Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5000248

Clc1ccc(CC2=CCC(c3cccc4cccnc34)=C2[Cr+2])cc1.[Cl-].[Cl-]

nearest known ligand 0.40

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
LMNA P02545 4/20 0.40
SMN1; SMN2 Q16637 3/20 0.40
GAA P10253 2/20 0.40
L3MBTL1 Q9Y468 2/20 0.40
KMT2A Q03164 3/20 0.39
EGLN1 Q9GZT9 2/20 0.37
MAPT P10636 2/20 0.37
HTT P42858 2/20 0.37
ALDH1A1 P00352 2/20 0.37
HPGD P15428 1/20 0.37
POLB P06746 1/20 0.36
KDM4E B2RXH2 2/20 0.36
P2RX7 Q99572 1/20 0.36
SLC40A1 Q9NP59 1/20 0.35
KDR P35968 1/20 0.35
MEN1 O00255 1/20 0.35
NPSR1 Q6W5P4 1/20 0.35
GMNN O75496 1/20 0.35
TP53 P04637 1/20 0.35
HSP90AA1 P07900 1/20 0.35

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 SCHEMBL819123 0.79 LMNA (0.38) LMNASMN1; SMN2GAAL3MBTL1KMT2A
Hydrochloric Acid SCHEMBL5009094 0.79 MAPT (0.38) LMNASMN1; SMN2L3MBTL1KMT2AMAPT
Hydrochloric Acid SCHEMBL820651 0.69 LMNA (0.41) LMNASMN1; SMN2L3MBTL1KMT2AMAPT
Hydrochloric Acid SCHEMBL819882 0.69 KDM4E (0.40) LMNASMN1; SMN2GAAL3MBTL1KMT2A
Hydrochloric Acid SCHEMBL3086287 0.69 CCR1 (0.40) LMNASMN1; SMN2GAAL3MBTL1KMT2A
SCHEMBL16581166 0.68 MMP2 (0.54) LMNASMN1; SMN2GAAL3MBTL1KMT2A
Hydrochloric Acid SCHEMBL5000247 0.68 LMNA (0.39) LMNASMN1; SMN2GAAL3MBTL1KMT2A
Hydrochloric Acid SCHEMBL819935 0.66 CCR1 (0.37) LMNASMN1; SMN2GAAL3MBTL1KMT2A
SCHEMBL6131338 0.66 CCR1 (0.46) LMNASMN1; SMN2L3MBTL1MAPTHTT
Hydrochloric Acid SCHEMBL5006801 0.64 P2RX7 (0.45) LMNASMN1; SMN2L3MBTL1KMT2AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080269445-A1 Monocyclopentadienyl Complexes BASELL POLYOLEFINE GMBH (DE) 2008-10-30 US 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-20080269445-A1 Monocyclopentadienyl Complexes PCBP1, COASY, PORCN LMNA 2672/4885SMN1; SMN2 3981/4885GAA 4642/4885

“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.