-A1 POLYETHERIMIDES WITH IMPROVED MELT STABILITY SABIC Global Technologies B.V. (NL) 2016-10-12 EP disclosed
US-9127127-B2 Polyetherimide compositions, methods of manufacture, and articles formed therefrom SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2015-09-08 US disclosed
EP-2904033-A1 POLYETHERIMIDE COMPOSITIONS, METHODS OF MANUFACTURE, AND ARTICLES FORMED THEREFROM SABIC Global Technologies B.V. (NL) 2015-08-12 EP disclosed
EP-2904032-A2 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC Global Technologies B.V. (NL) 2015-08-12 EP disclosed
EP-0253837-A4 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS. MALLINCKRODT INC (US) 1988-04-26 EP disclosed
EP-0253836-A1 PREPARATION OF FLUOROAROMATIC COMPOUNDS IN DISPERSION OF POTASSIUM FLUORIDE. MALLINCKRODT INC (US) 1988-01-27 EP disclosed
EP-0253837-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS. MALLINCKRODT INC (US) 1988-01-27 EP disclosed
EP-0253837-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS. MALLINCKRODT INC (US) 1988-01-27 EP disclosed
WO-1987004148-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS MALLINCKRODT, INC. (US) 1987-07-16 WO disclosed
WO-1987004148-A1 CATALYTIC METHOD FOR PRODUCING FLUOROAROMATIC COMPOUNDS USING BRANCHED ALKYL PYRIDINIUM SALTS MALLINCKRODT, INC. (US) 1987-07-16 WO disclosed
WO-1987004151-A1 PREPARATION OF FLUOROAROMATIC COMPOUNDS IN DISPERSION OF POTASSIUM FLUORIDE MALLINCKRODT, INC. (US) 1987-07-16 WO disclosed
US-4642398-A PHASE TRANSFER CATALYSIS MALLINCKRODT, INC. (US) 1987-02-10 US disclosed