Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7935735

CC1=C([Ti+2](C)(C)NC(C)(C)C)C(C)c2ccc3c(ccc4ccccc43)c21.[Cl-].[Cl-].[SiH4]

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 15)

geneUniProtsupporting neighboursconfidence
HPRT1 P00492 1/20 0.33
MEN1 O00255 1/20 0.30
USP2 O75604 1/20 0.30
ALDH1A1 P00352 1/20 0.30
LMNA P02545 1/20 0.30
TP53 P04637 1/20 0.30
CYP1A2 P05177 1/20 0.30
CYP2D6 P10635 1/20 0.30
CYP2C9 P11712 1/20 0.30
HPGD P15428 1/20 0.30
ALOX12 P18054 1/20 0.30
MAPK1 P28482 1/20 0.30
CYP2C19 P33261 1/20 0.30
KMT2A Q03164 1/20 0.30
HIF1A Q16665 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
Hydrochloric Acid SCHEMBL7926903 0.76 HPRT1 (0.33) HPRT1
SCHEMBL7926980 0.73 HPRT1 (0.35) HPRT1MEN1USP2ALDH1A1LMNA
SCHEMBL7926994 0.71 HPRT1 (0.35) HPRT1MEN1USP2ALDH1A1LMNA
Hydrochloric Acid SCHEMBL7257433 0.63
Hydrochloric Acid SCHEMBL7173163 0.62
SCHEMBL8740444 0.58 HPRT1 (0.50) HPRT1ALDH1A1CYP1A2HPGDHIF1A
Chrysene SCHEMBL9786466 0.58 HPRT1 (1.00) HPRT1MEN1USP2ALDH1A1LMNA
SCHEMBL25510 0.58 HPRT1 (1.00) HPRT1MEN1USP2ALDH1A1LMNA
Chrysene SCHEMBL384031 0.58 HPRT1 (1.00) HPRT1MEN1USP2ALDH1A1LMNA
Chrysene SCHEMBL27115 0.58 HPRT1 (1.00) HPRT1MEN1USP2ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6329486-B1 PHYSICAL PROPERTIES THE DOW CHEMICAL COMPANY 2001-12-11 US disclosed
US-6323294-B1 CONTACTING C.SUB.2-100,000 OLEFIN/S UNDER POLYMERIZATION CONDITIONS WITH CATALYST SYSTEM COMPRISING METAL COMPLEX AND ACTIVATING COCATALYST OR REACTION PRODUCT OF METAL COMPLEX AND COCATALYST TO FORM ADDITION POLYMER THE DOW CHEMICAL COMPANY 2001-11-27 US disclosed
EP-1017701-A1 CYCLOPENTAPHENANTHRENEYL METAL COMPLEXES AND POLYMERIZATION PROCESS THE DOW CHEMICAL COMPANY (US) 2000-07-12 EP disclosed
WO-1999014221-A1 CYCLOPENTAPHENANTHRENEYL METAL COMPLEXES AND POLYMERIZATION PROCESS THE DOW CHEMICAL COMPANY (US) 1999-03-25 WO disclosed