Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5041774

CCCC[P+](CCCC)(CCCC)Cc1ccc(C(=O)O)cc1.[Cl-]

nearest known ligand 0.71

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 11)

geneUniProtsupporting neighboursconfidence
▸ BDKRB2 known ✓ P30411 7/20 0.71
▸ RARB P10826 6/20 0.54
▸ ALDH1A1 P00352 2/20 0.52
▸ MEN1 O00255 1/20 0.51
▸ RARA P10276 1/20 0.51
▸ MAPT P10636 1/20 0.51
▸ MTOR P42345 1/20 0.51
▸ KMT2A Q03164 1/20 0.51
▸ FOLH1 Q04609 1/20 0.45
▸ TP53 P04637 1/20 0.45
▸ TSHR P16473 1/20 0.45

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
SCHEMBL11204396 0.80 RARB (0.54) BDKRB2RARBALDH1A1MEN1RARA
Bromide SCHEMBL30466581 0.80 BDKRB2 (0.64) BDKRB2ALDH1A1MAPT
SCHEMBL9700188 0.79 RARB (0.53) BDKRB2RARBALDH1A1MEN1RARA
Bromide SCHEMBL11601966 0.78 FOLH1 (0.50) BDKRB2FOLH1TP53
Hydrochloric Acid SCHEMBL465040 0.78 BDKRB2 (0.71) BDKRB2MEN1KMT2ATP53
Terephthalic Acid SCHEMBL28198649 0.77 RARB (0.53) RARBALDH1A1MEN1RARAMAPT
Hydrochloric Acid SCHEMBL10577821 0.77 BDKRB2 (0.75) BDKRB2
Terephthalic Acid SCHEMBL29199831 0.77 RARB (0.53) RARBALDH1A1MEN1RARAMAPT
Acetic Acid SCHEMBL16209117 0.77 BDKRB2 (0.54) BDKRB2
SCHEMBL8841547 0.76 RARB (0.62) BDKRB2RARBALDH1A1MEN1RARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1799846-A4 METHODS FOR ISOLATING NUCLEIC ACIDS FROM BIOLOGICAL AND CELLULAR MATERIALS NEXGEN DIAGNOSTICS LLC (US) 2008-01-16 — — EP disclosed
CN-101076603-A Simplified methods for isolating nucleic acids from cellular materials LUMIGEN INC (US) 2007-11-21 — — CN disclosed
EP-1799846-A2 METHODS FOR ISOLATING NUCLEIC ACIDS FROM BIOLOGICAL AND CELLULAR MATERIALS LUMIGEN, INC. (US) 2007-06-27 — — EP disclosed
WO-2006036243-A2 METHODS FOR ISOLATING NUCLEIC ACIDS FROM BIOLOGICAL AND CELLULAR MATERIALS LUMIGEN, INC. (US) 2006-04-06 — — WO disclosed
US-20050136477-A1 Methods for isolating nucleic acids from biological and cellular materials NEXGEN DIAGNOSTICS LLC 2005-06-23 — — 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-20050136477-A1 Methods for isolating nucleic acids from biological and cellular materials NSUN2, DNA2, POLB BDKRB2 4440/4885RARB 1743/4885ALDH1A1 4724/4885

“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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