Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6820641

Cl.N.c1ccc2c(c1)CC2

nearest known ligand 0.62

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
HTR2C known ✓ P28335 1/20 0.53
MAOB known ✓ P27338 3/20 0.48
MAOA known ✓ P21397 2/20 0.48
DRD2 known ✓ P14416 1/20 0.43
DRD1 known ✓ P21728 1/20 0.43
DRD4 known ✓ P21917 1/20 0.43
DRD3 known ✓ P35462 1/20 0.43
RET known ✓ P07949 1/20 0.40
HTR2A known ✓ P28223 1/20 0.40
MAPK14 known ✓ Q16539 1/20 0.40
TSHR P16473 1/20 0.62
CYP2A6 P11509 1/20 0.52
CES1 P23141 1/20 0.48
ORAI1 Q96D31 1/20 0.46
ORAI2 Q96SN7 1/20 0.46
ORAI3 Q9BRQ5 1/20 0.46
PNMT P11086 1/20 0.46
CD44 P16070 1/20 0.46
DRD5 P21918 1/20 0.43
PLAU P00749 1/20 0.42

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 SCHEMBL28647349 0.96
Ammonia Solution, Strong SCHEMBL330529 0.96
Hydrochloric Acid SCHEMBL21176564 0.96 TSHR (0.67) TSHRHTR2CCYP2A6MAOBMAOA
Bromide SCHEMBL28479076 0.92 TSHR (0.62) TSHRHTR2CCYP2A6MAOBMAOA
Iodide SCHEMBL29238184 0.92 TSHR (0.62) TSHRHTR2CCYP2A6MAOBMAOA
SCHEMBL29351986 0.92
SCHEMBL4465325 0.92 TSHR (0.71) TSHRHTR2CCYP2A6MAOBMAOA
SCHEMBL34906 0.92
SCHEMBL33555 0.92
Bromide SCHEMBL917076 0.88

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120091702-A Perovskite solar cell based on co-self-assembled molecule induced interface in-situ polymerization and preparation method thereof 南方科技大学 2025-06-03 CN claimed
CN-119907614-A Perovskite precursor solution, perovskite thin film, preparation method of perovskite thin film, photoelectric device and electricity utilization device 天合光能股份有限公司 2025-04-29 CN claimed
CN-222424622-U Perovskite solar cell and electricity utilization device 天合光能股份有限公司 2025-01-28 CN claimed
CN-118338747-A Solar cell and preparation method thereof 天合光能股份有限公司 2024-07-12 CN claimed
CN-118302015-A Perovskite layer preparation method, perovskite battery, perovskite layer preparation method and electricity utilization device 天合光能股份有限公司 2024-07-05 CN claimed
US-12024648-B2 Graphene anti-corrosion coating TORAY INDUSTRIES, INC. (JP) 2024-07-02 US claimed
CN-117700964-A Environment-friendly degradable composite material 昕亮科技(深圳)有限公司 2024-03-15 CN claimed
CN-117417628-A Heat-resistant degradable plastic and preparation method thereof 昕亮科技(深圳)有限公司 2024-01-19 CN claimed
CN-113039251-B Graphene anticorrosive paint 东丽先端材料研究开发(中国)有限公司 2022-09-09 CN claimed
US-20210395536-A1 GRAPHENE ANTI-CORROSION COATING TORAY INDUSTRIES, INC. (JP) 2021-12-23 US claimed
EP-3889224-A1 GRAPHENE ANTI-CORROSION COATING Toray Industries, Inc. (JP) 2021-10-06 EP claimed
CN-113039251-A Graphene anticorrosive paint 东丽先端材料研究开发(中国)有限公司 2021-06-25 CN claimed
CN-107400070-A Biguanides probe and preparation method thereof 清华大学 2017-11-28 CN claimed
CN-120091702-A Perovskite solar cell based on co-self-assembled molecule induced interface in-situ polymerization and preparation method thereof 南方科技大学 2025-06-03 CN disclosed
CN-119907614-A Perovskite precursor solution, perovskite thin film, preparation method of perovskite thin film, photoelectric device and electricity utilization device 天合光能股份有限公司 2025-04-29 CN disclosed
CN-119789742-A Perovskite solar cell based on perovskite thin film crystallization control and preparation method 西安交通大学 2025-04-08 CN disclosed
CN-107400070-A Biguanides probe and preparation method thereof 清华大学 2017-11-28 CN disclosed
US-20040006081-A1 Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity ASTRAZENECA AB (SE) 2004-01-08 US disclosed
EP-1289957-A1 PHARMACEUTICALLY ACTIVE PIPERIDINE DERIVATIVES, IN PARTICULAR AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY AstraZeneca AB (SE) 2003-03-12 EP disclosed
WO-2001087839-A1 PHARMACEUTICALLY ACTIVE PIPERIDINE DERIVATIVES, IN PARTICULAR AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY ASTRAZENECA AB (SE) 2001-11-22 WO 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-20040006081-A1 Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity CCR5, CCR2, CCR1 HTR2C 799/4885MAOB 2844/4885MAOA 3065/4885

“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.