Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4729182

Cl.c1ccc(C[PH](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.41

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
MAOB known ✓ P27338 2/20 0.36
MAOA known ✓ P21397 1/20 0.36
HTR2A known ✓ P28223 1/20 0.35
CALM1 P0DP23 1/20 0.41
TSHR P16473 3/20 0.38
ALDH1A1 P00352 3/20 0.38
LOXL2 Q9Y4K0 2/20 0.38
TRPA1 O75762 2/20 0.38
IDO1 P14902 1/20 0.38
TP53 P04637 1/20 0.38
CYP3A4 P08684 3/20 0.37
MAPT P10636 2/20 0.37
AGXT P21549 1/20 0.37
KDM4E B2RXH2 1/20 0.37
HPGD P15428 2/20 0.36
ALOX15 P16050 1/20 0.36
ALOX12 P18054 1/20 0.36
CASP1 P29466 1/20 0.36
HSD17B10 Q99714 1/20 0.36
TDP1 Q9NUW8 2/20 0.35

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 SCHEMBL15281958 1.00 CALM1 (0.41) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL28147023 1.00 CALM1 (0.41) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL27999670 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL28828300 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL28207048 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL27993384 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL27993655 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL27714197 0.97 CALM1 (0.39) CALM1TSHRALDH1A1LOXL2TRPA1
SCHEMBL122055 0.97 CALM1 (0.43) CALM1TSHRALDH1A1LOXL2TRPA1
Hydrochloric Acid SCHEMBL9312565 0.95 MAOB (0.36) CALM1TSHRALDH1A1LOXL2TRPA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120059469-A High-low temperature-resistant wear-resistant tearing-resistant fluorosilicone rubber compound and preparation method thereof 广东京汕密封件有限公司 2025-05-30 CN claimed
CN-119912741-A High-temperature-resistant rubber emulsion and preparation method and application thereof 河北昊泽化工有限公司 2025-05-02 CN claimed
CN-119639154-A Fluororubber composition 安徽鼎连高分子材料科技有限公司 2025-03-18 CN claimed
CN-119504697-A Cyclohexadiene derivative and preparation method thereof 博璞诺(上海)医药科技发展有限公司 2025-02-25 CN claimed
CN-115960332-B Hexamethylene diisocyanate composition and preparation method and application thereof 万华化学集团股份有限公司 2025-02-18 CN claimed
CN-119371943-A 2-Methyl-1, 3-propanediol-based antifreeze fluid and preparation method thereof 沧州市天津工业大学研究院 2025-01-28 CN claimed
CN-118930945-A Microcellular fluoroelastomer compositions and methods of making the same 上海森桓新材料科技有限公司 2024-11-12 CN claimed
CN-118834483-A Low-temperature-resistant fluororubber sealing material and preparation method thereof 安徽同丰橡塑工业有限公司 2024-10-25 CN claimed
CN-118772557-A Method for preparing sealing ring from perfluoro ether elastomer rubber compound 上海森桓新材料科技有限公司 2024-10-15 CN claimed
CN-118667270-A Aging-resistant fluororubber material with low compression set rate and preparation method and application thereof 四川道弘新材料股份有限公司 2024-09-20 CN claimed
CN-114214647-A Method for synthesizing vitamin A acetate through electrochemical catalysis 万华化学集团股份有限公司 2022-03-22 CN claimed
CN-113546679-A Ionic liquid-ruthenium-based catalyst for catalyzing hydrochlorination of acetylene and preparation method and application thereof 石河子大学 2021-10-26 CN claimed
CN-109438903-A A kind of fire-retardant SBS composite material 俞虹 2019-03-08 CN claimed
CN-108467612-A A kind of environment-friendly water-based paint 甘庆文 2018-08-31 CN claimed
CN-108102259-A A kind of fluorubber and preparation method thereof 沈阳赛亚橡胶制品有限公司 2018-06-01 CN claimed
CN-107474692-A A kind of coating on hollow copper tubing inwall and preparation method thereof 巢湖鹏远金属焊管有限公司 2017-12-15 CN claimed
CN-106349706-A Silicone rubber cable sheath material with high flame resistance 安徽蓝德集团股份有限公司 2017-01-25 CN claimed
US-9522915-B2 Method for preparing an important intermediate of linagliptin 2Y-CHEM, LTD. (CN) 2016-12-20 US claimed
CN-105733050-A Heat-resistant, oil-resistant and anti-flaming modified nitrile butadiene rubber composite 合肥市再德高分子材料有限公司 2016-07-06 CN claimed
US-20150274728-A1 METHOD FOR PREPARING AN IMPORTANT INTERMEDIATE OF LINAGLIPTIN 2Y-CHEM, LTD. (CN) 2015-10-01 US claimed

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-20150274728-A1 METHOD FOR PREPARING AN IMPORTANT INTERMEDIATE OF LINAGLIPTIN DPP4, DPP9, DPP3 MAOB 2912/4885MAOA 2726/4885HTR2A 2231/4885

“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.