Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3937684

CC[n+]1csc2ccccc21.[Cl-]

nearest known ligand 0.58

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
MAPT P10636 10/20 0.58
ALDH1A1 P00352 7/20 0.58
KDM4E B2RXH2 7/20 0.58
HPGD P15428 5/20 0.58
MEN1 O00255 5/20 0.58
KMT2A Q03164 5/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
ALOX12 P18054 1/20 0.51
LMNA P02545 2/20 0.47
HTT P42858 2/20 0.34
RAB9A P51151 2/20 0.34
NPC1 O15118 1/20 0.34
POLB P06746 1/20 0.34
GAA P10253 1/20 0.34
NR2F2 P24468 1/20 0.34
RAD52 P43351 1/20 0.34
THRB P10828 1/20 0.32
MMP14 P50281 1/20 0.32
INSR P06213 1/20 0.31
CYP2A6 P11509 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
SCHEMBL7251667 0.98 MAPT (0.59) MAPTALDH1A1KDM4EHPGDMEN1
Bromide SCHEMBL1797564 0.96 MAPT (0.62) MAPTALDH1A1KDM4EHPGDMEN1
Iodide SCHEMBL3292667 0.96 KDM4E (0.58) MAPTALDH1A1KDM4EHPGDMEN1
Perchlorate SCHEMBL29645224 0.91 MAPT (0.53) MAPTALDH1A1KDM4EHPGDMEN1
SCHEMBL22320978 0.91 KDM4E (0.53) MAPTALDH1A1KDM4EHPGDMEN1
SCHEMBL22320973 0.91 MAPT (0.53) MAPTALDH1A1KDM4EHPGDMEN1
Perchlorate SCHEMBL5072708 0.91 MAPT (0.53) MAPTALDH1A1KDM4EHPGDMEN1
SCHEMBL5678577 0.82 KDM4E (0.56) MAPTALDH1A1KDM4EHPGDMEN1
Hydrochloric Acid SCHEMBL14333471 0.82 KDM4E (0.51) MAPTALDH1A1KDM4EHPGDMEN1
Trifluoromethanesulfonic Acid SCHEMBL22320986 0.81 KDM4E (0.44) MAPTALDH1A1KDM4EHPGDMEN1

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-2044013-B1 PROCESS FOR PRODUCING 2-HYDROXY-4-(METHYLTHIO)BUTYRATE COMPOUNDS AND INTERMEDIATES THEREOF SUMITOMO CHEMICAL CO (JP) 2013-05-29 EP disclosed
CN-102702046-A Process for producing 2-hydroxy-4-(methylthio) butyrate compounds and intermediates thereof SUMITOMO CHEMICAL CO 2012-10-03 CN disclosed
US-20090192328-A1 PROCESS FOR PRODUCING 2-HYDROXY-4-(METHLTHIO)BUTYRATE COMPOUNDS AND INTERMEDIATES THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-07-30 US disclosed
EP-2044013-A1 PROCESS FOR PRODUCING 2-HYDROXY-4-(METHYLTHIO)BUTYRATE COMPOUNDS AND INTERMEDIATES THEREOF Sumitomo Chemical Company, Limited (JP) 2009-04-08 EP disclosed
WO-2008010609-A1 PROCESS FOR PRODUCING 2-HYDROXY-4-(METHYLTHIO)BUTYRATE COMPOUNDS AND INTERMEDIATES THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2008-01-24 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-20090192328-A1 PROCESS FOR PRODUCING 2-HYDROXY-4-(METHLTHIO)BUTYRATE COMPOUNDS AND INTERMEDIATES THEREOF HAO2, BBOX1, HAO1 MAPT 2728/4885ALDH1A1 35/4885KDM4E 1863/4885

“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.