Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2447465

C(=CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-].[Cl-]

nearest known ligand 0.55

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 12)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 1/20 0.55
ALDH1A1 P00352 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
TSHR P16473 1/20 0.41
CYP2C19 P33261 1/20 0.41
SNCA P37840 2/20 0.38
MAOB P27338 1/20 0.36
HTR2A P28223 3/20 0.34
CHRNA7 P36544 8/20 0.34
GRIK1 P39086 1/20 0.31
GRIK2 Q13002 1/20 0.31

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 SCHEMBL14839973 1.00 HIF1A (0.55) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL8925807 0.95 HIF1A (0.55) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL11255368 0.86 HIF1A (0.46) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL2445999 0.86 HIF1A (0.46) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL2446001 0.86 HIF1A (0.46) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL16004643 0.84 HIF1A (0.44) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL2452746 0.84 HTR2A (0.50) HIF1AHTR2ACHRNA7GRIK1GRIK2
Bromide SCHEMBL11584557 0.84 HIF1A (0.44) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL2452749 0.84 HTR2A (0.50) HIF1AHTR2ACHRNA7GRIK1GRIK2
Hydrochloric Acid SCHEMBL11732846 0.83 HIF1A (0.43) HIF1AALDH1A1CYP1A2CYP2D6TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10928728-B2 Photoactivable nitrogen bases BASF SE (DE) 2021-02-23 US disclosed
US-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2021-02-04 US disclosed
US-20180217498-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2018-08-02 US disclosed
US-9921477-B2 Photoactivable nitrogen bases BASE SE (DE) 2018-03-20 US disclosed
EP-2145231-B1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2011-09-14 EP disclosed
US-20100105794-A1 PHOTOACTIVABLE NITROGEN BASES CIBA CORPORATION (US) 2010-04-29 US disclosed
EP-2145231-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2010-01-20 EP disclosed
WO-2008119688-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (CH) 2008-10-09 WO disclosed
EP-0970085-B1 PHOTOACTIVATABLE NITROGEN-CONTAINING BASES BASED ON ALPHA-AMINO ALKENES CIBA SC HOLDING AG (CH) 2002-07-24 EP disclosed
US-6087070-A AS PHOTOINITIATORS FOR BASE-CATALYZABLE REACTIONS CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-07-11 US disclosed
EP-0970085-A1 PHOTOACTIVATABLE NITROGEN-CONTAINING BASES BASED ON $g(a)-AMINO ALKENES Ciba SC Holding AG (CH) 2000-01-12 EP disclosed
WO-1998041524-A1 PHOTOACTIVATABLE NITROGEN-CONTAINING BASES BASED ON α-AMINO ALKENES CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 1998-09-24 WO disclosed
US-5097022-A Bisazo pigments for use in electrophotographic photoconductors RICOH COMPANY, LTD. (JP) 1992-03-17 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-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES CBR1, ARNT, NR0B1 HIF1A 1258/4885ALDH1A1 1659/4885CYP1A2 73/4885
US-10928728-B2 Photoactivable nitrogen bases CBR1, NR0B1, NR0B2 HIF1A 1136/4885ALDH1A1 1733/4885CYP1A2 81/4885
US-20180217498-A1 PHOTOACTIVABLE NITROGEN BASES CBR1, NR0B1, NR0B2 HIF1A 1136/4885ALDH1A1 1733/4885CYP1A2 81/4885

“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.