Hydrochloric Acid

Hydrochloric Acid

SCHEMBL374326

CCCCCCCCCCCCCCCCCN.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 2/20 0.57
DNM1 Q05193 9/20 1.00
TSHR P16473 3/20 0.93
MEN1 O00255 1/20 0.93
KMT2A Q03164 1/20 0.93
ALDH1A1 P00352 1/20 0.93
EPHX1 P07099 1/20 0.93
CA12 O43570 2/20 0.57
CA1 P00915 2/20 0.57
CA3 P07451 2/20 0.57
CA4 P22748 2/20 0.57
CA6 P23280 2/20 0.57
CA5A P35218 2/20 0.57
CA7 P43166 2/20 0.57
CA9 Q16790 2/20 0.57
CA14 Q9ULX7 2/20 0.57
CA5B Q9Y2D0 2/20 0.57
THRB P10828 1/20 0.57
LMNA P02545 1/20 0.57
BLM P54132 1/20 0.57

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
Tetradecylamine SCHEMBL93411 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL608566 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL5058635 1.00
Hydrochloric Acid SCHEMBL21590116 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hexadecylamine SCHEMBL21681763 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL23420707 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Octadecylamine SCHEMBL22436607 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL21494288 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Octadecylamine SCHEMBL22436608 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL909627 1.00 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120189885-A Preparation method of multi-chamber microcapsule 广西大学 2025-06-24 CN claimed
CN-112957282-A Oil removing composition for pets and application thereof 小佩网络科技(上海)有限公司 2021-06-15 CN claimed
CN-109646352-A A kind of hair-washing composition with anti-dandruff performance containing pomegranate rind extract 澳宝化妆品(惠州)有限公司 2019-04-19 CN claimed
CN-108584928-A A kind of preparation method of graphene heat conducting film 谢新昇 2018-09-28 CN claimed
CN-106046972-A Preparation method of wear-resistant corrosion-resistant water cooling tank 滁州帝邦科技有限公司 2016-10-26 CN claimed
CN-106048592-A Method of producing corrosion-resistant water-cooling tank 滁州帝邦科技有限公司 2016-10-26 CN claimed
EP-2198708-B1 Window sticker for attracting and killing insects LOHMANN THERAPIE SYST LTS (DE) 2012-04-25 EP claimed
US-20100158965-A1 WINDOW STICKER FOR ATTRACTING AND DESTROYING INSECTS ICS INNOVATIVE CARE SYSTEMS ANDERNACH GMBH (DE) 2010-06-24 US claimed
US-7198888-B2 Water-soluble material, chemically amplified resist and pattern formation method using the same MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2007-04-03 US claimed
US-7147843-B2 Hydrophobic polyether urethane C23+ endcapped (especially from 2-decyltetradecanol) and cationic surfactant; also cleaning agent containing the modified polymer and anionic surfactant and/or ampholytic surfactant. SHISEIDO COMPANY, LTD. (JP) 2006-12-12 US claimed
US-20050158672-A1 Pattern formation method MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. 2005-07-21 US claimed
EP-1553454-A2 Pattern formation method MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2005-07-13 EP claimed
EP-1553453-A2 Water-soluble material, chemically amplified resist and pattern formation method using the same MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2005-07-13 EP claimed
US-20050130079-A1 Pattern formation method MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. 2005-06-16 US claimed
EP-0124200-B1 HEPARINIZATION OF PLASMA TREATED SUBSTRATES Becton Dickinson and Company (US) 1990-06-13 EP claimed
US-4740420-A WATER-SOLUBLE METAL SALT WITH THE ION VALENCE OF METAL BEING 2 TO 4 AND CATIONIC ORGANIC MATERIAL RICOH COMPANY, LTD. (JP) 1988-04-26 US claimed
US-4613517-A CATIONIC SURFACTANT, POLYMERS, MEDICAL EQUIPMENT, REDUCED THROMBOGENICITY BECTON, DICKINSON AND COMPANY (US) 1986-09-23 US claimed
EP-0124200-A2 Heparinization of plasma treated substrates Becton Dickinson and Company (US) 1984-11-07 EP claimed
US-4349467-A HEPARIN SUBSTRATES WILLIAMS JOEL L 1982-09-14 US claimed
US-4302368-A AMINE SALT OF HEPARIN AFFIXED TO POLYMER BECTON, DICKINSON AND COMPANY (US) 1981-11-24 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-20100158965-A1 WINDOW STICKER FOR ATTRACTING AND DESTROYING INSECTS SERBP1, SERPINA6, ADAM17 CA2 1119/4885DNM1 3746/4885TSHR 4032/4885

“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.