Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3689983

CCCCCCC1=C2c3c(-c4ccc(CCCCCC)cc4)cccc3C1[Zr+2]C1C(CCCCCC)=C(c3c(-c4ccc(CCCCCC)cc4)cccc31)[Si]2(C)C.[Cl-].[Cl-]

nearest known ligand 0.34

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 3/20 0.33
SLC6A3 known ✓ Q01959 2/20 0.33
CHRM2 known ✓ P08172 1/20 0.33
CHRM1 known ✓ P11229 1/20 0.33
CHRM3 known ✓ P20309 1/20 0.33
ACHE known ✓ P22303 1/20 0.33
HSD17B10 Q99714 3/20 0.34
TSHR P16473 1/20 0.34
RARB P10826 7/20 0.34
ALDH1A1 P00352 3/20 0.34
MEN1 O00255 2/20 0.34
MAPT P10636 2/20 0.34
KMT2A Q03164 2/20 0.34
RARA P10276 1/20 0.34
MTOR P42345 1/20 0.34
HSD11B1 P28845 3/20 0.34
SLC6A4 P31645 3/20 0.33
ESR1 P03372 2/20 0.33
ADRA2A P08913 2/20 0.33
ADORA3 P0DMS8 2/20 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 SCHEMBL3689645 0.99 HSD17B10 (0.34) HSD17B10TSHRRARBALDH1A1MEN1
Hydrochloric Acid SCHEMBL3692543 0.97 HSD17B10 (0.32) HSD17B10TSHRRARBALDH1A1MEN1
Hydrochloric Acid SCHEMBL3689637 0.97 HSD17B10 (0.34) HSD17B10TSHRRARBALDH1A1MEN1
Hydrochloric Acid SCHEMBL3687086 0.96 HSD11B1 (0.32) RARBHSD11B1
Hydrochloric Acid SCHEMBL3697200 0.91 GCGR (0.32)
Hydrochloric Acid SCHEMBL3688616 0.91 DHFR (0.34)
Hydrochloric Acid SCHEMBL3687038 0.89 GCGR (0.31)
Hydrochloric Acid SCHEMBL3691143 0.89
Hydrochloric Acid SCHEMBL3686424 0.87
Hydrochloric Acid SCHEMBL7706379 0.86 BCHE (0.31) ACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100056737-A1 Process for manufacturing high to ultra high molecular weight polymers using novel bridged metallocene catalysts NUTRINOVA NUTRITION SPECIALTIES & FOOD INGREDIENTS GMBH (DE) 2010-03-04 US disclosed
US-20070105712-A1 Process for manufacturing ultra high molecular weight polymers using novel bridged metallocene catalysts NUTRINOVA NUTRITION SPECIALTIES & FOOD INGREDIENTS GMBH (DE) 2007-05-10 US disclosed