Hydrochloric Acid

Hydrochloric Acid

SCHEMBL820330

CC1=C(c2cccc3cccnc23)CC([Cr+2])=C1c1ccccc1.[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
CHRM1 known ✓ P11229 1/20 0.38
LMNA P02545 5/20 0.40
CCR1 P32246 4/20 0.40
CCR8 P51685 4/20 0.40
CCR5 P51681 3/20 0.40
MMP2 P08253 2/20 0.40
TSHR P16473 2/20 0.40
KDM4E B2RXH2 2/20 0.40
MAPT P10636 2/20 0.40
GMNN O75496 1/20 0.40
TP53 P04637 1/20 0.40
HSP90AA1 P07900 1/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2D6 P10635 1/20 0.40
MMP9 P14780 1/20 0.40
ALOX15 P16050 1/20 0.40
NFKB1 P19838 1/20 0.40
MMP8 P22894 1/20 0.40
THPO P40225 1/20 0.40
MTOR P42345 1/20 0.40

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 SCHEMBL819935 0.88 CCR1 (0.37) LMNACCR1CCR8CCR5MMP2
Hydrochloric Acid SCHEMBL819634 0.85 CCR1 (0.40) LMNACCR1CCR8CCR5MMP2
Hydrochloric Acid SCHEMBL1685890 0.85 TOP1 (0.43) LMNAMAPTHSP90AA1HTTSMN1; SMN2
Hydrochloric Acid SCHEMBL5006801 0.79 P2RX7 (0.45) LMNACCR1CCR8CCR5MMP2
Hydrochloric Acid SCHEMBL1072414 0.79 CCR1 (0.46) LMNACCR1CCR8CCR5MMP2
SCHEMBL3086250 0.77 KDM4E (0.47) LMNACCR1CCR8CCR5MMP2
SCHEMBL2875750 0.76 CCR1 (0.40) LMNACCR1CCR8CCR5MMP2
SCHEMBL27739271 0.75 CCR1 (0.38) LMNACCR1CCR8CCR5MMP2
Hydrochloric Acid SCHEMBL820651 0.74 LMNA (0.41) LMNACCR1CCR8CCR5MMP2
SCHEMBL4148271 0.74 MMP2 (0.60) LMNACCR1CCR8CCR5MMP2

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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1943281-B1 HYBRID CATALYST SYSTEMS SUPPORTED ON MAGNESIUM HALIDE BASELL POLYOLEFINE GMBH (DE) 2017-09-20 EP disclosed
EP-1740626-B1 CATALYST SYSTEM FOR OLEFIN POLYMERIZATION, ITS PRODUCTION AND USE BASELL POLYOLEFINE GMBH (DE) 2014-10-22 EP disclosed
US-8563674-B2 Polyethylene and catalyst composition for its preparation BASELL POLYOLEFINE GMBH (DE) 2013-10-22 US disclosed
US-20120010377-A1 Catalyst System for the Polymerization of Alpha-Olefins BASELL POLYOLEFINE GMBH (DE) 2012-01-12 US disclosed
US-7928051-B2 Polyethylene for injection moldings BASELL POLYOLEFINE GMBH (DE) 2011-04-19 US disclosed
US-7868108-B2 Transition metal compound, ligand system, catalyst system and process for preparing polyolefins BASELL POLYOLEFINE GMBH (DE) 2011-01-11 US disclosed
US-20100311925-A1 Polyethylene and catalyst composition for its preparation BASELL POLYOLEFINE GMBH (DE) 2010-12-09 US disclosed
US-7767613-B2 Polyethylene and catalyst composition for its preparation BASELL POLYOLEFINE GMBH (DE) 2010-08-03 US disclosed
US-7723448-B2 Hybrid catalyst systems supported on magnesium halide BASELL POLYOLEFINE GMBH (DE) 2010-05-25 US disclosed
EP-1753791-B1 POLYETHYLENE FOR INJECTION MOLDINGS BASELL POLYOLEFINE GMBH (DE) 2010-04-14 EP disclosed
EP-1753794-B8 POLYETHYLENE AND CATALYST COMPOSITION FOR ITS PREPARATION BASELL POLYOLEFINE GMBH (DE) 2008-07-16 EP disclosed
EP-1753794-B1 POLYETHYLENE AND CATALYST COMPOSITION FOR ITS PREPARATION BASELL POLYOLEFINE GMBH (DE) 2008-06-04 EP disclosed
US-20070255033-A1 Polyethylene for Injection Moldings BASELL POYOLEFINE GMBH (DE) 2007-11-01 US disclosed
US-20070213484-A1 Monocyclopentadienyl Complexes BASELL POLYOLEFINE GMBH (DE) 2007-09-13 US disclosed
US-20070213205-A1 Polyethylene and Catalyst Composition for its Preparation BASELL POLYOLEFINE GMBH (DE) 2007-09-13 US disclosed
US-20070207916-A1 Mixing organic transition metal compounds, hydrolyzed organoaluminum compound, and solvent, then impregnating dry porous support BASELL POLYOLEFINE GMBH (DE) 2007-09-06 US disclosed
EP-1753794-A1 POLYETHYLENE AND CATALYST COMPOSITION FOR ITS PREPARATION Basell Polyolefine GmbH (DE) 2007-02-21 EP disclosed
EP-1694689-A1 MONOCYCLOPENTADIENYL COMPLEXES Basell Polyolefine GmbH (DE) 2006-08-30 EP disclosed
WO-2005103100-A1 POLYETHYLENE AND CATALYST COMPOSITION FOR ITS PREPARATION BASELL POLYOLEFINE GMBH (DE) 2005-11-03 WO disclosed
WO-2005058928-A1 MONOCYCLOPENTADIENYL COMPLEXES BASELL POLYOLEFINE GMBH (DE) 2005-06-30 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-20070213484-A1 Monocyclopentadienyl Complexes PCBP1, COASY, PORCN CHRM1 2934/4885LMNA 2688/4885CCR1 1180/4885

“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.