Hydrochloric Acid

Hydrochloric Acid

SCHEMBL22345579

C[n+]1cc(CCC(=O)O)c2ccccc2n1.[Cl-]

nearest known ligand 0.45

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
▸ CHRM1 known ✓ P11229 1/20 0.39
▸ HDAC6 Q9UBN7 8/20 0.45
▸ PARP1 P09874 2/20 0.43
▸ PARP2 Q9UGN5 1/20 0.43
▸ L3MBTL1 Q9Y468 1/20 0.40
▸ KEAP1 Q14145 2/20 0.40
▸ PTGER1 P34995 1/20 0.39
▸ PTGER4 P35408 1/20 0.39
▸ PTGER3 P43115 1/20 0.39
▸ PTGER2 P43116 1/20 0.39
▸ NPSR1 Q6W5P4 2/20 0.39
▸ RXFP1 Q9HBX9 2/20 0.39
▸ PRNP P04156 1/20 0.39
▸ TSHR P16473 1/20 0.39
▸ MAPK10 P53779 1/20 0.39
▸ FFAR1 O14842 1/20 0.38
▸ NFE2L2 Q16236 1/20 0.37
▸ POLB P06746 1/20 0.36
▸ HTT P42858 1/20 0.36

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
SCHEMBL28634474 0.98 HDAC6 (0.46) HDAC6PARP1PARP2L3MBTL1KEAP1
Trifluoroacetic Acid SCHEMBL22345557 0.88 HDAC6 (0.39) HDAC6PARP1PARP2L3MBTL1KEAP1
SCHEMBL22345577 0.85 HDAC6 (0.33) HDAC6PARP1PARP2NPSR1RXFP1
Iodide SCHEMBL22345444 0.82 KDM4E (0.46) RXFP1TSHRPOLB
SCHEMBL22345559 0.77 CYP4F2 (0.34) L3MBTL1RXFP1
Hydrochloric Acid SCHEMBL22345544 0.74 CYP2C9 (0.52) L3MBTL1RXFP1PRNPFFAR1POLB
SCHEMBL22345375 0.74 ACP3 (0.47) —
SCHEMBL1650885 0.73 CYP1A2 (0.55) HDAC6PARP1PARP2KEAP1CHRM1
SCHEMBL22345481 0.70 TBXAS1 (0.37) NPSR1POLB
Hydrochloric Acid SCHEMBL28623589 0.70 USP5 (0.33) RXFP1PRNPTSHRHTT

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220132847-A1 CINNOLINIUM COMPOUNDS FOR USE IN A METHOD OF CONTROLLING UNWANTED PLANT GROWTH SYNGENTA CROP PROTECTION AG (CH) 2022-05-05 — — US disclosed
EP-3924344-A1 CINNOLINIUM COMPOUNDS FOR USE IN A METHOD OF CONTROLLING UNWANTED PLANT GROWTH Syngenta Crop Protection AG (CH) 2021-12-22 — — EP disclosed
CN-113423694-A Cinnolinium compounds for use in a method for controlling unwanted plant growth 先正达农作物保护股份公司 2021-09-21 — — CN disclosed
WO-2020164970-A1 CINNOLINIUM COMPOUNDS FOR USE IN A METHOD OF CONTROLLING UNWANTED PLANT GROWTH SYNGENTA CROP PROTECTION AG (CH) 2020-08-20 — — 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-20220132847-A1 CINNOLINIUM COMPOUNDS FOR USE IN A METHOD OF CONTROLLING UNWANTED PLANT GROWTH NOTUM, DDT, CYP51A1 CHRM1 2465/4885HDAC6 2293/4885PARP1 3070/4885

“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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