Hydrochloric Acid

Hydrochloric Acid

SCHEMBL10698899

[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Sn].[Sn].[Sn].[Sn].[Sn].[V+5].[V+5].c1ccc([Al-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.c1ccc([Al-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.c1ccc([Al-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.c1ccc([Al-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.c1ccc([Al-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.33

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 16)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.30
ALDH1A1 P00352 2/20 0.33
NOTUM Q6P988 1/20 0.30
TSHR P16473 3/20 0.30
CA1 P00915 2/20 0.30
CA2 P00918 2/20 0.30
CA9 Q16790 2/20 0.30
TDP1 Q9NUW8 2/20 0.30
CA12 O43570 1/20 0.30
GLA P06280 1/20 0.30
CA3 P07451 1/20 0.30
CA4 P22748 1/20 0.30
CA14 Q9ULX7 1/20 0.30
LMNA P02545 1/20 0.30
ALOX12 P18054 1/20 0.30
CA7 P43166 1/20 0.30

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
SCHEMBL689950 0.89 ALDH1A1 (0.40) ALDH1A1TSHRCA1CA2CA9
Potassium Ion SCHEMBL135041 0.89 ALDH1A1 (0.40) ALDH1A1TSHRCA1CA2CA9
Lithium Ion SCHEMBL132837 0.86 ALDH1A1 (0.38) ALDH1A1TSHRCA1CA2CA9
SCHEMBL137469 0.86 ALDH1A1 (0.38) ALDH1A1TSHRCA1CA2CA9
Methoxymethane SCHEMBL7621929 0.78 TSHR (0.35) ALDH1A1TSHRCA4LMNAALOX12
SCHEMBL297115 0.78 TSHR (0.35) ALDH1A1TSHRCA4LMNAALOX12
Trimethylammonium SCHEMBL297595 0.78 TSHR (0.35) ALDH1A1TSHRCA4LMNAALOX12
Tetraphenylphosphonium SCHEMBL10884651 0.73 HIF1A (0.38)
SCHEMBL298043 0.73
SCHEMBL10882084 0.73

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0257765-A1 Cold flow improver and method of use thereof PETROLITE CORPORATION (US) 1988-03-02 EP disclosed
US-4708993-A OLIGOMERS OF ESTER-CONTAINING HALOPOLYALKYENES AS OIL OR FUEL ADDITIVES PETROLITE CORPORATION (US) 1987-11-24 US disclosed
US-4617025-A POUR POINT DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1986-10-14 US disclosed
US-4568359-A FUEL OIL POUR DEPRESSANTS PETROLITE CORPORATION (US) 1986-02-04 US disclosed
US-4568726-A REACTING HALOGENATED POLYALKENE WITH CARBOXYLIC ACID OR SALT; POUR DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1986-02-04 US disclosed
US-4553980-A POUR DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1985-11-19 US disclosed
US-4554327-A ESTERIFIED HALOGENATED POLYOLEFIN PETROLITE CORPORATION (US) 1985-11-19 US disclosed
US-4544712-A POUR DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1985-10-01 US disclosed
US-4541839-A POUR POINT DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1985-09-17 US disclosed
US-4536551-A FREE OF CROSSLINKING; POUR DEPRESSSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1985-08-20 US disclosed
US-4536191-A FOUR POINT DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1985-08-20 US disclosed
US-4471098-A REACTION OF HALOGENATED POLYALKENE WITH CARBOXY ACID SALT, REPLACES HALO GROUPS WITH ESTER GROUPS, POUR DEPRESSANTS FOR FUEL OILS PETROLITE CORPORATION (US) 1984-09-11 US disclosed