Hydrochloric Acid

Hydrochloric Acid

SCHEMBL815303

Cc1cc(C)c(NCCN(C)CCNc2c(C)cccc2C)c(C)c1.[Cl-].[Cl-].[Co+2]

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 10)

geneUniProtsupporting neighboursconfidence
RAPGEF4 Q8WZA2 10/20 0.40
GAA P10253 1/20 0.37
CYP3A4 P08684 2/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2D6 P10635 1/20 0.33
MAPT P10636 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
HTT P42858 1/20 0.33
CRHR1 P34998 5/20 0.33

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 SCHEMBL814981 0.97 RAPGEF4 (0.40) RAPGEF4GAACYP3A4CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL813576 0.92 RAPGEF4 (0.41) RAPGEF4GAACYP3A4MAPTHTT
Hydrochloric Acid SCHEMBL813091 0.92 MAPT (0.36) GAACYP3A4CYP1A2MAPTCYP2C9
Hydrochloric Acid SCHEMBL815569 0.90 RAPGEF4 (0.43) RAPGEF4GAACYP3A4MAPTHTT
Hydrochloric Acid SCHEMBL814976 0.90 MAPT (0.38) GAACYP3A4CYP1A2MAPTCYP2C9
Hydrochloric Acid SCHEMBL814712 0.88 MAPT (0.36) GAACYP3A4CYP1A2MAPTCYP2C9
Hydrochloric Acid SCHEMBL814448 0.88 RAPGEF4 (0.41) RAPGEF4GAACYP3A4MAPTHTT
Hydrochloric Acid SCHEMBL815004 0.88 RAPGEF4 (0.41) RAPGEF4GAACYP3A4MAPTHTT
Hydrochloric Acid SCHEMBL814370 0.88 MAPT (0.36) GAACYP3A4CYP1A2MAPTCYP2C9
Hydrochloric Acid SCHEMBL813022 0.88 MAPT (0.36) GAACYP3A4CYP1A2MAPTCYP2C9

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 8 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
EP-1641842-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND Exxonmobil Chemical Patents Inc. (US) 2006-04-05 EP disclosed
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 US disclosed
WO-2004106390-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND EXXONMOBIL CHEMICAL PATENTS INC. (US) 2004-12-09 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-20040266961-A1 Catalyst composition II MLX, CBX2, BMX RAPGEF4 4437/4885GAA 3583/4885CYP3A4 2959/4885

“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.