Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6574072

CCCCCCCCCCCCCCCC[N+](C)(C)Cc1ccccc1CC.[Cl-]

nearest known ligand 0.65

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
CHRM2 known ✓ P08172 1/20 0.47
CHRM1 known ✓ P11229 1/20 0.47
CHRM3 known ✓ P20309 1/20 0.47
SLC6A2 known ✓ P23975 1/20 0.47
SLC6A3 known ✓ Q01959 1/20 0.47
KMT2A Q03164 3/20 0.65
MEN1 O00255 2/20 0.65
MAPK1 P28482 2/20 0.65
SMN1; SMN2 Q16637 2/20 0.65
TP53 P04637 1/20 0.65
HTT P42858 5/20 0.63
DNM1 Q05193 7/20 0.62
HSP90AA1 P07900 2/20 0.53
RAD52 P43351 2/20 0.53
PSMD14 O00487 1/20 0.53
MMP2 P08253 1/20 0.53
MC4R P32245 1/20 0.53
MLNR O43193 1/20 0.47
NR1I2 O75469 1/20 0.47
ESR1 P03372 1/20 0.47

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 SCHEMBL6574708 1.00 KMT2A (0.65) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL1876836 1.00 KMT2A (0.65) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL6576259 1.00 KMT2A (0.65) KMT2AMEN1MAPK1SMN1; SMN2TP53
SCHEMBL6574075 0.98 DNM1 (0.64) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL7764453 0.95 KMT2A (0.71) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL7760973 0.95 KMT2A (0.71) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL8720796 0.95 KMT2A (0.71) KMT2AMEN1MAPK1SMN1; SMN2TP53
Hydrochloric Acid SCHEMBL11010357 0.92 MEN1 (0.79) KMT2AMEN1MAPK1SMN1; SMN2TP53
Sulfuric Acid SCHEMBL7765908 0.87 DNM1 (0.58) KMT2AMEN1MAPK1SMN1; SMN2TP53
Acetic Acid SCHEMBL7764531 0.87 DNM1 (0.63) KMT2AMEN1MAPK1SMN1; SMN2TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0764676-B1 Method of preparing polycarbonate-polysiloxane block copolymers GEN ELECTRIC (US) 2004-04-28 EP claimed
EP-0764676-B1 Method of preparing polycarbonate-polysiloxane block copolymers GEN ELECTRIC (US) 2004-04-28 EP disclosed
US-5616674-A USING PHASE TRANSFER CATALYSTS GENERAL ELECTRIC COMPANY (US) 1997-04-01 US disclosed
EP-0764676-A2 Method of preparing polycarbonate-polysiloxane block copolymers GENERAL ELECTRIC COMPANY (US) 1997-03-26 EP disclosed
US-4761507-A Isomerization of linalyl halides with quaternary salts UNION CAMP CORPORATION (US) 1988-08-02 US disclosed
EP-0132544-B1 HYDROHALOGENATION OF CONJUGATED DIENES Union Camp Corporation (US) 1987-11-04 EP disclosed
EP-0132543-B1 ISOMERIZATION OF ALLYLIC HALIDES WITH QUATERNARY SALTS Union Camp Corporation (US) 1986-10-08 EP disclosed
EP-0132543-A1 Isomerization of allylic halides with quaternary salts Union Camp Corporation (US) 1985-02-13 EP disclosed
EP-0132544-A1 Hydrohalogenation of conjugated dienes Union Camp Corporation (US) 1985-02-13 EP disclosed