Hydrochloric Acid

Hydrochloric Acid

SCHEMBL133091

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

nearest known ligand 0.52

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 2/20 0.36
SLC7A5 Q01650 1/20 0.52
ALOX15 P16050 1/20 0.41
SLC1A3 P43003 1/20 0.41
SLC1A2 P43004 1/20 0.41
ANPEP P15144 5/20 0.39
RNPEP Q9H4A4 2/20 0.39
DNPEP Q9ULA0 1/20 0.39
ALDH1A1 P00352 4/20 0.39
METAP2 P50579 1/20 0.37
METAP1 P53582 1/20 0.37
LMNA P02545 1/20 0.37
HSD17B10 Q99714 1/20 0.37
PPID Q08752 1/20 0.37
CYP2D6 P10635 1/20 0.36
CYP2C9 P11712 1/20 0.36
CYP2C19 P33261 1/20 0.36
POLB P06746 2/20 0.36
SMN1; SMN2 Q16637 2/20 0.36
MGAM O43451 1/20 0.36

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 SCHEMBL10887590 1.00 SLC7A5 (0.52) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
Hydrochloric Acid SCHEMBL818970 1.00 SLC7A5 (0.52) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
SCHEMBL133092 0.98 SLC7A5 (0.54) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
SCHEMBL196637 0.98 SLC7A5 (0.54) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
SCHEMBL839402 0.98 SLC7A5 (0.54) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
Hydrochloric Acid SCHEMBL6846663 0.94 SLC7A5 (0.50) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
SCHEMBL10866196 0.92 SLC7A5 (0.48) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
Phosphoric Acid SCHEMBL28734810 0.90 SLC7A5 (0.47) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
Sulfuric Acid SCHEMBL28734782 0.90 SLC7A5 (0.47) SLC7A5ALOX15SLC1A3SLC1A2ANPEP
SCHEMBL28856635 0.88 SLC7A5 (0.45) SLC7A5ALOX15SLC1A3SLC1A2ANPEP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122056386-A Moisture absorption resistant slow release microcapsule powder and preparation method and application thereof 大连医诺生物股份有限公司 2026-05-19 CN claimed
CN-122030612-A Shear-resistant slow-release microcapsule powder and preparation method and application thereof 大连医诺生物股份有限公司 2026-05-15 CN claimed
US-12623994-B2 Method of preparing heterogeneous linear carbonate using catalyst having excellent solubility LOTTE CHEMICAL CORPORATION (KR) 2026-05-12 US claimed
CN-117897386-A Benzopyran derivatives and uses thereof 斯帕克生物制药有限公司 2024-04-16 CN claimed
US-11925644-B2 Crystalline salts of 5-methyl-(6S)-tetrahydrofolic acid and l-leucine ethyl ester MERCK PATENT GMBH (DE) 2024-03-12 US claimed
US-20240002329-A1 METHOD OF PREPARING HETEROGENEOUS LINEAR CARBONATE USING CATALYST HAVING EXCELLENT SOLUBILITY LOTTE CHEMICAL CORPORATION (KR) 2024-01-04 US claimed
EP-4253363-A1 METHOD FOR PRODUCING HETEROGENEOUS LINEAR CARBONATES USING CATALYST WITH EXCELLENT SOLUBILITY Lotte Chemical Corporation (KR) 2023-10-04 EP claimed
EP-3817813-B1 CRYSTALLINE SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND L-LEUCINE ETHYL ESTER MERCK PATENT GMBH (DE) 2023-09-20 EP claimed
CN-116710426-A Method for preparing heterogeneous linear carbonate by using catalyst with excellent solubility 乐天化学株式会社 2023-09-05 CN claimed
WO-2023277656-A1 NOVEL BENZOPYRAN DERIVATIVE AND USE THEREOF (주)스파크바이오파마 2023-01-05 WO claimed
CN-114456108-A N-amino acid ethyl ester nicotinamide and preparation method and application thereof 珀莱雅化妆品股份有限公司 2022-05-10 CN claimed
US-20210283136-A1 CRYSTALLINE SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND L-LEUCINE ETHYL ESTER MERCK PATENT GMBH (DE) 2021-09-16 US claimed
CN-112979485-A Application of 3A type molecular sieve in synthesis of N- (4-acetylene benzene carbonyl) amino acid ester 齐鲁工业大学 2021-06-18 CN claimed
EP-3817813-A1 CRYSTALLINE SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND L-LEUCINE ETHYL ESTER Merck Patent GmbH (DE) 2021-05-12 EP claimed
CN-112312968-A Crystalline salts of 5-methyl- (6S) -tetrahydrofolic acid and ethyl L-leucine 默克专利股份有限公司 2021-02-02 CN claimed
WO-2020007839-A1 CRYSTALLINE SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND L-LEUCINE ETHYL ESTER MERCK PATENT GMBH (DE) 2020-01-09 WO 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
CN-102388017-A A method of synthesising an amino acid derivative of azelaic acid MALAYSIAN PALM OIL BOARD 2012-03-21 CN claimed
WO-2010117258-A1 A METHOD OF SYNTHESISING AN AMINO ACID DERIVATIVE OF AZELAIC ACID MALAYSIAN PALM OIL BOARD (MY) 2010-10-14 WO 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-12623994-B2 Method of preparing heterogeneous linear carbonate using catalyst having excellent solubility MLEC, MSMO1, ADH1C GAA 1849/4885SLC7A5 1046/4885ALOX15 802/4885

“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.