Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7108463

CCCC[S+](CCCC)Cc1ccc(Br)cc1.[Cl-]

nearest known ligand 0.43

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
SLC6A2 known ✓ P23975 2/20 0.33
SLC6A3 known ✓ Q01959 2/20 0.33
CHRM2 known ✓ P08172 1/20 0.33
CHRM1 known ✓ P11229 1/20 0.33
CHRM3 known ✓ P20309 1/20 0.33
ACHE known ✓ P22303 1/20 0.33
CYP1A2 P05177 2/20 0.43
CYP2D6 P10635 2/20 0.43
CYP2C19 P33261 2/20 0.43
LMNA P02545 2/20 0.42
NPC1 O15118 2/20 0.39
NFKB1 P19838 2/20 0.39
RAB9A P51151 2/20 0.39
NFKB2 Q00653 2/20 0.39
RELA Q04206 2/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
MAPK1 P28482 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
GAA P10253 1/20 0.35
TAAR1 Q96RJ0 3/20 0.34

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
SCHEMBL7106497 0.98 CYP1A2 (0.44) CYP1A2CYP2D6CYP2C19LMNANPC1
Hydrochloric Acid SCHEMBL8730207 0.80 TP53 (0.42) SMN1; SMN2MAPK1L3MBTL1TP53
SCHEMBL8757226 0.80 SIGMAR1 (0.34) CYP1A2CYP2D6CYP2C19LMNANPC1
Hydrochloric Acid SCHEMBL392362 0.79 ESR1 (0.58) LMNAESR1ADRA2AADORA3TACR2
SCHEMBL4237394 0.78 TP53 (0.42) SMN1; SMN2MAPK1TP53
Hydrochloric Acid SCHEMBL391947 0.77 LMNA (0.46) CYP1A2CYP2D6CYP2C19LMNANPC1
Hydrochloric Acid SCHEMBL9343453 0.76 MEN1 (0.46) SMN1; SMN2MAPK1TP53
SCHEMBL9120855 0.74 TP53 (0.42) SMN1; SMN2MAPK1TP53
Water SCHEMBL9247303 0.72 DNM1 (0.43) SMN1; SMN2MAPK1TP53
SCHEMBL8757335 0.71 DNM1 (0.46) SMN1; SMN2MAPK1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0974595-B1 PROCESS FOR PRODUCING BORON COMPOUNDS SHOWA DENKO KK (JP) 2003-10-01 EP disclosed
EP-0922708-B1 Production method of borate compounds SHOWA DENKO KK (JP) 2003-05-14 EP disclosed
US-6140537-A REACTING AN ORGANIC OXYBORON COMPOUND WITH LITHIUM, MAGNESIUM, OR COMPOUND THEREOF; FORMING BORON ANION COMPOUND; ION EXCHANGING SHOWA DENKO K.K. (JP) 2000-10-31 US disclosed
EP-0974595-A1 PROCESS FOR PRODUCING BORON COMPOUNDS Showa Denko Kabushiki Kaisha (JP) 2000-01-26 EP disclosed
US-6002044-A REACTING A LITHIUM OR MAGNEISIUM, A HALIDE AND A BORONATE PRECURSOR OBTAINED IN A FIRSST SIMILAR STEP USING A BORIDE; ADDING AN ONIIUM HALIDE TO THE METAL BORATE; PURITY SHOWA DENKO K.K. (JP) 1999-12-14 US disclosed
EP-0922708-A2 Production method of borate compounds SHOWA DENKO KABUSHIKI KAISHA (JP) 1999-06-16 EP disclosed