Hydrochloric Acid

Hydrochloric Acid

SCHEMBL146933

[Cl-].[Cl-].[Pd+2].c1ccc(P(CCCCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.41

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 6)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
KDM4E B2RXH2 1/20 0.33
GAA P10253 1/20 0.33
ESR1 P03372 3/20 0.32
ESR2 Q92731 3/20 0.32

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 SCHEMBL19946521 0.95 CYP3A4 (0.41) CYP3A4TDP1KDM4EGAAESR1
Bromide SCHEMBL986162 0.95 CYP3A4 (0.41) CYP3A4TDP1ESR1ESR2
Hydrochloric Acid SCHEMBL196879 0.95 CYP3A4 (0.41) CYP3A4TDP1KDM4EGAAESR1
Hydrochloric Acid SCHEMBL987207 0.95 CYP3A4 (0.41) CYP3A4TDP1KDM4EGAAESR1
SCHEMBL29179 0.95 CYP3A4 (0.45) CYP3A4TDP1KDM4EGAAESR1
SCHEMBL689027 0.92 TDP1 (0.43) CYP3A4TDP1KDM4EGAAESR1
SCHEMBL2920316 0.92 CYP3A4 (0.43) CYP3A4TDP1KDM4EGAAESR1
SCHEMBL28797563 0.92 CYP3A4 (0.43) CYP3A4TDP1KDM4EGAAESR1
Hydrochloric Acid SCHEMBL9322645 0.92 CYP3A4 (0.43) CYP3A4TDP1KDM4EGAAESR1
SCHEMBL30486913 0.92 CYP3A4 (0.43) CYP3A4TDP1KDM4EGAAESR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230331699-A1 PREPARATION METHOD FOR CDK4/6 INHIBITOR CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-10-19 US claimed
US-20230144449-A1 TERMINAL FUNCTIONAL SIDE CHAIN-SUBSTITUTED DIKETOPYRROLOPYRROLE (DPP)-BASED TERPOLYMER AND PREPARATION METHOD AND USE THEREOF BEIJING INSTITUTE OF GRAPHIC COMMUNICATION (CN) 2023-05-11 US claimed
EP-4159728-A1 PREPARATION METHOD FOR CDK4/6 INHIBITOR CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-04-05 EP claimed
WO-2021259203-A1 PREPARATION METHOD FOR CDK4/6 INHIBITOR 正大天晴药业集团股份有限公司 2021-12-30 WO claimed
WO-2021129082-A1 METHOD FOR SYNTHESIZING α-ACRYLIC ACID COMPOUND BY USING PALLADIUM TO CATALYZE CARBON DIOXIDE AND ALKYNE 华南理工大学 2021-07-01 WO claimed
EP-2272831-A1 Process for the preparation of arylpyridinyl compounds Prime European Therapeuticals S.p.A. (IT) 2011-01-12 EP claimed
US-20090124577-A1 Intermediate Compounds for the Preparation of an Angiotensin II Receptor Antagonist ENANTIA SI 2009-05-14 US claimed
EP-1384717-A2 Tetrazolylphenylboronic acid intermediates for the synthesis of A II receptor antagonists E.I. DUPONT DE NEMOURS AND COMPANY (US) 2004-01-28 EP claimed
EP-0914318-A1 PYRAZINES KINGS COLLEGE LONDON (GB) 1999-05-12 EP claimed
WO-1997043267-A1 PYRAZINES KINGS COLLEGE LONDON (GB) 1997-11-20 WO claimed
EP-0643704-A4 TETRAZOLYLPHENYLBORONIC ACID INTERMEDIATES FOR THE SYNTHESIS OF AII RECEPTOR ANTAGONISTS. 1995-04-12 EP claimed
EP-0643704-A1 TETRAZOLYLPHENYLBORONIC ACID INTERMEDIATES FOR THE SYNTHESIS OF AII RECEPTOR ANTAGONISTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1995-03-22 EP claimed
US-5310928-A Process for preparing biphenyltetrazole compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1994-05-10 US claimed
WO-1993010106-A1 TETRAZOLYLPHENYLBORONIC ACID INTERMEDIATES FOR THE SYNTHESIS OF AII RECEPTOR ANTAGONISTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-05-27 WO claimed
US-20260062412-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY CHUGAI PHARMACEUTICAL CO LTD (JP) 2026-03-05 US disclosed
EP-4647424-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-11-12 EP disclosed
EP-4087836-B1 PROCESSES FOR PREPARING TRIAZOLE GLYCOLATE OXIDASE INHIBITORS CANTERO THERAPEUTICS INC (US) 2025-10-08 EP disclosed
US-4831144-A 1H-pyrrolo [3,2-c]pyrrolidines protected in 1-position useful as intermediates SANOFI (FR) 1989-05-16 US disclosed
EP-0070185-B1 PREPARATION OF LOWER ALKYL 2-FORMYL-3-(6-METHYL-3-PYRIDINYL)-PROPIONATES SMITHKLINE BECKMAN CORPORATION (US) 1985-04-10 EP disclosed
EP-0070185-A1 Preparation of lower alkyl 2-formyl-3-(6-methyl-3-pyridinyl)-propionates SMITHKLINE BECKMAN CORPORATION (US) 1983-01-19 EP 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-20090124577-A1 Intermediate Compounds for the Preparation of an Angiotensin II Receptor Antagonist AGTR2, AGTR1, ACE CYP3A4 230/4885TDP1 4557/4885KDM4E 3293/4885
US-20230331699-A1 PREPARATION METHOD FOR CDK4/6 INHIBITOR CDK4, CDK6, CDK2 CYP3A4 968/4885TDP1 1083/4885KDM4E 381/4885
US-20260062412-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY MYT1, NTMT1, MYL6 CYP3A4 1957/4885TDP1 1883/4885KDM4E 191/4885

“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.