Hydrochloric Acid

Hydrochloric Acid

SCHEMBL814062

Cc1cccc(C)c1NCCNCCNc1c(C(C)C)cccc1C(C)C.[Cl-].[Cl-].[Co+2]

nearest known ligand 0.43

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
SLC6A2 known ✓ P23975 1/20 0.33
MAPK1 P28482 1/20 0.43
NLRP3 Q96P20 2/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
KMT2A Q03164 4/20 0.39
MEN1 O00255 3/20 0.39
L3MBTL1 Q9Y468 1/20 0.37
LMNA P02545 5/20 0.35
MAPT P10636 1/20 0.35
HTT P42858 1/20 0.35
GABRA1 P14867 2/20 0.34
GABRG2 P18507 2/20 0.34
GABRB3 P28472 2/20 0.34
HTR1A P08908 1/20 0.34
ADRA1D P25100 1/20 0.34
ADRA1A P35348 1/20 0.34
ADRA1B P35368 1/20 0.34
ALOX12 P18054 1/20 0.34
RECQL P46063 1/20 0.34
RAB9A P51151 1/20 0.34

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 SCHEMBL813566 0.97 MAPK1 (0.43) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL813075 0.92 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL814290 0.89 MAPK1 (0.35) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL813206 0.89 SMN1; SMN2 (0.38) MAPK1NLRP3SMN1; SMN2KMT2ALMNA
Hydrochloric Acid SCHEMBL814339 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL814535 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL814002 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL814490 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL813347 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL813947 0.88 SMN1; SMN2 (0.46) MAPK1NLRP3SMN1; SMN2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8058372-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2011-11-15 US disclosed
US-20080319147-A1 Catalyst Composition II EXXONMOBIL CHEMICAL PATENTS INC. 2008-12-25 US disclosed
US-7371803-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2008-05-13 US disclosed
US-20070066776-A1 Catalyst composition II SOLAN GREGORY A 2007-03-22 US disclosed
US-7189791-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2007-03-13 US disclosed
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 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-20040266961-A1 Catalyst composition II MLX, CBX2, BMX SLC6A2 2736/4885MAPK1 4372/4885NLRP3 919/4885

“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.