Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7642995

CC(C)=[Zr](C1C=Cc2ccccc21)C1C=Cc2ccccc21.Cl.Cl

nearest known ligand 0.34

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
HTR2A known ✓ P28223 2/20 0.33
HTR6 known ✓ P50406 1/20 0.33
SIGMAR1 known ✓ Q99720 4/20 0.31
CHRM2 known ✓ P08172 1/20 0.31
CHRM1 known ✓ P11229 1/20 0.31
DRD2 known ✓ P14416 1/20 0.31
ADRA2B known ✓ P18089 1/20 0.31
ADRA2C known ✓ P18825 1/20 0.31
CHRM3 known ✓ P20309 1/20 0.31
SLC6A2 known ✓ P23975 1/20 0.31
HTR2C known ✓ P28335 1/20 0.31
ADRA1A known ✓ P35348 1/20 0.31
HRH1 known ✓ P35367 1/20 0.31
DRD3 known ✓ P35462 1/20 0.31
OPRK1 known ✓ P41145 1/20 0.31
HTR2B known ✓ P41595 1/20 0.31
CACNA1B known ✓ Q00975 1/20 0.31
SLC6A3 known ✓ Q01959 1/20 0.31
KCNH2 known ✓ Q12809 1/20 0.31
RET known ✓ P07949 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 SCHEMBL6064765 1.00 BRD4 (0.34) BRD4CCL2HTR2AKDM4EHTR6
SCHEMBL29929995 0.98 BRD4 (0.35) BRD4CCL2HTR2AKDM4EHTR6
SCHEMBL1922929 0.98 BRD4 (0.35) BRD4CCL2HTR2AKDM4EHTR6
SCHEMBL8071475 0.96 BRD4 (0.34) BRD4CCL2HTR2AKDM4EHTR6
Chloromethane SCHEMBL7608709 0.95 BRD4 (0.33) BRD4CCL2HTR2AKDM4EHTR6
Phenol SCHEMBL23273222 0.90 CA12 (0.35) BRD4CCL2HTR2AHTR6SIGMAR1
Hydrochloric Acid SCHEMBL8380981 0.87 POLB (0.33) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL8596413 0.85 POLB (0.33) HTR2AKDM4ELMNATP53CHRM2
Trifluoromethanesulfonic Acid SCHEMBL7681346 0.83 BRD4 (0.31) BRD4CCL2
SCHEMBL5174476 0.78 ALDH1A1 (0.36) KDM4EMEN1KMT2ASMN1; SMN2LMNA

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
US-12398167-B2 Process for producing metallocenes LANXESS ORGANOMETALLICS GMBH (DE) 2025-08-26 US disclosed
EP-3917938-A1 PROCESS FOR PRODUCING METALLOCENES LANXESS Organometallics GmbH (DE) 2021-12-08 EP disclosed
WO-2020156998-A1 PROCESS FOR PRODUCING METALLOCENES LANXESS ORGANOMETALLICS GMBH (DE) 2020-08-06 WO disclosed
EP-3686209-A1 PROCESS FOR PRODUCING METALLOCENES LANXESS Organometallics GmbH (DE) 2020-07-29 EP disclosed
EP-2559714-B1 METHOD FOR PREPARING OLEFIN-DIENE COPOLYMER USING TRANSITION METAL COMPOUND INCLUDING THIOPHENE-CONDENSED RING CYCLOPENTADIENYL LIGAND LOTTE CHEMICAL CORP (KR) 2016-08-10 EP disclosed
EP-2559710-B1 CATALYST COMPOSITION FOR POLYMERIZING OLEFIN AND METHOD FOR PREPARING POLYOLEFIN USING SAME LOTTE CHEMICAL CORP (KR) 2016-07-13 EP disclosed
US-6395846-B1 COORDINATION CATALYST COMPRISING CLAY, ORGANOSILANE COMPOUND, WATER, AND TRANSITION METAL COMPLEX; QUALITY IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-05-28 US disclosed
EP-1026176-A1 CATALYST FOR OLEFIN POLYMER PRODUCTION, PROCESS FOR PRODUCING THE SAME, AND PROCESS FOR PRODUCING OLEFIN POLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2000-08-09 EP disclosed
US-6063880-A VIA SOLUTION, SUSPENSION, OR GAS PHASE HOMO- OR CO-POLYMERIZATION OF OLEFINS OF GIVEN FORMULA IN THE PRESENCE OF A CATALYST CONSISTING OF A METALLOCENE AND ALUMOXANE OF GIVEN FORMULAS; SIMPLIFICATION: NO HYDROGEN GAS NEEDED TARGOR GMBH (DE) 2000-05-16 US disclosed
US-5962719-A Process for the preparation of a polyolefin wax TARGOR GMBH (DE) 1999-10-05 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 (1 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-12398167-B2 Process for producing metallocenes CYP4F2, PRDX2, PRXL2A HTR2A 3539/4885HTR6 4463/4885SIGMAR1 4239/4885

“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.