Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3278043

Cc1cc[n+](Cc2ccccc2)cc1.[Cl-]

nearest known ligand 0.79

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 10)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.79
KDM4E B2RXH2 2/20 0.79
RAB9A P51151 1/20 0.79
CHKA P35790 10/20 0.64
LMNA P02545 4/20 0.60
SMN1; SMN2 Q16637 4/20 0.60
HTT P42858 3/20 0.60
MEN1 O00255 1/20 0.47
MAPT P10636 1/20 0.47
KMT2A Q03164 1/20 0.47

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
SCHEMBL1824133 0.98 ALDH1A1 (0.75) ALDH1A1KDM4ERAB9ACHKALMNA
Bromide SCHEMBL1757103 0.96 ALDH1A1 (0.72) ALDH1A1KDM4ERAB9ACHKALMNA
SCHEMBL15164180 0.86 CHKA (0.83) ALDH1A1KDM4ERAB9ACHKALMNA
Hydrochloric Acid SCHEMBL5155076 0.83 ALDH1A1 (0.61) ALDH1A1KDM4ERAB9ACHKALMNA
Benzyl Viologen SCHEMBL1930045 0.82 ALDH1A1 (0.78) ALDH1A1KDM4ERAB9ACHKALMNA
Hydrochloric Acid SCHEMBL636283 0.81 LMNA (0.63) ALDH1A1KDM4ERAB9ACHKALMNA
Hydrochloric Acid SCHEMBL2460504 0.81 ALDH1A1 (0.79) ALDH1A1KDM4ERAB9ACHKALMNA
SCHEMBL13283227 0.81 CHKA (0.61) ALDH1A1KDM4ERAB9ACHKALMNA
Hydrochloric Acid SCHEMBL10935706 0.81 ALDH1A1 (0.55) ALDH1A1KDM4ERAB9ACHKALMNA
SCHEMBL367939 0.80 ALDH1A1 (0.63) ALDH1A1KDM4ERAB9ACHKALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7700780-B2 Zwitterionic chromophores and macromolecules containing such chromophores Wang, Zhi Yuan (CA) 2010-04-20 US disclosed
US-7592358-B2 Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-09-22 US disclosed
EP-1686130-B1 Pyrrolo[2,3-d]pyrimidine compounds as immunosuppressive agents PFIZER PROD INC (US) 2009-02-18 EP disclosed
US-20070161666-A1 Pyrrolo[2,3-d]pyrimidine compounds PFIZER INC 2007-07-12 US disclosed
US-7192963-B2 Pyrrolo[2,3-d]pyrimidine compounds PFIZER INC (US) 2007-03-20 US disclosed
EP-1742939-A2 NOVEL ALKYNE COMPOUNDS EXHIBITING AN MCH ANTAGONISTIC EFFECT AND DRUGS CONTAINING SAID COMPOUNDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-01-17 EP disclosed
EP-1740572-A1 NOVEL ALKYNE COMPOUNDS WITH AN MCH-ANTAGONISTIC ACTION AND MEDICAMENTS CONTAINING SAID COMPOUNDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-01-10 EP disclosed
EP-1737823-A2 NOVEL ALKYNE COMPOUNDS WITH AN MCH-ANTAGONISTIC ACTION AND MEDICAMENTS COMPRISING SAID COMPOUNDS Boehringer Ingelheim International GmbH (DE) 2007-01-03 EP disclosed
US-20060199951-A1 Zwitterionic chromophores and macromolecules containing such chromophores WANG ZHI Y 2006-09-07 US disclosed
EP-1686130-A1 Pyrrolo[2,3-d]pyrimidine compounds as immunosuppressive agents Pfizer Products Incorporated (US) 2006-08-02 EP disclosed
US-20030220353-A1 Pyrrolo[2,3-d]pyrimidine compounds PFIZER INC. 2003-11-27 US disclosed
EP-1294724-A1 PYRROLO[2,3-D]PYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE AGENTS Pfizer Products Inc. (US) 2003-03-26 EP disclosed
US-20020068746-A1 Pyrrolo[2,3-d]pyrimidine compounds PFIZER INC. 2002-06-06 US disclosed
WO-2002000661-A1 PYRROLO[2,3-d]PYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE AGENTS PFIZER PRODUCTS INC. (US) 2002-01-03 WO disclosed
US-5290789-A Antipsychotically effective compounds STERLING WINTROP INC. (US) 1994-03-01 US disclosed
US-5286733-A Treating psychoses STERLING WINTHROP INC. (US) 1994-02-15 US disclosed
US-4734460-A STORAGE STABILITY NIPPON MEKTRON LIMITED, A CORP. OF JAPAN 1988-03-29 US disclosed
US-4558133-A p-(Pyridinium-vinyl)-N,N-(disubstituted-aniline salts for dyeing paper and their preparation BAYER AKTIENGESELLSCHAFT (DE) 1985-12-10 US disclosed
EP-0023991-A1 Styryl dyestuffs, their preparation and their use in dyeing paper in particular BAYER AG (DE) 1981-02-18 EP disclosed
US-4032596-A QUATERNARY AMMONIUM SALTS, FREE RADICAL CATALYSTS AIR PRODUCTS AND CHEMICALS, INC. (US) 1977-06-28 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 (3 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-20030220353-A1 Pyrrolo[2,3-d]pyrimidine compounds JAK1, CDK2, JAK3 ALDH1A1 1719/4885KDM4E 1452/4885RAB9A 1772/4885
US-20020068746-A1 Pyrrolo[2,3-d]pyrimidine compounds JAK1, CDK2, JAK3 ALDH1A1 1719/4885KDM4E 1452/4885RAB9A 1772/4885
US-20070161666-A1 Pyrrolo[2,3-d]pyrimidine compounds CDK2, CDK3, JAK3 ALDH1A1 2505/4885KDM4E 1016/4885RAB9A 2542/4885

“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.