Hydrochloric Acid

Hydrochloric Acid

SCHEMBL572907

CCOC(=O)CCCN.Cl

nearest known ligand 0.95

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
PTGS2 known ✓ P35354 1/20 0.52
PDE4D known ✓ Q08499 1/20 0.52
GAA known ✓ P10253 2/20 0.48
GABRP known ✓ O00591 1/20 0.42
GABRD known ✓ O14764 1/20 0.42
HDAC3 known ✓ O15379 1/20 0.42
GABRA1 known ✓ P14867 1/20 0.42
GABRB1 known ✓ P18505 1/20 0.42
GABRG2 known ✓ P18507 1/20 0.42
GABRB3 known ✓ P28472 1/20 0.42
SLC6A1 known ✓ P30531 1/20 0.42
GABRA5 known ✓ P31644 1/20 0.42
GABRA3 known ✓ P34903 1/20 0.42
GABRA2 known ✓ P47869 1/20 0.42
GABRB2 known ✓ P47870 1/20 0.42
GABRA4 known ✓ P48169 1/20 0.42
HDAC4 known ✓ P56524 1/20 0.42
GABRE known ✓ P78334 1/20 0.42
HDAC1 known ✓ Q13547 1/20 0.42
GABRA6 known ✓ Q16445 1/20 0.42

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 SCHEMBL2656136 1.00 CYP1A2 (0.95) CYP1A2NR1I2PGRADORA3PTGS2
SCHEMBL208141 0.98
Water SCHEMBL28807419 0.95 CYP1A2 (0.95) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL3821044 0.93 CYP1A2 (0.83) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL4004213 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL1284223 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL3959012 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL10994303 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL7653012 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2
Hydrochloric Acid SCHEMBL20501205 0.91 CYP1A2 (0.80) CYP1A2NR1I2PGRADORA3PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115245591-B Degradable embolism microsphere and preparation method thereof 苏州浩微生物医疗科技有限公司 2024-06-14 CN claimed
CN-111925298-B 4-CNAB and preparation method thereof 无锡紫杉药业有限公司 2023-05-30 CN claimed
CN-115245591-A Degradable embolism microsphere and preparation method thereof 苏州浩微生物医疗科技有限公司 2022-10-28 CN claimed
CN-114588137-A Application of triclosan in preparation of medicine for killing parasitic nematodes 中国农业科学院兰州兽医研究所 2022-06-07 CN claimed
CN-111333641-B Enhanced fluorescent probe for tetrazine bio-orthogonal labeling and synthesis thereof 中国科学院大连化学物理研究所 2022-05-31 CN claimed
CN-111333645-B Fluorescent probe for marking cytoskeleton 中国科学院大连化学物理研究所 2021-10-15 CN claimed
CN-111925298-A 4-CNAB and preparation method thereof 无锡紫杉药业有限公司 2020-11-13 CN claimed
CN-111333641-A Enhanced fluorescent probe for tetrazine bio-orthogonal labeling and synthesis thereof 中国科学院大连化学物理研究所 2020-06-26 CN claimed
CN-111333645-A Fluorescent probe for marking cytoskeleton 中国科学院大连化学物理研究所 2020-06-26 CN claimed
CN-108864123-B Synthetic method of stemona alkaloid 山西大学 2020-04-17 CN claimed
US-6096124-A Ink compositions XEROX CORPORATION (US) 2000-08-01 US claimed
US-20260078091-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2026-03-19 US disclosed
EP-4694981-A1 HETEROCYCLIC COMPOUNDS AS DUAL INHIBITORS OF PD-L1 AND ADENOSINE RECEPTORS Aurigene Oncology Limited (IN) 2026-02-18 EP disclosed
US-12534452-B2 N-(1H-imidazol-2-yl)benzamide compound and pharmaceutical composition comprising the same as active ingredient KAINOS MEDICINE, INC. (KR) 2026-01-27 US disclosed
EP-4342880-B1 IONIZABLE LIPID COMPOUND FOR NUCLEIC ACID DELIVERY AND LNP COMPOSITION THEREOF JENKEM TECH CO LTD TIANJIN (CN) 2025-09-10 EP disclosed
US-4446113-A HYPOTENSIVE AGENTS BEECHAM GROUP P.L.C. (GB) 1984-05-01 US disclosed
EP-0093535-A1 Novel chromenes and chromans BEECHAM GROUP PLC (GB) 1983-11-09 EP disclosed
EP-0076075-A1 Pharmaceutically active benzopyran compounds BEECHAM GROUP PLC (GB) 1983-04-06 EP disclosed
US-4148998-A ANTIBIOTICS YEDA RESEARCH AND DEVELOPMENT CO., LTD. (IL) 1979-04-10 US disclosed
US-4148798-A ANTIINFLAMMATORY E. R. SQUIBB & SONS, INC. (US) 1979-04-10 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 (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-20260078091-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer TP53, HIF1AN, MDM2 PTGS2 1610/4885PDE4D 1809/4885GAA 3557/4885
US-12534452-B2 N-(1H-imidazol-2-yl)benzamide compound and pharmaceutical composition comprising the same as active ingredient IRAK4, IRAK1, IRAK2 PTGS2 3480/4885PDE4D 2187/4885GAA 2950/4885

“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.