Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5706254

COc1ccc(-c2c3nc(c(-c4ccc(OC)cc4)c4ccc([nH]4)c(-c4ccc(OC)cc4)c4nc(c(-c5ccc(OC)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1.[Cl-].[Cl-].[Cl-].[Fe+3]

nearest known ligand 0.54

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 19)

geneUniProtsupporting neighboursconfidence
▸ TERT O14746 4/20 0.54
▸ TOP1 P11387 4/20 0.54
▸ ABCG2 Q9UNQ0 1/20 0.53
▸ CYCS P99999 3/20 0.51
▸ ENPP2 Q13822 1/20 0.50
▸ KDM4E B2RXH2 1/20 0.43
▸ NPC1 O15118 1/20 0.43
▸ MAPT P10636 1/20 0.43
▸ CASP3 P42574 1/20 0.43
▸ RAB9A P51151 1/20 0.43
▸ SENP8 Q96LD8 1/20 0.43
▸ SENP7 Q9BQF6 1/20 0.43
▸ SENP6 Q9GZR1 1/20 0.43
▸ AURKA O14965 1/20 0.42
▸ CCNB2 O95067 1/20 0.42
▸ CDK1 P06493 1/20 0.42
▸ CCNB1 P14635 1/20 0.42
▸ RIPK1 Q13546 1/20 0.42
▸ CCNB3 Q8WWL7 1/20 0.42

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 SCHEMBL21111503 0.97 TERT (0.54) TERTTOP1ABCG2CYCSENPP2
Hydrochloric Acid SCHEMBL31122235 0.97 TERT (0.54) TERTTOP1ABCG2CYCSENPP2
SCHEMBL949511 0.97 TERT (0.57) TERTTOP1ABCG2CYCSENPP2
SCHEMBL29414382 0.97 TERT (0.57) TERTTOP1ABCG2CYCSENPP2
SCHEMBL2338257 0.95 TERT (0.55) TERTTOP1ABCG2CYCSENPP2
SCHEMBL20856304 0.95 TERT (0.59) TERTTOP1ABCG2CYCSENPP2
SCHEMBL22265228 0.95 TERT (0.55) TERTTOP1ABCG2CYCSENPP2
Hydrochloric Acid SCHEMBL15768782 0.95 TERT (0.55) TERTTOP1ABCG2CYCSENPP2
SCHEMBL8430292 0.95 TERT (0.55) TERTTOP1ABCG2CYCSENPP2
SCHEMBL29515314 0.95 TERT (0.55) TERTTOP1ABCG2CYCSENPP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11078302-B2 Polymerization methods NORTH CAROLINA STATE UNIVERSITY (US) 2021-08-03 — — US claimed
US-20190345269-A1 POLYMERIZATION METHODS NORTH CAROLINA STATE UNIVERSITY 2019-11-14 — — US claimed
CN-106290631-B A kind of method of pigment array sensing technology Fast Evaluation magma Quality of Liquors 江苏今世缘酒业股份有限公司 2018-11-27 — — CN claimed
CN-106290631-A A kind of method of pigment array sensing technology Fast Evaluation original plasm wine quality 江苏今世缘酒业股份有限公司 2017-01-04 — — CN claimed
US-20250270352-A1 METHODS OF REVERSIBLE-ADDITION FRAGMENTATION CHAIN TRANSFER STEP-GROWTH POLYMERIZATION AND POLYMERS THEREFROM NATIONAL SCIENCE FOUNDATION 2025-08-28 — — US disclosed
EP-2602655-B1 Ophthalmic filter ESSILOR INT (FR) 2024-04-03 — — EP disclosed
CN-117783019-A On-site detection method of CTC black tea production place based on solution phase color sensing array 安徽农业大学 2024-03-29 — — CN disclosed
US-11865521-B2 Bifunctional catalyst for hydrogenation of carbon dioxide, and method for preparing hydrocarbon by using same KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2024-01-09 — — US disclosed
US-11635547-B2 Composition for the manufacture of an ophthalmic lens comprising an encapsulated light-absorbing additive ESSILOR INTERNATIONAL (FR) 2023-04-25 — — US disclosed
EP-2602654-B1 Ophthalmic filter ESSILOR INT (FR) 2023-04-19 — — EP disclosed
EP-3497488-B2 OPHTALMIC LENS COMPRISING AN ENCAPSULATED LIGHT-ABSORBING ADDITIVE ESSILOR INT (FR) 2023-03-22 — — EP disclosed
WO-2023034335-A1 METHODS OF REVERSIBLE-ADDITION FRAGMENTATION CHAIN TRANSFER STEP-GROWTH POLYMERIZATION AND POLYMERS THEREFROM THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2023-03-09 — — WO disclosed
WO-2013084177-A1 OPHTHALMIC FILTER Essilor International (Compagnie Générale d'Optique) (FR) 2013-06-13 — — WO disclosed
WO-2013084178-A1 OPHTHALMIC FILTER Essilor International (Compagnie Générale d'Optique) (FR) 2013-06-13 — — WO disclosed
WO-2013084176-A1 METHOD OF DETERMINING THE CONFIGURATION OF AN OPHTHALMIC FILTER Essilor International (Compagnie Générale d'Optique) (FR) 2013-06-13 — — WO disclosed
EP-2602655-A1 Ophthalmic filter Essilor International (Compagnie Générale D'Optique) (FR) 2013-06-12 — — EP disclosed
EP-2602653-A1 Method of determining the configuration of an ophthalmic filter Essilor International (Compagnie Générale D'Optique) (FR) 2013-06-12 — — EP disclosed
EP-2602654-A1 Ophthalmic filter Essilor International (Compagnie Générale D'Optique) (FR) 2013-06-12 — — EP disclosed
EP-1704057-A1 LASER IMAGING Sherwood Technology LTD. (GB) 2006-09-27 — — EP disclosed
WO-2005068207-A1 LASER IMAGING DATALASE LTD. (GB) 2005-07-28 — — 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-11865521-B2 Bifunctional catalyst for hydrogenation of carbon dioxide, and method for preparing hydrocarbon by using same TDO2, SCO2, HAO2 TERT 58/4885TOP1 352/4885ABCG2 4720/4885

“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.

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