Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6928540

CC1=C(C)C([Hf+2]C2=C(c3ccc(C)cc3)CC(C)=C2C)=C(c2ccccc2)C1.[Cl-].[Cl-]

nearest known ligand 0.36

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
ACHE known ✓ P22303 1/20 0.32
RAB9A P51151 5/20 0.36
NPC1 O15118 4/20 0.36
TDP1 Q9NUW8 2/20 0.36
HPGD P15428 2/20 0.36
NFKB1 P19838 2/20 0.36
NFKB2 Q00653 2/20 0.36
RELA Q04206 2/20 0.36
POLB P06746 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
ALDH1A1 P00352 3/20 0.36
KDM4E B2RXH2 2/20 0.36
MEN1 O00255 3/20 0.33
KMT2A Q03164 3/20 0.33
CFTR P13569 1/20 0.33
GOPC Q9HD26 1/20 0.33
MAPT P10636 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
CYP19A1 P11511 1/20 0.33
NTSR1 P30989 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 SCHEMBL6286838 0.93 PTGS2 (0.33) TDP1ACHEPTGS1PTGS2
Hydrochloric Acid SCHEMBL6928610 0.84 KIF11 (0.37) RAB9AALDH1A1KDM4EMEN1KMT2A
Hydrochloric Acid SCHEMBL6286926 0.72 CFTR (0.38) TDP1HPGDALDH1A1KDM4EMEN1
Hydrochloric Acid SCHEMBL7834977 0.69 CFTR (0.39) ALDH1A1KMT2ACFTRGOPCACHE
Hydrochloric Acid SCHEMBL6287543 0.69 PTGS2 (0.33) RAB9ATDP1ALDH1A1KDM4EACHE
SCHEMBL27949026 0.69 PTGS2 (0.42) ALDH1A1KMT2ACFTRGOPCPTGS1
Hydrochloric Acid SCHEMBL27790671 0.66 ACHE (0.56) RAB9ANPC1TDP1HPGDNFKB1
SCHEMBL5606620 0.66 PTGS2 (0.53) RAB9ANPC1TDP1HPGDNFKB1
SCHEMBL587 0.66 ACHE (0.62) RAB9ANPC1TDP1HPGDNFKB1
SCHEMBL22079642 0.66 ACHE (0.62) RAB9ANPC1TDP1HPGDNFKB1

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
US-6518378-B2 Using an unbridged cyclopentadienyl metallocene catalyst capable of interconverting between states with different copolymerization characteristics THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2003-02-11 US disclosed
US-6479685-B2 POLYMERIZING ETHYLENE AND ANOTHER ALPHA-OLEFIN IN THE PRESENCE OF AN UNBRIDGED, ROTATING, NON-RIGID FLUXIONAL METALLOCENE CATALYST COMPONENT AND A CO-CATALYST THE BOARD OF TRUSTEES OF THE LELAND STANDARD JUNIOR UNIVERSITY 2002-11-12 US disclosed
US-20010049425-A1 High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis BP CORPORATION NORTH AMERICA INC. 2001-12-06 US disclosed
US-20010034426-A1 High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis BP CORPORATION NORTH AMERICA INC. 2001-10-25 US disclosed
US-6169151-B1 MADE BY POLYMERIZING ETHYLENE AND ALPHA-OLEFIN(S) USING AN UNBRIDGED, ROTATING, NON-RIGID FLUXIONAL METALLOCENE CATALYST AND COCATALYST; CRYSTALLIZABLE ELASTOMERIC COPOLYMER PRODUCT HAS HIGHER MELTING POINT, NARROW COMPOSITION DISTRIBUTION THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2001-01-02 US disclosed