Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4704089

C=CC[In].C=CC[In].Cl.Cl.Cl

nearest known ligand 0.36

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 8)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.36
ALDH1A1 P00352 2/20 0.36
TRPA1 O75762 1/20 0.31
CYP3A4 P08684 1/20 0.31
HPGD P15428 1/20 0.31
ALOX15 P16050 1/20 0.31
ALOX5 P09917 1/20 0.31
SMN1; SMN2 Q16637 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
SCHEMBL251120 0.95
Bromide SCHEMBL941951 0.90
Hydrochloric Acid SCHEMBL7530764 0.70
Hydrochloric Acid SCHEMBL27275310 0.63
Hydrochloric Acid SCHEMBL29425309 0.63
SCHEMBL546972 0.63
Hydrochloric Acid SCHEMBL7986636 0.60
Hydrochloric Acid SCHEMBL9419899 0.60
Hydrochloric Acid SCHEMBL1486869 0.60
Allyl Alcohol SCHEMBL4601219 0.60

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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3630781-B1 PREPARATION OF TRAIL KYLINDIUM COMPOUNDS IN THE PRESENCE OF CARBOXYLATES UMICORE AG & CO KG (DE) 2021-05-05 EP claimed
EP-3409676-B1 PREPARATION OF TRAIL KYLINDIUM COMPOUNDS IN THE PRESENCE OF CARBOXYLATES UMICORE AG & CO KG (DE) 2020-10-14 EP claimed
CN-105473598-A Method for producing alkyl indium compound and use thereof UMICORE AG & CO KG 2016-04-06 CN claimed
EP-3256478-B1 PROCESS FOR PREPARING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF UMICORE AG & CO KG (DE) 2020-10-28 EP disclosed
US-10745421-B2 Method for producing alkyl-indium compounds and the use thereof UMICORE AG & CO. KG (DE) 2020-08-18 US disclosed
US-10385073-B2 Process for preparing alkyl-indium compounds and the use thereof UMIICORE AG & CO. KG (DE) 2019-08-20 US disclosed
US-10385073-B2 Process for preparing alkyl-indium compounds and the use thereof UMIICORE AG & CO. KG (DE) 2019-08-20 US disclosed
US-20190194229-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF UMICORE AG & CO. KG (DE) 2019-06-27 US disclosed
US-10239892-B2 Method for producing alkyl-indium compounds and the use thereof UMICORE AG & CO. KG (DE) 2019-03-26 US disclosed
CN-105473598-B Method for producing alkyl indium compound and use thereof 优美科股份公司及两合公司 2018-05-08 CN disclosed
EP-3256478-A1 PROCESS FOR PREPARING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF Umicore AG & Co. KG (DE) 2017-12-20 EP disclosed
US-20160207942-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF UMICORE AG & CO. KG (DE) 2016-07-21 US disclosed
EP-3036243-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF Umicore AG & Co. KG (DE) 2016-06-29 EP disclosed
CN-105473598-A Method for producing alkyl indium compound and use thereof UMICORE AG & CO KG 2016-04-06 CN disclosed
CN-105473598-A Method for producing alkyl indium compound and use thereof UMICORE AG & CO KG 2016-04-06 CN disclosed
WO-2015024894-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF UMICORE AG & CO. KG (DE) 2015-02-26 WO disclosed
EP-1643547-B1 Preparation of group 12 and 13 metal compounds having low levels of oxygenated impurities ROHM & HAAS ELECT MAT (US) 2008-11-05 EP disclosed
US-7166734-B2 Method for making organometallic compounds ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) 2007-01-23 US disclosed
EP-1643547-A1 Preparation of group 12 and 13 metal compounds having low levels of oxygenated impurities Rohm and Haas Electronic Materials, L.L.C. (US) 2006-04-05 EP disclosed
US-20060047132-A1 Method ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) 2006-03-02 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10385073-B2 Process for preparing alkyl-indium compounds and the use thereof ENY2, RPS4Y1, RPS4X TSHR 4525/4885ALDH1A1 3475/4885TRPA1 2147/4885
US-20190194229-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF RPS4Y1, ENY2, RPS4X TSHR 4481/4885ALDH1A1 2914/4885TRPA1 2234/4885
US-10239892-B2 Method for producing alkyl-indium compounds and the use thereof RPS4Y1, ENY2, RPS4X TSHR 4375/4885ALDH1A1 2831/4885TRPA1 2013/4885
US-20160207942-A1 METHOD FOR PRODUCING ALKYL-INDIUM COMPOUNDS AND THE USE THEREOF RPS4Y1, ENY2, RPS4X TSHR 4481/4885ALDH1A1 2914/4885TRPA1 2234/4885
US-10745421-B2 Method for producing alkyl-indium compounds and the use thereof RPS4Y1, ENY2, RPS4X TSHR 4481/4885ALDH1A1 2914/4885TRPA1 2234/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.