Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7238971

COc1ccc(O)c(-c2ccc(-c3ccc(-c4ccc(C)cc4O)cn3)nc2)c1.[Cl-].[Cl-].[Cl-].[Mn+3]

nearest known ligand 0.50

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
KMT2A Q03164 7/20 0.50
MEN1 O00255 6/20 0.50
RAB9A P51151 5/20 0.50
MAPT P10636 3/20 0.50
LMNA P02545 3/20 0.50
CASP3 P42574 3/20 0.50
SENP7 Q9BQF6 3/20 0.50
SENP8 Q96LD8 2/20 0.50
SENP6 Q9GZR1 2/20 0.50
JAK2 O60674 1/20 0.50
NFKB1 P19838 1/20 0.50
NFKB2 Q00653 1/20 0.50
RELA Q04206 1/20 0.50
NPC1 O15118 5/20 0.47
GAA P10253 3/20 0.47
ALOX15 P16050 3/20 0.47
HPGD P15428 2/20 0.47
KDM4E B2RXH2 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
NPSR1 Q6W5P4 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
Hydrochloric Acid SCHEMBL7238375 0.95 KMT2A (0.55) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7234590 0.92 KMT2A (0.54) KMT2AMEN1RAB9AMAPTLMNA
Acetic Acid SCHEMBL7235306 0.92 KMT2A (0.46) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7232788 0.88 NPC1 (0.49) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7242130 0.87 IDO1 (0.47) KMT2AMEN1RAB9AMAPTLMNA
Acetic Acid SCHEMBL7235881 0.86 KMT2A (0.50) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7235242 0.85 NPC1 (0.56) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7235427 0.85 GAA (0.44) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7232404 0.84 NPC1 (0.51) KMT2AMEN1RAB9AMAPTLMNA
Hydrochloric Acid SCHEMBL7234791 0.84 MEN1 (0.46) KMT2AMEN1RAB9AMAPTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6541490-B1 Treating ischemia or reoxygenation injury; preparation from a bipyridine, a benzeneboronic acid and a manganese salt EUKARION, INC. 2003-04-01 US disclosed
EP-1119573-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2001-08-01 EP disclosed
US-6177419-B1 ANTIOXIDANT CHELATE COMPOUNDS FOR PREVENTING OXYGEN FREE RADICAL-ASSOCIATED DISEASES IN MAMMALS; NEUROPROTECTANTS, SUPEROXIDE DISMUTASE (SOD), CATALASE (CAT) AND/OR PEROXIDASE (POD) MIMETICS EUKARION, INC. 2001-01-23 US disclosed
WO-2000009512-A2 BIPYRIDINE MANGANESE COMPLEXES EUKARION, INC. (US) 2000-02-24 WO disclosed