Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5153699

CC1=Cc2c(ccc3ccccc23)C1[Zr](C)(C)([SiH3])C1C(C)=Cc2c1ccc1ccccc21.Cl

nearest known ligand 0.35

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
KDM4E B2RXH2 2/20 0.35
ALDH1A1 P00352 4/20 0.35
CYP2A6 P11509 3/20 0.35
TSHR P16473 3/20 0.33
CYP1A2 P05177 2/20 0.33
MAPT P10636 2/20 0.33
ALOX12 P18054 1/20 0.33
HSD17B10 Q99714 4/20 0.33
HPGD P15428 3/20 0.33
TDP1 Q9NUW8 1/20 0.32
POLB P06746 1/20 0.32
CYP3A4 P08684 2/20 0.31
MAPK1 P28482 1/20 0.31
CASP1 P29466 1/20 0.31
RAB9A P51151 1/20 0.31
CASP7 P55210 1/20 0.31
ATM Q13315 1/20 0.31
HIF1A Q16665 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
HPRT1 P00492 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 SCHEMBL6440146 0.86 ALDH1A1 (0.33) KDM4EALDH1A1CYP2A6MAPTALOX12
SCHEMBL7885487 0.81 KDM4E (0.34) KDM4EALDH1A1CYP2A6TSHRCYP1A2
Hydrochloric Acid SCHEMBL7122445 0.76 CYP2A6 (0.33) KDM4EALDH1A1CYP2A6TSHRCYP1A2
SCHEMBL9249191 0.76 ALDH1A1 (0.41) KDM4EALDH1A1CYP2A6TSHRCYP1A2
Hydrochloric Acid SCHEMBL6433747 0.75 PDCD1 (0.32)
Hydrochloric Acid SCHEMBL6064180 0.74 CYP2A6 (0.41) KDM4EALDH1A1CYP2A6TSHRCYP1A2
SCHEMBL3965890 0.74 ALDH1A1 (0.42) KDM4EALDH1A1CYP2A6TSHRCYP1A2
SCHEMBL8673527 0.72 CYP2A6 (0.42) KDM4EALDH1A1CYP2A6TSHRCYP1A2
SCHEMBL6244475 0.72 ALDH1A1 (0.37) KDM4EALDH1A1CYP2A6TSHRCYP1A2
Hydrochloric Acid SCHEMBL271719 0.71 CA12 (0.32) KDM4EALDH1A1CYP2A6MAPTALOX12

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
EP-0876405-B2 OLEFIN POLYMERIZATION CATALYST SYSTEM, PRODUCING AND USING IT BOREALIS AS (DK) 2007-01-03 EP disclosed
US-6225423-B1 AS POLYMERIZATION CATALYST USED IN OLEFIN POLYMERIZATION BOREALIS TECHNOLGY OY (FI) 2001-05-01 US disclosed
EP-0876405-B1 OLEFIN POLYMERIZATION CATALYST SYSTEM, PRODUCING AND USING IT BOREALIS AS (DK) 2000-03-15 EP disclosed
EP-0876405-A1 OLEFIN POLYMERIZATION CATALYST SYSTEM, PRODUCING AND USING IT BOREALIS A/S (DK) 1998-11-11 EP disclosed
WO-1997027224-A1 OLEFIN POLYMERIZATION CATALYST SYSTEM, PRODUCING AND USING IT BOREALIS A/S (DK) 1997-07-31 WO disclosed