Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7196439

COc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)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 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.47
ATM Q13315 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
LTA4H P09960 1/20 0.46
SLC6A4 P31645 1/20 0.43
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41
LDHA P00338 1/20 0.41
HTT P42858 1/20 0.40
IDO1 P14902 1/20 0.40
SIGMAR1 Q99720 1/20 0.39
LMNA P02545 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
PPARG P37231 1/20 0.39
PPARA Q07869 1/20 0.39
KDM4E B2RXH2 1/20 0.39
ALDH1A1 P00352 1/20 0.39
MAPT P10636 1/20 0.39
ALOX15 P16050 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
Iodide SCHEMBL7200711 0.97 L3MBTL1 (0.47) L3MBTL1ATMTDP1LTA4HSLC6A4
Bromide SCHEMBL7195760 0.97 L3MBTL1 (0.47) L3MBTL1ATMTDP1LTA4HSLC6A4
Acetic Acid SCHEMBL8750048 0.88 L3MBTL1 (0.50) L3MBTL1ATMTDP1LTA4HLDHA
Acetic Acid SCHEMBL7198886 0.86 TDP1 (0.48) L3MBTL1ATMTDP1LTA4HLDHA
Succinic Acid SCHEMBL7198874 0.86 L3MBTL1 (0.48) L3MBTL1ATMTDP1LDHALMNA
Hydrochloric Acid SCHEMBL7195761 0.83 TAAR1 (0.51) IDO1SIGMAR1MAPTSCN8A
Hydrochloric Acid SCHEMBL7200797 0.82 CYP19A1 (0.36) CYP1A2CYP2C19HTTIDO1LMNA
Hydrochloric Acid SCHEMBL6060719 0.82 TAAR1 (0.39) L3MBTL1TDP1SLC6A4CYP2D6SIGMAR1
Iodide SCHEMBL7197231 0.80 TAAR1 (0.51) IDO1SIGMAR1MAPTSCN8A
Bromide SCHEMBL7197342 0.80 TAAR1 (0.51) IDO1SIGMAR1MAPTSCN8A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed