Hydrochloric Acid

Hydrochloric Acid

SCHEMBL569999

CCOC(=O)C(N)CCCNC(=N)N.Cl.Cl

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 13)

geneUniProtsupporting neighboursconfidence
RRM1 known ✓ P23921 1/20 0.36
DPP7 Q9UHL4 2/20 0.41
NOD1 Q9Y239 3/20 0.39
NPY4R P50391 7/20 0.39
NPY1R P25929 5/20 0.39
GNAI3 P08754 1/20 0.37
GNAO1 P09471 1/20 0.37
GNAI1 P63096 1/20 0.37
NPY2R P49146 4/20 0.36
NPY5R Q15761 4/20 0.36
OTC P00480 1/20 0.35
ALOX15 P16050 2/20 0.34
TSHR P16473 1/20 0.33

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 SCHEMBL22411245 1.00 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
Hydrochloric Acid SCHEMBL2897702 1.00 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
Hydrochloric Acid SCHEMBL1487716 1.00 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
Hydrochloric Acid SCHEMBL570000 1.00 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
SCHEMBL93607 0.98 DPP7 (0.42) DPP7NOD1NPY4RNPY1RGNAI3
SCHEMBL9330200 0.98 DPP7 (0.42) DPP7NOD1NPY4RNPY1RGNAI3
SCHEMBL93606 0.98 DPP7 (0.42) DPP7NOD1NPY4RNPY1RGNAI3
Water SCHEMBL28810239 0.97 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
SCHEMBL31592761 0.97 DPP7 (0.41) DPP7NOD1NPY4RNPY1RGNAI3
Acetic Acid SCHEMBL12077668 0.94 NOD1 (0.40) DPP7NOD1NPY4RNPY1RGNAI3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117362202-A Preparation method and equipment of lauroyl arginine ethyl ester hydrochloride 南通市杰阳生物科技有限公司 2024-01-09 CN claimed
CN-108101812-B Production and purification process of lauroyl arginine ethyl ester hydrochloride 成都傲飞生物化学品有限责任公司 2020-12-25 CN claimed
CN-107400069-B Preparation method of lauroyl arginine ethyl ester hydrochloride 浙江大学 2020-02-21 CN claimed
CN-108101812-A A kind of production purifying process of lauroyl arginine ethyl ester hydrochloride 成都傲飞生物化学品有限责任公司 2018-06-01 CN claimed
CN-107400069-A A kind of preparation method of lauroyl arginine ethyl ester hydrochloride 浙江大学 2017-11-28 CN claimed
EP-3010537-A2 Methods for the prevention of aggregation of viral components De Staat der Nederlanden, vert. door de minister Van VWS, Ministerie van Volksgezondheid, Welzijn en Sport (NL) 2016-04-27 EP claimed
WO-2014204303-A2 Methods for the prevention of aggregation of viral components DE STAAT DER NEDERLANDEN, VERT. DOOR DE MINISTER VAN VWS, MINISTERIE VAN VOLKSGEZONDHEID, WELZIJN EN SPORT (NL) 2014-12-24 WO claimed
WO-2003056002-A1 IMPROVEMENT IN AMYLASE STABILITY UNISEARCH LIMITED (AU) 2003-07-10 WO claimed
WO-2003056001-A1 MODIFIED ENZYMES AND MODIFICATION PROCESSES UNISEARCH (AU) 2003-07-10 WO claimed
WO-2003056000-A1 MODIFIED ENZYME AND MODIFICATION PROCESS UNISEARCH (AU) 2003-07-10 WO claimed
US-5780658-A Process for the synthesis of cationic surfactants comprising esterification with basic character amino acids LABORATORIOS MIRET, S.A. (ES) 1998-07-14 US claimed
CN-1091952-A Cosmetic composition UNILEVER NV (NL) 1994-09-14 CN claimed
US-12472448-B2 Compact hydroxamate-based affinity tags for artificially tagging biological macromolecules THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2025-11-18 US disclosed
US-12030850-B2 Method for producing ester based on eco-friendly and high-efficiency esterification by using base exchange of salt and the compound thereof WOODWARD BIO CORP. (KR) 2024-07-09 US disclosed
CN-117362202-A Preparation method and equipment of lauroyl arginine ethyl ester hydrochloride 南通市杰阳生物科技有限公司 2024-01-09 CN disclosed
CN-117362202-A Preparation method and equipment of lauroyl arginine ethyl ester hydrochloride 南通市杰阳生物科技有限公司 2024-01-09 CN disclosed
WO-1996038460-A1 PALLADIUM CATALYZED NUCLEOSIDE MODIFICATION METHODS USING NUCLEOPHILES AND CARBON MONOXIDE NEXSTAR PHARMACEUTICALS, INC. (US) 1996-12-05 WO disclosed
EP-0666729-A1 COSMETIC COMPOSITION UNILEVER PLC (GB) 1995-08-16 EP disclosed
CN-1091952-A Cosmetic composition UNILEVER NV (NL) 1994-09-14 CN disclosed
WO-1994009750-A1 COSMETIC COMPOSITION UNILEVER PLC (GB) 1994-05-11 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 (2 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-12030850-B2 Method for producing ester based on eco-friendly and high-efficiency esterification by using base exchange of salt and the compound thereof SLC6A9, TST, SLC6A5 RRM1 1072/4885DPP7 1954/4885NOD1 2669/4885
US-12472448-B2 Compact hydroxamate-based affinity tags for artificially tagging biological macromolecules HLCS, AADAC, HYPK RRM1 3618/4885DPP7 2140/4885NOD1 2584/4885

“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.