Hydrochloric Acid

Hydrochloric Acid

SCHEMBL76740

CC[C@H](C)[C@H](N)C(=O)OC.Cl

nearest known ligand 0.43

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 7)

geneUniProtsupporting neighboursconfidence
DPP4 known ✓ P27487 12/20 0.43
CA2 known ✓ P00918 1/20 0.39
DPP8 Q6V1X1 8/20 0.43
DPP9 Q86TI2 7/20 0.43
IARS1 P41252 3/20 0.41
CA1 P00915 1/20 0.39
DPP7 Q9UHL4 7/20 0.39

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 SCHEMBL4284558 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL76739 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL4284560 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL5420866 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL1599029 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL233325 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
Hydrochloric Acid SCHEMBL31084736 1.00 DPP4 (0.43) DPP4DPP8DPP9IARS1CA1
SCHEMBL76741 0.98 DPP4 (0.44) DPP4DPP8DPP9IARS1CA1
SCHEMBL1770623 0.98 DPP4 (0.44) DPP4DPP8DPP9IARS1CA1
SCHEMBL1770627 0.98 DPP4 (0.44) DPP4DPP8DPP9IARS1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119899137-A Method for preparing Fmoc-Ile-OH by chemical derivatization 杭州湃肽生化科技有限公司 2025-04-29 CN claimed
CN-119874660-A Amino acid derivative-rhodamine B conjugate, preparation method thereof and application thereof as fluorescent tracer 内蒙古农业大学 2025-04-25 CN claimed
CN-119504883-A Synthesis method of RNA monomer intermediate 2' -fluoro-nucleoside modifier 安徽信佰生物医药科技有限公司 2025-02-25 CN claimed
CN-119409588-A Caffeoyl amino acid methyl ester derivative and preparation method and application thereof 西北大学 2025-02-11 CN claimed
CN-119241617-A 2 '-Deoxy-2' -fluoro-N4-substituted cytidine compound, preparation method and application thereof 河南省科学院高新技术研究中心 2025-01-03 CN claimed
CN-117903078-A Amide derivative containing 3, 4-dichloro isothiazole, preparation method and application thereof 南开大学 2024-04-19 CN claimed
CN-116970587-A Alpha-amino acid ester acyltransferase mutant, amino acid sequence and application thereof 大连医诺生物股份有限公司 2023-10-31 CN claimed
CN-113527399-B Ginsenoside CK derivative and application thereof in preparation of antitumor drugs 陕西巨子生物技术有限公司 2023-01-31 CN claimed
CN-113527399-A Ginsenoside CK derivative and application thereof in preparation of antitumor drugs 陕西巨子生物技术有限公司 2021-10-22 CN claimed
CN-109847455-B Composite material for filtering fine particles, preparation method and application thereof 四川大学 2021-07-06 CN claimed
CN-104788537-A Novel tetrapeptide compound as well as preparation method and application thereof CHANGCHUN APPLIED CHEMISTRY 2015-07-22 CN claimed
CN-102432494-B Novel chemical total synthesis preparation method for coronalon SOUTH CHINA BOTAN GARDEN CAS 2013-12-04 CN claimed
CN-102432494-A Novel chemical total synthesis preparation method of Coronalon SOUTH CHINA BOTAN GARDEN CAS 2012-05-02 CN claimed
CN-102262124-A Method for detecting content of L-isoleucine methyl ester hydrochloride 2011-11-30 CN claimed
CN-101560190-B Method for researching and controlling impurity E in Valsartan BEIJING SECOND PHARMACEUTICAL CO LTD 2011-04-27 CN claimed
EP-0397652-B1 WATER INSOLUBLE DERIVATIVES OF HYALURONIC ACID GENZYME CORP (US) 1996-06-05 EP claimed
EP-0397652-A4 WATER INSOLUBLE DERIVATIVES OF HYALURONIC ACID 1991-04-03 EP claimed
EP-0397652-A1 WATER INSOLUBLE DERIVATIVES OF HYALURONIC ACID. GENZYME CORP (US) 1990-11-22 EP claimed
US-4937270-A Water insoluble derivatives of hyaluronic acid GENZYME CORPORATION (US) 1990-06-26 US claimed
WO-1989002445-A1 WATER INSOLUBLE DERIVATIVES OF HYALURONIC ACID GENZYME CORPORATION (US) 1989-03-23 WO claimed