Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7644423

C[Ti+2](C)(NC(=O)C1CCCCC1)C1C=C(c2ccccc2)c2ccccc21.[Cl-].[Cl-].[SiH4]

nearest known ligand 0.41

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 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.41
ADORA1 P30542 5/20 0.40
HPGD P15428 1/20 0.39
ADORA2A P29274 3/20 0.39
ADORA3 P0DMS8 3/20 0.39
CYP2C19 P33261 1/20 0.38
SMN1; SMN2 Q16637 2/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
LMNA P02545 1/20 0.38
NPSR1 Q6W5P4 1/20 0.38
CCKAR P32238 1/20 0.37
CCKBR P32239 1/20 0.37
HDAC1 Q13547 1/20 0.36
HDAC2 Q92769 1/20 0.36

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 SCHEMBL7753150 0.78 CYP2C19 (0.45) ALDH1A1HPGDCYP2C19SMN1; SMN2MEN1
Hydrochloric Acid SCHEMBL7630764 0.74 CYP2C19 (0.40) ALDH1A1HPGDCYP2C19SMN1; SMN2KMT2A
SCHEMBL7644429 0.70 ALDH1A1 (0.40) ALDH1A1ADORA1HPGDADORA2AADORA3
Hydrochloric Acid SCHEMBL7752408 0.66 CYP2C19 (0.45) ALDH1A1HPGDCYP2C19SMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL5968682 0.65 HPGD (0.33) ALDH1A1ADORA1HPGDCYP2C19SMN1; SMN2
Hydrochloric Acid SCHEMBL7753199 0.64 CYP2C19 (0.45) ALDH1A1HPGDCYP2C19SMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL5854814 0.62 CYP2C19 (0.43) ALDH1A1HPGDADORA3CYP2C19SMN1; SMN2
Hydrochloric Acid SCHEMBL5853853 0.62 CYP2C19 (0.43) ALDH1A1HPGDADORA3CYP2C19SMN1; SMN2
SCHEMBL38659461 0.62 ALDH1A1 (0.94) ALDH1A1ADORA1HPGDADORA2AADORA3
SCHEMBL17866226 0.61 CYP2C19 (0.45) ALDH1A1HPGDCYP2C19SMN1; SMN2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0946574-B1 3-ARYL SUBSTITUTED INDENYL CONTAINING METAL COMPLEXES AND POLYMERIZATION PROCESS DOW CHEMICAL CO (US) 2002-02-13 EP claimed
US-5866704-A 3-aryl substituted indenyl containing metal complexes and polymerization process THE DOW CHEMICAL COMPANY (US) 1999-02-02 US claimed