Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9491983

C(=Cc1cccc(Oc2ccccc2)c1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-]

nearest known ligand 0.52

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
▸ EPOR P19235 7/20 0.52
▸ ALOX5 P09917 3/20 0.50
▸ PTGS1 P23219 2/20 0.50
▸ PTGS2 P35354 2/20 0.50
▸ ALOX5AP P20292 1/20 0.50
▸ TLR4 O00206 1/20 0.48
▸ TLR2 O60603 1/20 0.48
▸ PPARG P37231 1/20 0.47
▸ GRIK1 P39086 1/20 0.41
▸ GRIK2 Q13002 1/20 0.41
▸ KDM5A P29375 1/20 0.40
▸ BACE1 P56817 1/20 0.40
▸ MEN1 O00255 1/20 0.40
▸ NPC1 O15118 1/20 0.40
▸ POLB P06746 1/20 0.40
▸ RAB9A P51151 1/20 0.40
▸ KMT2A Q03164 1/20 0.40
▸ LCK P06239 1/20 0.38
▸ LMNA P02545 1/20 0.38
▸ MAPT P10636 1/20 0.38

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 SCHEMBL9493233 1.00 EPOR (0.52) EPORALOX5PTGS1PTGS2ALOX5AP
Hydrochloric Acid SCHEMBL9492580 0.92 EPOR (0.46) EPORALOX5PTGS1PTGS2ALOX5AP
Hydrochloric Acid SCHEMBL9493052 0.92 EPOR (0.46) EPORALOX5PTGS1PTGS2ALOX5AP
Hydrochloric Acid SCHEMBL10446299 0.92 EPOR (0.46) EPORALOX5PTGS1PTGS2ALOX5AP
Hydrochloric Acid SCHEMBL2452749 0.81 HTR2A (0.50) GRIK1GRIK2
Hydrochloric Acid SCHEMBL2452746 0.81 HTR2A (0.50) GRIK1GRIK2
Hydrochloric Acid SCHEMBL9493793 0.80 TTR (0.35) EPORALOX5PTGS1PTGS2ALOX5AP
Hydrochloric Acid SCHEMBL9493796 0.80 TTR (0.35) EPORALOX5PTGS1PTGS2ALOX5AP
Water SCHEMBL8528185 0.77 HTR2A (0.50) GRIK1GRIK2
Bromide SCHEMBL2449964 0.77 HTR2A (0.50) GRIK1GRIK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0279531-B1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF INSECTICIDALLY ACTIVE COMPOUNDS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-03-10 — — EP claimed
EP-0279531-A2 Process and intermediates for the preparation of insecticidally active compounds IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-08-24 — — EP claimed
EP-0279531-B1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF INSECTICIDALLY ACTIVE COMPOUNDS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-03-10 — — EP disclosed
US-5081273-A PROCESS FOR THE PREPARATION OF INSECTICIDALLY ACTIVE DIPHENYL ETHER COMPOUNDS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-01-14 — — US disclosed
EP-0240121-B1 DIPHENYL ETHER DERIVATIVES IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-04-17 — — EP disclosed
EP-0390228-A2 Chemical intermediates IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-10-03 — — EP disclosed
US-4942264-A WITTIG REACTION FOLLOWED BY REDUCTION IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-07-17 — — US disclosed
US-4791139-A Diphenyl ether derivatives and their use as insecticides IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-12-13 — — US disclosed
EP-0279531-A2 Process and intermediates for the preparation of insecticidally active compounds IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-08-24 — — EP disclosed
EP-0240121-A2 Diphenyl ether derivatives IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1987-10-07 — — EP disclosed
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