Hydrochloric Acid

Hydrochloric Acid

SCHEMBL138333

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

nearest known ligand 0.44

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
GAA known ✓ P10253 1/20 0.39
ALOX15 P16050 1/20 0.44
SLC7A5 Q01650 1/20 0.44
ALDH1A1 P00352 4/20 0.42
LMNA P02545 1/20 0.40
HSD17B10 Q99714 1/20 0.40
MGAM O43451 1/20 0.39
SI P14410 1/20 0.39
MGAM2 Q2M2H8 1/20 0.39
SOAT1 P35610 1/20 0.39
CYP2D6 P10635 1/20 0.38
CYP2C9 P11712 1/20 0.38
CYP2C19 P33261 1/20 0.38
PIN1 Q13526 1/20 0.37
HPGD P15428 1/20 0.37
METAP2 P50579 3/20 0.37
METAP1 P53582 3/20 0.37
CAD P27708 1/20 0.36
TRPA1 O75762 1/20 0.36
CYP1A2 P05177 1/20 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 SCHEMBL135321 1.00 ALOX15 (0.44) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
Hydrochloric Acid SCHEMBL6389383 1.00 ALOX15 (0.44) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
SCHEMBL6389387 0.98 ALOX15 (0.46) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
SCHEMBL196141 0.98 ALOX15 (0.46) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
SCHEMBL135322 0.98 ALOX15 (0.46) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
SCHEMBL3918851 0.95 ALOX15 (0.44) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
SCHEMBL3918852 0.95 ALOX15 (0.44) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
Hydrochloric Acid SCHEMBL20267442 0.93 ALOX15 (0.42) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
Hydrochloric Acid SCHEMBL6846658 0.93 ALOX15 (0.42) ALOX15SLC7A5ALDH1A1LMNAHSD17B10
Hydrochloric Acid SCHEMBL8848952 0.87 ALOX15 (0.50) ALOX15ALDH1A1LMNAHSD17B10MGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3817814-B1 CRYSTALLINE SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND L-VALINE ETHYL ESTER MERCK PATENT GMBH (DE) 2023-09-20 EP claimed
CN-112876402-A Synthetic method of 5F-EMB-PICA 公安部物证鉴定中心 2021-06-01 CN claimed
EP-3082778-B1 STABLE LIQUID FILLED HARD CAPSULE COMPRISING BETA-HYDROXY-BETA-METHYLBUTYRIC ACID CAPSUGEL BELGIUM NV (BE) 2019-04-03 EP claimed
US-20160296475-A1 STABLE LIQUID FILLED HARD CAPSULE COMPRISING BETA-HYDROXY-BETA METHYLBUTYRIC ACID CAPSUGEL BELGIUM NV (BE) 2016-10-13 US claimed
US-12516037-B2 Substituted thiophenecarboxamides and analogues as antibacterials agents BAYER AKTIENGESELLSCHAFT (DE) 2026-01-06 US disclosed
US-12509437-B2 Substituted thiophene carboxamides and derivatives thereof as microbicides BAYER AKTIENGESELLSCHAFT (DE) 2025-12-30 US disclosed
CN-115087650-B Substituted thiophenecarboxamides and derivatives thereof as microbiocides 拜耳公司 2024-12-06 CN disclosed
US-20240360098-A1 SUBSTITUTED THIOPHENECARBOXAMIDES AND ANALOGUES AS ANTIBACTERIALS AGENTS BAYER AKTIENGESELLSCHAFT (DE) 2024-10-31 US disclosed
CN-118580159-A Synthesis method of nitrogen heterocyclic aromatic hydrocarbon modified beta-amino acid ester 国科大杭州高等研究院 2024-09-03 CN disclosed
EP-4077303-B1 SUBSTITUTED THIOPHENE CARBOXAMIDES AND DERIVATIVES THEREOF AS MICROBIOCIDES BAYER AG (DE) 2024-05-29 EP disclosed
CN-114557401-B Composite microbial feed and preparation method thereof 云南大台农台标农业科技有限公司 2024-04-19 CN disclosed
US-11952359-B2 Substituted thiophenecarboxamides and analogues as antibacterials agents BAYER AKTIENGESELLSCHAFT (DE) 2024-04-09 US disclosed
US-5189205-A Reacting carbon dioxide with a primary amine to form an ammonium carbamate salt; reacting with an electrophilic or oxophilic salt MONSANTO COMPAMY (US) 1993-02-23 US disclosed
US-5112837-A Inhibitors of thymidylate synthetase enzyme IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-05-12 US disclosed
US-4981856-A QUINAZOLINE IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-01-01 US disclosed
EP-0147211-B1 4H-3,1-BENZOXAZIN-4-ONES AND RELATED COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND PROCESSES FOR THEIR PREPARATION SYNTEX (U.S.A.) INC. (US) 1990-09-12 EP disclosed
EP-0318225-A2 6-Aryl aminomethyl quinoline derivatives and their use as anti-tumour agents IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-05-31 EP disclosed
EP-0284338-A2 Anti-tumour agents IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-09-28 EP disclosed
US-4657893-A ANTIINFLAMMATORY AGENTS SYNTEX (U.S.A.) INC. (US) 1987-04-14 US disclosed
EP-0147211-A2 4H-3,1-benzoxazin-4-ones and related compounds, pharmaceutical compositions containing them, and processes for their preparation SYNTEX (U.S.A.) INC. (US) 1985-07-03 EP 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 (3 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-12509437-B2 Substituted thiophene carboxamides and derivatives thereof as microbicides CBR1, CBR3, CCR2 GAA 3334/4885ALOX15 1931/4885SLC7A5 3036/4885
US-20240360098-A1 SUBSTITUTED THIOPHENECARBOXAMIDES AND ANALOGUES AS ANTIBACTERIALS AGENTS TST, TBK1, PGLS GAA 279/4885ALOX15 3155/4885SLC7A5 1257/4885
US-11952359-B2 Substituted thiophenecarboxamides and analogues as antibacterials agents TST, XDH, PGLS GAA 252/4885ALOX15 2228/4885SLC7A5 1141/4885

“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.