Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1893246

C=CC[Al](CC=C)CC=C.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 6)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.35
TRPA1 O75762 2/20 0.35
CYP3A4 P08684 2/20 0.35
HPGD P15428 2/20 0.35
ALOX15 P16050 1/20 0.35
TSHR P16473 2/20 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 SCHEMBL28468211 1.00 ALDH1A1 (0.35) ALDH1A1TRPA1CYP3A4HPGDALOX15
SCHEMBL20950 0.96 ALDH1A1 (0.38) ALDH1A1TRPA1CYP3A4HPGDALOX15
SCHEMBL633460 0.92 ALDH1A1 (0.35) ALDH1A1TRPA1CYP3A4HPGDALOX15
SCHEMBL9643688 0.92 ALDH1A1 (0.35) ALDH1A1TRPA1CYP3A4HPGDALOX15
SCHEMBL8584559 0.92 ALDH1A1 (0.35) ALDH1A1TRPA1CYP3A4HPGDALOX15
Water SCHEMBL31312804 0.92 ALDH1A1 (0.35) ALDH1A1TRPA1CYP3A4HPGDALOX15
Hydrochloric Acid SCHEMBL27797261 0.88 TRPA1 (0.33) ALDH1A1TRPA1CYP3A4HPGDALOX15
Hydrochloric Acid SCHEMBL7858247 0.88 TRPA1 (0.33) ALDH1A1TRPA1CYP3A4HPGDALOX15
SCHEMBL11884168 0.79
SCHEMBL28149750 0.79 TSHR (0.33) ALDH1A1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0358264-B1 Catalyst component and catalyst for the production of very high molecular weight polyolefins ENICHEM SPA (IT) 1994-10-12 EP claimed
CN-117327229-A Modified starch copolymer and preparation method and application thereof 中国石油化工股份有限公司 2024-01-02 CN disclosed
US-9394388-B2 Hybrid supported metallocene catalyst, method for preparing the same, and process for preparing polyolefin using the same SK INNOVATION CO., LTD. (KR) 2016-07-19 US disclosed
CN-105086004-A STUDLESS WINTER TIRE SUMITOMO RUBBER IND 2015-11-25 CN disclosed
US-20150025204-A1 Hybrid Supported Metallocene Catalyst, Method for Preparing the Same, and Process for Preparing Polyolefin Using the Same SK INNOVATION CO., LTD. (KR) 2015-01-22 US disclosed
WO-2013133595-A1 HYBRID SUPPORTED METALLOCENE CATALYST, METHOD FOR PREPARING THE SAME, AND PROCESS FOR PREPARING POLYOLEFIN USING THE SAME SK INNOVATION CO., LTD. (KR) 2013-09-12 WO disclosed
US-8399375-B2 Supported metallocene catalyst composition and a process for the preparation of polyolefin using the same SK GLOBAL CHEMICAL CO., LTD. (KR) 2013-03-19 US disclosed
US-20110105705-A1 Metallocene Supported Catalyst Composition and a Process for the Preparation of Polyolefin Using the Same SK ENERGY CO., LTD. (KR) 2011-05-05 US disclosed
EP-2258731-A2 METALLOCENE SUPPORTED CATALYST COMPOSITION AND A PROCESS FOR THE PREPARATION OF POLYOLEFIN USING THE SAME SK Energy Co., Ltd. (KR) 2010-12-08 EP disclosed
WO-2002074821-A1 A POLY(VINYL CHLORIDE)-g-POLY(α-METHYLSTYRENE) HAVING A SINGLE GLASS TRANSITION TEMPERATURE UNIVERSITY OF AKRON, AKRON OHIO (US) 2002-09-26 WO disclosed
US-6384147-B1 USED AS COMPATIBILIZING AGENT OR AS HIGH HEAT DISTORTION POLYVINYL CHLORIDE MATERIAL UNIVERSITY OF AKRON 2002-05-07 US disclosed