Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5218604

CC1(C)CC(=O)CC(C)(C)N1.Cl

nearest known ligand 0.54

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 11)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.54
ALDH1A1 P00352 2/20 0.44
KDM4E B2RXH2 1/20 0.33
LMNA P02545 1/20 0.33
CYP2C19 P33261 1/20 0.33
TSHR P16473 2/20 0.32
MEN1 O00255 1/20 0.32
MAPK1 P28482 1/20 0.32
KMT2A Q03164 1/20 0.32
NPSR1 Q6W5P4 1/20 0.31
ALOX15 P16050 1/20 0.30

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 SCHEMBL20704047 1.00 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
SCHEMBL38953 0.97 SMN1; SMN2 (0.56) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Ammonia Solution, Strong SCHEMBL27484151 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Iodide SCHEMBL11830139 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Water SCHEMBL7733637 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Water SCHEMBL4837114 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
SCHEMBL29829697 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
SCHEMBL10892597 0.94 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Ethylene SCHEMBL6311271 0.92 SMN1; SMN2 (0.52) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19
Hydrochloric Acid SCHEMBL1572556 0.92 SMN1; SMN2 (0.58) SMN1; SMN2ALDH1A1KDM4ELMNACYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220264914-A1 MATERIALS AND METHODS FOR EXTENDING SHELF-LIFE OF FOODS JP LABORATORIES, INC. 2022-08-25 US claimed
US-20220225647-A1 MATERIALS AND METHODS FOR EXTENDING SHELF-LIFE OF FOODS JP LABORATORIES, INC. 2022-07-21 US claimed
CN-101775057-A Method for preparing drospirenone and intermediate thereof ZHEJIANG XIANJU PHARMACEUTICAL 2010-07-14 CN claimed
JP-56025185-A None JP disclosed
US-20260125363-A1 PROCESSES FOR MAKING MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR VERTEX PHARMA (US) 2026-05-07 US disclosed
US-20260102759-A1 POLYCRYSTALLINE-IRON-LOADED POROUS BIOCHAR AEROGEL CATALYST AND PREPARATION METHOD AND APPLICATION THEREOF UNIV WENZHOU (CN) 2026-04-16 US disclosed
EP-4635513-A1 NEAR-INFRARED PHOTOSENSITIZER THAT CAN BE ACTIVATED IN SLIGHTLY ACIDIC TUMOR ENVIRONMENT AND PREPARATION METHOD THEREFOR AND USE THEREOF Shenzhen University (CN) 2025-10-22 EP disclosed
US-12415798-B2 Processes for making modulators of cystic fibrosis transmembrane conductance regulator VERTEX PHARMACEUTICALS INCORPORATED (US) 2025-09-16 US disclosed
US-20240025877-A1 PROCESSES FOR MAKING MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR VERTEX PHARMACEUTICALS INCORPORATED 2024-01-25 US disclosed
US-11737481-B2 Materials and methods for extending shelf-life of foods JP LABORATORIES, INC. (US) 2023-08-29 US disclosed
US-11465985-B2 Processes for making modulators of cystic fibrosis transmembrane conductance regulator VERTEX PHARMACEUTICALS INCORPORATED (US) 2022-10-11 US disclosed
US-4500663-A Light stabilizing N,N,N-tris(2,2,6,6-tetramethyl-4-piperidone ketal)-1,3,5-triazine derivatives and light stabilized synthetic resin compositions ADEKA ARGUS CHEMICAL CO., LTD. (JP) 1985-02-19 US disclosed
EP-0095571-A2 Polyhydric alcohol ethers of 2,2,6,6-tetramethyl-4-piperidone ketals and synthetic resin compositions ADEKA ARGUS CHEMICAL CO., Ltd. (JP) 1983-12-07 EP disclosed
US-4351915-A OXIDATION AND HEAT RESISTANCE ADEKA ARGUS CHEMICAL CO., LTD. (JP) 1982-09-28 US disclosed
US-4323684-A IN A POLAR SOLVENT ADEKA ARGUS CHEMICAL CO., LTD. 1982-04-06 US disclosed
EP-0045358-A2 2,2,6,6-Tetramethyl-4-piperidyl spiro aliphatic ethers as stabilizers for synthetic polymers ADEKA ARGUS CHEMICAL CO., Ltd. (JP) 1982-02-10 EP disclosed
JP-S5625185-A PREPARATION OF 4-PIPERIDONE SPIROKETAL COMPOUND ADEKA ARGUS CHEM CO LTD 1981-03-10 JP disclosed
US-4251435-A FOR POLYOLEFINS THE B. F. GOODRICH COMPANY (US) 1981-02-17 US disclosed
US-4250313-A HEATING A 2,2,6,6-TETRAMETHYL-4-PIPERIDONE AND A 5-METHYLOL-1,3-DIOXANE ARGUS CHEMICAL CORP. (US) 1981-02-10 US disclosed
US-4173599-A 2,2,6,6-Tetraalkyl-4-piperidyl ketones and ketals as stabilizers for synthetic polymers ARGUS CHEMICAL CORPORATION (US) 1979-11-06 US 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 (5 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-20260125363-A1 PROCESSES FOR MAKING MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR CFTR, SLC26A4, SLC26A3 SMN1; SMN2 2940/4885ALDH1A1 3574/4885KDM4E 1638/4885
US-20240025877-A1 PROCESSES FOR MAKING MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR CFTR, SCNN1B, SCNN1G SMN1; SMN2 4759/4885ALDH1A1 3677/4885KDM4E 4464/4885
US-20260102759-A1 POLYCRYSTALLINE-IRON-LOADED POROUS BIOCHAR AEROGEL CATALYST AND PREPARATION METHOD AND APPLICATION THEREOF FECH, SCO2, TFRC SMN1; SMN2 4408/4885ALDH1A1 4239/4885KDM4E 2654/4885
US-11465985-B2 Processes for making modulators of cystic fibrosis transmembrane conductance regulator CFTR, SCNN1B, SCNN1G SMN1; SMN2 4752/4885ALDH1A1 3381/4885KDM4E 4286/4885
US-12415798-B2 Processes for making modulators of cystic fibrosis transmembrane conductance regulator CFTR, SCNN1B, SCNN1G SMN1; SMN2 4759/4885ALDH1A1 3677/4885KDM4E 4464/4885

“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.