Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2653092

CCCCP(=O)(c1ccccc1)c1ccccc1.CCCCP(=O)(c1ccccc1)c1ccccc1.[Cl-].[Cl-].[Pd+2]

nearest known ligand 0.67

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 16)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 3/20 0.67
GAA P10253 2/20 0.67
MAPT P10636 2/20 0.67
ALDH1A1 P00352 2/20 0.67
ALPG P10696 1/20 0.67
ALOX12 P18054 1/20 0.67
NPY1R P25929 1/20 0.67
HTT P42858 1/20 0.67
NPY2R P49146 1/20 0.67
L3MBTL1 Q9Y468 1/20 0.61
KMT2A Q03164 3/20 0.56
MEN1 O00255 2/20 0.56
POLB P06746 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
TSHR P16473 1/20 0.45
USP2 O75604 1/20 0.45

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 SCHEMBL9419776 1.00 NPSR1 (0.67) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL780075 0.96 NPSR1 (0.72) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL8548131 0.94 NPSR1 (0.69) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL1727341 0.90 NPSR1 (0.76) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL6767391 0.88 NPSR1 (0.80) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL10404685 0.88 NPSR1 (0.80) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL1724978 0.88 NPSR1 (0.80) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL1726010 0.88 NPSR1 (0.80) NPSR1GAAMAPTALDH1A1ALPG
Propane SCHEMBL29000300 0.88 NPSR1 (0.73) NPSR1GAAMAPTALDH1A1ALPG
SCHEMBL10985692 0.88 NPSR1 (0.80) NPSR1GAAMAPTALDH1A1ALPG

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
EP-1532120-B1 PHENYLPYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS MERCK SHARP & DOHME (GB) 2009-01-14 EP disclosed
US-20060235021-A1 Phenylpyridazine derivatives as ligands for gaba receptors MERCK SHARP & DOHME LTD. (GB) 2006-10-19 US disclosed
EP-1532120-A1 PHENYLPYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS MERCK SHARP & DOHME LTD. (GB) 2005-05-25 EP disclosed
WO-2004014865-A1 PHENYLPYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS MERCK SHARP & DOHME LIMITED (GB) 2004-02-19 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060235021-A1 Phenylpyridazine derivatives as ligands for gaba receptors GABRA5, GABRA2, GABRA3 NPSR1 179/4885GAA 2683/4885MAPT 884/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.