Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1070025

CC(C)(C)C1=C([Cr+2])c2ccccc2C1c1cccc2cccnc12.[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 0.35
LMNA P02545 3/20 0.40
CCR1 P32246 3/20 0.40
CCR5 P51681 3/20 0.40
CCR8 P51685 3/20 0.40
KDM4E B2RXH2 3/20 0.40
MAPT P10636 3/20 0.40
MMP2 P08253 2/20 0.40
TSHR P16473 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
TDP1 Q9NUW8 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

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 SCHEMBL1071469 0.82 SMN1; SMN2 (0.43) LMNACCR1CCR5CCR8KDM4E
SCHEMBL28517555 0.79 KDM4E (0.54) LMNACCR1CCR5CCR8KDM4E
Hydrochloric Acid SCHEMBL1072267 0.78 CCR1 (0.40) LMNACCR1CCR5CCR8KDM4E
Hydrochloric Acid SCHEMBL1071824 0.78 MAPT (0.40) LMNACCR1CCR5CCR8KDM4E
Hydrochloric Acid SCHEMBL819577 0.77 KDM4E (0.41) LMNACCR1CCR5CCR8KDM4E
Hydrochloric Acid SCHEMBL5009057 0.74 P2RX7 (0.40) LMNACCR1CCR5CCR8KDM4E
SCHEMBL27587384 0.72 LMNA (0.39) LMNACCR1CCR5CCR8KDM4E
SCHEMBL7546290 0.70 MAPK1 (0.37) LMNACCR1CCR5CCR8KDM4E
SCHEMBL6131342 0.69 CCR1 (0.39) LMNACCR1CCR5CCR8KDM4E
Hydrochloric Acid SCHEMBL1069659 0.68 CCR1 (0.40) LMNACCR1CCR5CCR8KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7618912-B2 Preparation of supported catalyst systems BASELL POLYOLEFINE GMBH (DE) 2009-11-17 US claimed
US-20060166813-A1 Preparation of supported catalyst systems BASELL POLYOLEFINE GMBH (DE) 2006-07-27 US claimed
EP-1824888-B1 MONOCYCLOPENTADIENYL COMPLEXES BASELL POLYOLEFINE GMBH (DE) 2017-01-18 EP disclosed
EP-1740626-B1 CATALYST SYSTEM FOR OLEFIN POLYMERIZATION, ITS PRODUCTION AND USE BASELL POLYOLEFINE GMBH (DE) 2014-10-22 EP disclosed
US-7973114-B2 Monocyclopentadienyl complexes BASELL POLYOLEFINE GMBH (DE) 2011-07-05 US disclosed
EP-1861409-B1 MONOCYCLOPENTADIENYL COMPLEXES BASELL POLYOLEFINE GMBH (DE) 2011-01-19 EP disclosed
US-7834107-B2 Preparation of polyolefins having high molecular weights in the presence of an organic transition metal compound in a gas-phase fluidized-bed reactor BASELL POLYOLEFINE GMBH (DE) 2010-11-16 US disclosed
US-7834112-B2 Method of polymerization of olefins BASELL POLYOLEFINE GMBH (DE) 2010-11-16 US disclosed
US-7795167-B2 Cyclopentadienyl complexes of group 6 substituted by silyl halides BASELL POLYOLEFINE GMBH (DE) 2010-09-14 US disclosed
US-7776980-B2 Monocyclopentadienyl complexes BASELL POLYOLEFINE GMBH (DE) 2010-08-17 US disclosed
EP-1572359-B1 MONOCYCLOPENTADIENYL COMPLEXES BASELL POLYOLEFINE GMBH (DE) 2010-04-28 EP disclosed
US-20040249095-A1 Method of polymerization of olefins BASELL POLYOLEFINE GMBH (DE) 2004-12-09 US disclosed
US-20040242880-A1 Monocyclopentadienyl complexes comprising a condensed heterocycle BASELL POLYOLEFINE GMBH (DE) 2004-12-02 US disclosed
US-6787498-B2 AS CATALYSTS FOR POLYMERIZATION OF OLEFINS BASELL POLYOLEFINE GMBH (DE) 2004-09-07 US disclosed
US-6699948-B2 AS CATALYSTS FOR POLYMERIZATION OF OLEFINS BASF AKTIENGESELLSCHAFT (DE) 2004-03-02 US disclosed
US-20040033890-A1 Catalyst system for carrying out olefin polymerization comprising a calcined hydro-talcite serving as a supporting material LYONDELL CHEMICAL TECHNOLOGY, L.P. 2004-02-19 US disclosed
US-20030176275-A1 Catalytic solid supported on calcined hydrotalcite for olefinic polymerisation BASELL POLYOLEFINE GMBH (DE) 2003-09-18 US disclosed
US-20030036662-A1 Monocyclopentadienyl complexes of chromium, molybdenum or tungsten MIHAN SHAHRAM (DE) 2003-02-20 US disclosed
US-20030036658-A1 Monocyclopentadienyl complexes of chromium, molybdenum or tungsten MIHAN SHAHRAM (DE) 2003-02-20 US disclosed
US-6437161-B1 OLEFIN POLYMERIZATION CATALYSTS; SUBSTITUENT ON THE CYCLOPENTADIENYL RING CARRIES A DONOR FUNCTION WHICH IS BONDED RIGIDLY, NOT EXCLUSIVELY VIA SP3-HYBRIDIZED CARBON OR SILICON ATOMS, BASF AKTIENGESELLSCHAFT (DE) 2002-08-20 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 (3 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-20040242880-A1 Monocyclopentadienyl complexes comprising a condensed heterocycle MCM4, MCM3, CCNC CHRM1 2515/4885LMNA 3277/4885CCR1 1453/4885
US-20030036662-A1 Monocyclopentadienyl complexes of chromium, molybdenum or tungsten SKIC3, ORC3, MCM3 CHRM1 1028/4885LMNA 3742/4885CCR1 180/4885
US-20030036658-A1 Monocyclopentadienyl complexes of chromium, molybdenum or tungsten SKIC3, ORC3, MCM3 CHRM1 1028/4885LMNA 3742/4885CCR1 180/4885

“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.