Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2651099

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

nearest known ligand 0.86

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
ACHE known ✓ P22303 1/20 0.32
TDP1 Q9NUW8 3/20 0.86
CYP3A4 P08684 1/20 0.86
ESR1 P03372 4/20 0.60
ESR2 Q92731 4/20 0.60
KDM4E B2RXH2 1/20 0.52
GAA P10253 1/20 0.52
NPSR1 Q6W5P4 1/20 0.35
ALDH1A1 P00352 3/20 0.35
DRD1 P21728 2/20 0.34
NOTUM Q6P988 1/20 0.32
TSHR P16473 3/20 0.32
CA1 P00915 2/20 0.32
CA2 P00918 2/20 0.32
CA9 Q16790 2/20 0.32
LMNA P02545 2/20 0.32
CA12 O43570 1/20 0.32
GLA P06280 1/20 0.32
CA3 P07451 1/20 0.32
CA4 P22748 1/20 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 SCHEMBL10878421 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL201810 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL3932 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL7591449 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL7006332 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL31438532 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL8875 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL6232190 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL14714623 1.00 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL1525005 0.97 TDP1 (0.80) TDP1CYP3A4ESR1ESR2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3937857-A THERMAL DECOMPOSITION, NONCONDUCTIVE SUBSTRATE AMP INCORPORATED (US) 1976-02-10 US claimed
US-8242307-B1 Site-specific cleavage of nucleic acids by photoreactive conjugates FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 2012-08-14 US disclosed
US-20100256390-A1 PROCESSES FOR THE PREPARATION OF PYRAZOLES SYNGENTA CROP PROTECTION, INC. (US) 2010-10-07 US disclosed
US-7695912-B1 Site-specific cleavage of nucleic acids by photoreactive conjugates FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 2010-04-13 US disclosed
EP-2170832-A2 PROCESSES FOR THE PREPARATION OF PYRAZOLES Syngeta Participations AG (CH) 2010-04-07 EP disclosed
EP-2008996-A1 Process for the production of pyrazoles Syngeta Participations AG (CH) 2008-12-31 EP disclosed
WO-2009000442-A2 PROCESSES FOR THE PREPARATION OF PYRAZOLES SYNGENTA PARTICIPATIONS AG (CH) 2008-12-31 WO disclosed
EP-1999127-A1 PHTHALAZINONE PYRAZOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS F.HOFFMANN-LA ROCHE AG (CH) 2008-12-10 EP disclosed
WO-2007107298-A1 PHTHALAZINONE PYRAZOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS F. HOFFMANN-LA ROCHE AG (CH) 2007-09-27 WO disclosed
EP-1794148-A1 NOVEL PHTHALAZINONE DERIVATIVES, AS AURORA-A KINASE INHIBITORS F.HOFFMANN-LA ROCHE AG (CH) 2007-06-13 EP disclosed
EP-0364797-B1 N-aryl-nitrogenated heterocycles, process for their preparation and their use as herbicides BAYER AG (DE) 1994-02-16 EP disclosed
US-5221318-A Crop plant selectivity BAYER AKTIENGESELLSCHAFT (DE) 1993-06-22 US disclosed
US-5149834-A Anticholesterol agent and enzyme inhibitors, for curing arteriosclerosis FUJIREBIO INC. (JP) 1992-09-22 US disclosed
EP-0445827-A2 4-Hydroxytetrahydropyran-2-one derivatives useful as cholesterol and lipid reducing agents FUJIREBIO INC. (JP) 1991-09-11 EP disclosed
US-5008267-A Pyrimidinedione compounds, method of producing the same and antiarrythmic agents containing the same MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1991-04-16 US disclosed
EP-0382034-A1 N-aryl-nitrogenated heterocycles BAYER AG (DE) 1990-08-16 EP disclosed
EP-0369627-A2 Pyrimidinedione derivative compounds, method of producing the same and antiarrythmic agents containing the same MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-05-23 EP disclosed
EP-0272420-A2 Photopatterned aromatic polymeric substrates, method for making same and use GENERAL ELECTRIC COMPANY (US) 1988-06-29 EP disclosed
US-4006047-A Catalysts for electroless deposition of metals on comparatively low-temperature polyolefin and polyester substrates AMP INCORPORATED (US) 1977-02-01 US disclosed
US-3937857-A THERMAL DECOMPOSITION, NONCONDUCTIVE SUBSTRATE AMP INCORPORATED (US) 1976-02-10 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 (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-20100256390-A1 PROCESSES FOR THE PREPARATION OF PYRAZOLES CYP2F1, CYP4F3, CYP4F11 ACHE 2100/4885TDP1 2622/4885CYP3A4 7/4885

“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.