Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1465445

C1=Cc2nc1c(-c1ccccc1)c1ccc([nH]1)c(-c1ccccc1)c1nc(c(-c3ccccc3)c3ccc([nH]3)c2-c2ccccc2)C=C1.[Cl-].[Cl-].[Cl-].[Fe+3]

nearest known ligand 0.60

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
▸ TOP1 P11387 4/20 0.60
▸ STAT3 P40763 1/20 0.59
▸ STAT1 P42224 1/20 0.59
▸ CYCS P99999 3/20 0.58
▸ TERT O14746 4/20 0.58
▸ ENPP2 Q13822 1/20 0.53

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
Tetraphenylporphyrin SCHEMBL30148173 0.98 CYCS (0.61) TOP1STAT3STAT1CYCSTERT
Tetraphenylporphyrin SCHEMBL30148172 0.98 CYCS (0.61) TOP1STAT3STAT1CYCSTERT
SCHEMBL29405816 0.98 TOP1 (0.62) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL30306704 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL29440936 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL29872728 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL483551 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL483749 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL30909509 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT
Hydrochloric Acid SCHEMBL483505 0.96 TOP1 (0.60) TOP1STAT3STAT1CYCSTERT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109755504-A Application containing ferriporphyrin/carbon/carbon nano tube compound anode material preparation method and its in lithium-sulphur cell positive electrode 温州大学 2019-05-14 — — CN claimed
CN-107417535-B A kind of one-pot synthesis method of highly selective (E)-beta-nitrostyrene derivative 沅江华龙催化科技有限公司 2019-04-09 — — CN claimed
CN-107098811-B (E)-beta-nitrostyrene synthetic method 沅江华龙催化科技有限公司 2019-03-26 — — CN claimed
CN-106995373-B Using ammonium iodide as nitro source one-pot synthesis α, β-unsaturation nitroolefin derivative method 沅江华龙催化科技有限公司 2019-01-11 — — CN claimed
CN-106995372-B A method of (E)-beta-nitrostyrene derivative is catalyzed and synthesized based on tetaraary porphyrin iron 沅江华龙催化科技有限公司 2018-12-18 — — CN 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-107417535-A A kind of One-step Synthesis method of high selectivity (E) β nitrostyrene derivatives 沅江华龙催化科技有限公司 2017-12-01 — — CN claimed
CN-107098811-A (E) synthetic method of β nitrostyrolenes 沅江华龙催化科技有限公司 2017-08-29 — — CN claimed
CN-107032939-A The synthetic method of α, β unsaturation nitroolefin derivative 沅江华龙催化科技有限公司 2017-08-11 — — CN claimed
CN-106995372-A One kind is catalyzed and synthesized based on tetaraary porphyrin iron(E)The method of β nitrostyrene derivatives 沅江华龙催化科技有限公司 2017-08-01 — — CN claimed
US-20040041082-A1 Molecular sensing array BANK OF THE WEST 2004-03-04 — — US claimed
JP-2002510305-A — — 2002-04-02 — — JP claimed
EP-1062221-A4 PROCESS FOR MAKING GLYPHOSATE BY OXIDIZING N-SUBSTITUTED GLYPHOSATES MONSANTO TECHNOLOGY LLC (US) 2001-10-17 — — EP claimed
US-20010018536-A1 Process for the preparation of n- (phosphonomethyl) glycine by oxidizing n-substituted n-(phosphonomethyl) glycine MONSANTO TECHNOLOGY LLC 2001-08-30 — — US claimed
US-6245707-B1 HEAT TREATED ELECTROCATALYST MIXTURE OF TWO DIFFERENT CHELATE COMPOUNDS COMPRISING NITROGENOUS LIGAND-CHELATED TRANSITION METALS OTHER THAN PLATINUM OR PALLADIUM; IMPROVED OXYGEN REDUCTION AT A FUEL CELL CATHODE AFTER METHANOL CROSSOVER THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY 2001-06-12 — — US claimed
US-6232494-B1 CATALYTIC OXIDATION MONSANTO COMPANY 2001-05-15 — — US claimed
EP-1062221-A1 PROCESS FOR MAKING GLYPHOSATE BY OXIDIZING N-SUBSTITUTED GLYPHOSATES MONSANTO COMPANY (US) 2000-12-27 — — EP claimed
US-6005140-A USING A NOBLE METAL OXIDATION CATALYST MONSANTO COMPANY (US) 1999-12-21 — — US claimed
WO-1999041260-A1 PROCESS FOR MAKING GLYPHOSATE BY OXIDIZING N-SUBSTITUTED GLYPHOSATES MONSANTO COMPANY (US) 1999-08-19 — — WO claimed
US-5444134-A Using a coordination catalyst IDEMITSU KOSAN CO., LTD. (JP) 1995-08-22 — — US claimed

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-20010018536-A1 Process for the preparation of n- (phosphonomethyl) glycine by oxidizing n-substituted n-(phosphonomethyl) glycine GNMT, GRHPR, GLRA3 TOP1 3870/4885STAT3 2155/4885STAT1 1351/4885

“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.

Send feedback