Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9549734

CCN(CC)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-]

nearest known ligand 0.61

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
▸ CHRM1 known ✓ P11229 2/20 0.46
▸ SLC6A2 known ✓ P23975 2/20 0.46
▸ SLC6A3 known ✓ Q01959 2/20 0.46
▸ CHRM2 known ✓ P08172 1/20 0.46
▸ SIGMAR1 Q99720 2/20 0.61
▸ HIF1A Q16665 1/20 0.48
▸ KCNH2 Q12809 4/20 0.46
▸ SLC6A4 P31645 2/20 0.46
▸ ADRA1A P35348 2/20 0.46
▸ OPRM1 P35372 2/20 0.46
▸ DRD3 P35462 2/20 0.46
▸ HTR1A P08908 1/20 0.46
▸ ADRA2A P08913 1/20 0.46
▸ DRD1 P21728 1/20 0.46
▸ CACNA2D1 P54289 9/20 0.43
▸ ALDH1A1 P00352 1/20 0.41
▸ LMNA P02545 1/20 0.41
▸ CYP1A2 P05177 1/20 0.41
▸ CYP2D6 P10635 1/20 0.41
▸ MAPT P10636 1/20 0.40

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
Bromide SCHEMBL9549787 0.96 SIGMAR1 (0.61) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Bromide SCHEMBL9851216 0.91 SIGMAR1 (0.58) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Phosphoric Acid SCHEMBL9549735 0.90 SIGMAR1 (0.54) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Bromide SCHEMBL9239994 0.89 SIGMAR1 (0.56) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Acetic Acid SCHEMBL9549728 0.88 SIGMAR1 (0.51) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Acetic Acid SCHEMBL9848338 0.86 SIGMAR1 (0.50) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
SCHEMBL8536686 0.83 SIGMAR1 (0.56) SIGMAR1HIF1AKCNH2CHRM1SLC6A2
Hydrochloric Acid SCHEMBL9549516 0.81 HTR2A (0.53) SIGMAR1HIF1ASLC6A2SLC6A4CHRM2
Hydrochloric Acid SCHEMBL6060715 0.80 HIF1A (0.74) HIF1AALDH1A1CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL5091467 0.79 HIF1A (0.58) HIF1AALDH1A1CYP1A2CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5208317-A Molding materials of cured epoxy resins THE DOW CHEMICAL COMPANY (US) 1993-05-04 — — US disclosed
US-5109099-A ADVANCING EPOXY RESINS IN PRESENCE OF AMINO GROUP-CONTAINING PHOSPHONIUM CATALYST THE DOW CHEMICAL COMPANY (US) 1992-04-28 — — US disclosed
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
US-4981926-A Rapid and selective curing using phosphonium catalyst containing an amine group; polyepoxides THE DOW CHEMICAL COMPANY (US) 1991-01-01 — — US disclosed
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