Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8672876

CC(=O)S[C@H](O)C[N+](C)(C)C.[Cl-]

nearest known ligand 0.45

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
CHRM1 known ✓ P11229 3/20 0.39
CHRM2 known ✓ P08172 2/20 0.39
CHRM3 known ✓ P20309 2/20 0.33
MAPT P10636 3/20 0.45
BLM P54132 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
GALR3 O60755 1/20 0.42
POLB P06746 1/20 0.40
ATM Q13315 1/20 0.40
SLC22A16 Q86VW1 1/20 0.40
TSHR P16473 2/20 0.39
CHRM4 P08173 2/20 0.39
TBXA2R P21731 1/20 0.39
LMNA P02545 4/20 0.37
CYP2C19 P33261 1/20 0.37
CHRM5 P08912 2/20 0.33
CPT2 P23786 1/20 0.33
CPT1A P50416 1/20 0.33
MEN1 O00255 1/20 0.33
CYP1A2 P05177 1/20 0.33

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 SCHEMBL1276371 1.00 MAPT (0.45) MAPTBLMSMN1; SMN2GALR3POLB
SCHEMBL6153646 0.98 MAPT (0.41) MAPTBLMSMN1; SMN2GALR3POLB
SCHEMBL77665 0.98 MAPT (0.41) MAPTBLMSMN1; SMN2GALR3POLB
Water SCHEMBL16322375 0.95 MAPT (0.40) MAPTBLMSMN1; SMN2GALR3POLB
Bromide SCHEMBL7172545 0.95 MAPT (0.40) MAPTBLMSMN1; SMN2GALR3POLB
Bromide SCHEMBL9233901 0.95 MAPT (0.40) MAPTBLMSMN1; SMN2GALR3POLB
SCHEMBL4318608 0.95 MAPT (0.40) MAPTBLMSMN1; SMN2GALR3POLB
Iodide SCHEMBL400576 0.95 MAPT (0.40) MAPTBLMSMN1; SMN2GALR3POLB
Perchlorate SCHEMBL9097182 0.90 SLC22A16 (0.41) MAPTBLMSMN1; SMN2GALR3POLB
SCHEMBL8055941 0.76 MAPT (0.39) MAPTBLMSMN1; SMN2GALR3SLC22A16

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5726323-A COMPOUNDS USEFUL FOR ALLEVIATING MEMORY DYSFUNCTIONS HOECHST MARION ROUSSEL, INC. 1998-03-10 US disclosed
US-5663190-A INHIBITORS OF ACETYLCHOLINESTERASE, TREATMENT OF ALZHEIMER*S DISEASE HOECHST MARION ROUSSEL, INC. (US) 1997-09-02 US disclosed
EP-0420140-B1 N-Aminocarbamates related to physostigmine, a process for their preparation and their use as medicaments HOECHST MARION ROUSSEL INC (US) 1997-08-13 EP disclosed
US-5639892-A ANTIDEPRESSANTS, ALZHEIMER'S DISEASE HOECHST-MARION-ROUSSEL, INC. (US) 1997-06-17 US disclosed
US-5621114-A REACTING A THIO OR PHENOL COMPOUND WITH 1,1-CARBONYLIMIDAZOLE OR 1,1-THIOCARBONYLDIIMIDAZOLE, REACTING THE INTERMEDIATE WITH SECONDARY AMINE COMPOUND; USEFUL AS ANALGESIC AND MEMORY ENHANCING AGENT HOECHST MARION ROUSSEL, INC. (US) 1997-04-15 US disclosed
US-5591864-A CHEMICAL INTERMEDIATES FOR COMPOUNDS WHICH ALLEVIATE MEMORY DYSFUNCITONS HOECHST MARION ROUSSEL, INC. (US) 1997-01-07 US disclosed
EP-0430201-B1 Aminocarbonylcarbamates related to physostigmine, a process for their preparation and their use as medicaments HOECHST ROUSSEL PHARMA (US) 1996-09-18 EP disclosed
US-5550254-A REACTING CARBOXYLIC ACID WITH CARBONYLDIIMIDAZOLE OR THIOCARBONYLDIIMIDAZOLE, ADDING PHENOL OR THIOPHENOL COMPOUND HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) 1996-08-27 US disclosed
US-5550253-A REACTING PHENOL OR THIOPHENOL DERIVATIVE WITH LOWER ALKYL P-TOLUENESULFONATE, OPTIONALLY REDUCING NITRO GROUPS TO AMINO GROUPS AND ACYLATING OR ALKYLATING THEM HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) 1996-08-27 US disclosed
US-5547977-A Memory enhancing and analgesic 1,2,3,3A,8,8A-hexahydro-3A,8(and 1,3A,8)-di (and Tri) methylpyrrolo (2,3-B) indoles HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) 1996-08-20 US disclosed
US-5077289-A Cholinergic function enhancers HOECHST ROUSSEL PHARMACEUTICALS INC. (US) 1991-12-31 US disclosed
EP-0440145-A1 Hexahydropyrrolo[2,3-b]indole carbamates,-ureas,-amides and related compounds, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-08-07 EP disclosed
EP-0430201-A2 Aminocarbonylcarbamates related to physostigmine, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-06-05 EP disclosed
US-5010083-A Cognition activator; Alzheimer*s disease HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) 1991-04-23 US disclosed
EP-0420140-A2 N-Aminocarbamates related to physostigmine, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-04-03 EP disclosed
US-4983616-A Analgesics, cognition activators HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1991-01-08 US disclosed
US-4937341-A Process for preparing N-aminocarbarbamates related to physostigmine HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1990-06-26 US disclosed
US-4914102-A ALLEVIATING MEMORY DYSFUNCTIONS CHARACTERIZED BY CHOLINERGIC DEFICIT HOECHST ROUSSEL PHARMACEUTICALS, INC. (US) 1990-04-03 US disclosed
US-4791107-A Memory enhancing and analgesic 1,2,3,3A,8,8A-hexahydro-3A,8 (and) 1,3A,8)-di(and tri)methylpyrrolo(2,3-B)indoles, compositions and use HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) 1988-12-13 US disclosed
EP-0253372-A2 1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indoles, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1988-01-20 EP disclosed