Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6930183

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

nearest known ligand 0.37

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
SLC6A2 known ✓ P23975 1/20 0.31
KIF11 P52732 2/20 0.37
TSHR P16473 1/20 0.36
CYP19A1 P11511 2/20 0.35
HTR1D P28221 1/20 0.33
ADRA1A P35348 1/20 0.33
NISCH Q9Y2I1 1/20 0.33
HSD11B1 P28845 1/20 0.32
FGF23 Q9GZV9 1/20 0.32
KMT2A Q03164 3/20 0.32
MEN1 O00255 1/20 0.32
RAB9A P51151 1/20 0.32
KDM4E B2RXH2 1/20 0.31
ALDH1A1 P00352 1/20 0.31
TP53 P04637 1/20 0.31
TNKS O95271 1/20 0.31
TNKS2 Q9H2K2 1/20 0.31
HDAC6 Q9UBN7 1/20 0.31
TNF P01375 1/20 0.31
NOD1 Q9Y239 1/20 0.31

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 SCHEMBL6928610 0.79 KIF11 (0.37) KIF11TSHRCYP19A1HTR1DADRA1A
Hydrochloric Acid SCHEMBL6287543 0.79 PTGS2 (0.33) NISCHRAB9AKDM4EALDH1A1
P-Xylene SCHEMBL1419675 0.69 TSHR (0.68) KIF11TSHRCYP19A1KMT2AMEN1
SCHEMBL128222 0.69 KIF11 (0.59) KIF11TSHRCYP19A1RAB9AALDH1A1
SCHEMBL3421942 0.69 KIF11 (0.59) KIF11TSHRCYP19A1RAB9AALDH1A1
Hydrochloric Acid SCHEMBL6290431 0.68 IKBKB (0.33)
SCHEMBL28383000 0.67 CFTR (0.44) TSHRKMT2AALDH1A1LMNA
Ethane SCHEMBL27903947 0.67 KIF11 (0.57) KIF11TSHRCYP19A1RAB9AALDH1A1
Hydrochloric Acid SCHEMBL6928540 0.66 RAB9A (0.36) TSHRCYP19A1KMT2AMEN1RAB9A
Hydrochloric Acid SCHEMBL7834977 0.65 CFTR (0.39) KMT2AALDH1A1

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