Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2229624

COC(=O)c1ccc(OC)c(NC(=N)N)c1.[Cl-].[H+]

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 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.55
KMT2A Q03164 6/20 0.50
MEN1 O00255 3/20 0.50
CYP2C9 P11712 2/20 0.50
ALDH1A1 P00352 3/20 0.48
CYP1A2 P05177 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
POLB P06746 1/20 0.48
KDM4E B2RXH2 2/20 0.48
TP53 P04637 1/20 0.48
GAA P10253 1/20 0.48
TSHR P16473 1/20 0.47
HSD17B10 Q99714 1/20 0.47
HDAC1 Q13547 2/20 0.47
HDAC8 Q9BY41 2/20 0.47
HDAC6 Q9UBN7 2/20 0.47
MDH1 P40925 1/20 0.46
MDH2 P40926 1/20 0.46
CREBBP Q92793 1/20 0.46

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
SCHEMBL13425100 0.97 MAPT (0.58) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL10748020 0.86 MAPT (0.59) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL1554272 0.85 MAPT (0.54) MAPTKMT2AMEN1CYP2C9ALDH1A1
Hydrochloric Acid SCHEMBL8887973 0.84 CA12 (0.60) KMT2AMEN1CYP1A2L3MBTL1POLB
SCHEMBL3044520 0.84 MAPT (0.56) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL12444992 0.84 MAPT (0.56) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL13425267 0.83 MAPT (0.52) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL28649485 0.81 MAPT (0.57) MAPTKMT2AMEN1CYP2C9ALDH1A1
SCHEMBL6266977 0.81 TP53 (0.69) MAPTKMT2AALDH1A1POLBKDM4E
SCHEMBL1553365 0.81 ALDH1A1 (0.52) MAPTKMT2AMEN1CYP2C9ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110183975-A1 NOVEL 6-AZAINDOLE AMINOPYRIMIDINE DERIVATIVES HAVING NIK INHIBITORY ACTIVITY GOTO YASUHIRO 2011-07-28 US disclosed
WO-2010042337-A1 NOVEL 6-AZAINDOLE AMINOPYRIMIDINE DERIVATIVES HAVING NIK INHIBITORY ACTIVITY MERCK SHARP & DOHME CORP. (US) 2010-04-15 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-20110183975-A1 NOVEL 6-AZAINDOLE AMINOPYRIMIDINE DERIVATIVES HAVING NIK INHIBITORY ACTIVITY BRIX1, REL, CNKSR1 MAPT 4634/4885KMT2A 2505/4885MEN1 2984/4885

“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.