Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7799642

Cl.c1ccc2c(c1)ccc1[nH]ccc12

nearest known ligand 0.52

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
CA2 known ✓ P00918 1/20 0.48
PARP1 known ✓ P09874 1/20 0.47
ALDH1A1 P00352 4/20 0.52
HSD17B10 Q99714 4/20 0.52
CYP2A6 P11509 1/20 0.52
TSHR P16473 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
AHR P35869 2/20 0.48
TRPA1 O75762 1/20 0.48
CA1 P00915 1/20 0.48
ITGB2 P05107 1/20 0.48
ICAM1 P05362 1/20 0.48
ITGAL P20701 1/20 0.48
CA4 P22748 1/20 0.48
CA6 P23280 1/20 0.48
ADK P55263 1/20 0.48
HPRT1 P00492 1/20 0.48
KDM4E B2RXH2 2/20 0.46
RAB9A P51151 2/20 0.46
SIRT2 Q8IXJ6 1/20 0.46

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
SCHEMBL29628855 0.98 ALDH1A1 (0.55) ALDH1A1HSD17B10CYP2A6TSHRTDP1
SCHEMBL280428 0.98 ALDH1A1 (0.55) ALDH1A1HSD17B10CYP2A6TSHRTDP1
Water SCHEMBL3636507 0.96 ALDH1A1 (0.52) ALDH1A1HSD17B10CYP2A6TSHRTDP1
Iodide SCHEMBL6832071 0.96 ALDH1A1 (0.52) ALDH1A1HSD17B10CYP2A6TSHRTDP1
Bromide SCHEMBL7761036 0.96 ALDH1A1 (0.52) ALDH1A1HSD17B10CYP2A6TSHRTDP1
Water SCHEMBL10356864 0.94 ALDH1A1 (0.50) ALDH1A1HSD17B10CYP2A6TSHRTDP1
SCHEMBL29444130 0.94 HPRT1 (0.58) ALDH1A1HSD17B10CYP2A6TSHRTDP1
Water SCHEMBL10356869 0.94 ALDH1A1 (0.50) ALDH1A1HSD17B10CYP2A6TSHRTDP1
SCHEMBL2126075 0.94 HPRT1 (0.58) ALDH1A1HSD17B10CYP2A6TSHRTDP1
SCHEMBL30713692 0.94 HPRT1 (0.58) ALDH1A1HSD17B10CYP2A6TSHRTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021105888-A1 CRYSTAL OF INDOCYANINE COMPOUND ASTELLAS PHARMA, INC. (JP) 2021-06-03 WO claimed
EP-3120392-A1 TRANSPARENT ENERGY-HARVESTING DEVICES Board of Trustees of Michigan State University (US) 2017-01-25 EP claimed
WO-2015143038-A1 TRANSPARENT ENERGY-HARVESTING DEVICES BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2015-09-24 WO claimed
EP-3857276-A1 TRANSPARENT LUMINESCENT SOLAR CONCENTRATOR Board Of Trustees Of Michigan State University (US) 2021-08-04 EP disclosed
WO-2021105888-A1 CRYSTAL OF INDOCYANINE COMPOUND ASTELLAS PHARMA, INC. (JP) 2021-06-03 WO disclosed
WO-2020068670-A1 TRANSPARENT LUMINESCENT SOLAR CONCENTRATOR BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2020-04-02 WO disclosed
EP-3120392-A1 TRANSPARENT ENERGY-HARVESTING DEVICES Board of Trustees of Michigan State University (US) 2017-01-25 EP disclosed
WO-2015143038-A1 TRANSPARENT ENERGY-HARVESTING DEVICES BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2015-09-24 WO disclosed
EP-1161469-A1 THERMALLY REACTIVE NEAR INFRARED ABSORPTION POLYMER COATINGS, METHOD OF PREPARING AND METHODS OF USE American Dye Source, Inc. (CA) 2001-12-12 EP disclosed
WO-2000056791-A1 THERMALLY REACTIVE NEAR INFRARED ABSORPTION POLYMER COATINGS, METHOD OF PREPARING AND METHODS OF USE AMERICAN DYE SOURCE, INC. (CA) 2000-09-28 WO disclosed