Hydrochloric Acid

Hydrochloric Acid

SCHEMBL538996

CCOC(=O)[C@H](CCCNC(=N)N)NC(=O)c1ccccc1.Cl

nearest known ligand 0.47

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
BCHE known ✓ P06276 2/20 0.46
ACHE known ✓ P22303 2/20 0.46
PDE4A known ✓ P27815 3/20 0.45
PDE4B known ✓ Q07343 2/20 0.45
PDE4C known ✓ Q08493 2/20 0.45
PDE4D known ✓ Q08499 2/20 0.45
CA2 known ✓ P00918 1/20 0.45
GRIN1 known ✓ Q05586 1/20 0.41
GRIN2A known ✓ Q12879 1/20 0.41
P2RY12 known ✓ Q9H244 1/20 0.40
CYP26A1 O43174 1/20 0.45
PADI1 Q9ULC6 4/20 0.45
PADI4 Q9UM07 4/20 0.45
PADI2 Q9Y2J8 3/20 0.45
PADI3 Q9ULW8 3/20 0.45
PADI6 Q6TGC4 1/20 0.45
CA1 P00915 1/20 0.45
NAAA Q02083 1/20 0.41
CTSL P07711 1/20 0.40
KDM4E B2RXH2 1/20 0.40

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 SCHEMBL11325263 1.00 BCHE (0.46) BCHEACHECYP26A1PADI1PADI4
SCHEMBL80453 0.99 BCHE (0.47) BCHEACHECYP26A1PADI1PADI4
SCHEMBL562113 0.99 BCHE (0.47) BCHEACHECYP26A1PADI1PADI4
SCHEMBL15739025 0.98 BCHE (0.46) BCHEACHECYP26A1PADI1PADI4
Hydrochloric Acid SCHEMBL29401063 0.91 CA1 (0.53) CYP26A1PADI1PADI4PDE4APADI2
SCHEMBL158087 0.90 CA1 (0.54) CYP26A1PADI1PADI4PDE4APADI2
SCHEMBL31206858 0.90 CA1 (0.54) CYP26A1PADI1PADI4PDE4APADI2
SCHEMBL16289858 0.90 CA1 (0.54) CYP26A1PADI1PADI4PDE4APADI2
SCHEMBL1396385 0.90 BCHE (0.48) BCHEACHECYP26A1PADI1PADI4
SCHEMBL15271466 0.90 BCHE (0.48) BCHEACHECYP26A1PADI1PADI4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119604537-A Antibodies that bind to human PAD4 and uses thereof 百时美施贵宝公司 2025-03-11 CN claimed
CN-118285483-A Rolling and kneading raw meat product production method 山东中粹生态发展有限公司 2024-07-05 CN claimed
CN-116606904-A Method for improving stability of trypsin titer determination result for injection 中国食品药品检定研究院 2023-08-18 CN claimed
CN-110112512-B Totally-enclosed metal-carbon dioxide battery and preparation method thereof 上海大学 2022-10-11 CN claimed
CN-111760473-A Composite semipermeable membrane, preparation method and application 中国石油化工股份有限公司 2020-10-13 CN claimed
CN-111760472-A Composite membrane and preparation method and application thereof 中国石油化工股份有限公司 2020-10-13 CN claimed
CN-111004832-A Method for detecting kallidinogenase 常州千红生化制药股份有限公司 2020-04-14 CN claimed
CN-110112512-A Totally enclosed type metal-carbon dioxide battery and preparation method thereof 上海大学 2019-08-09 CN claimed
CN-107484895-A A kind of just term milch goat special feed and preparation method thereof 山东阳春羊奶乳业有限公司 2017-12-19 CN claimed
CN-102732548-A Establishment and application of wheat germ cell-free protein synthesis system for high level expression of snake venom kininogenase UNIV CHINA AGRICULTURAL 2012-10-17 CN claimed
CN-101407792-B Preparation of pit viper bioactivity enzyme XIUHUA GUO 2010-08-18 CN claimed
CN-101407792-A Preparation of pit viper bioactivity enzyme XIUHUA GUO (CN) 2009-04-15 CN claimed
US-12559570-B2 Anti-PAD2 antibody PHARMA FOODS INTERNATIONAL CO., LTD. (JP) 2026-02-24 US disclosed
US-20250289855-A1 ANTIMICROBIAL CaNCR PEPTIDE FOLDING VARIANTS DONALD DANFORTH PLANT SCIENCE CENTER 2025-09-18 US disclosed
EP-3801068-B1 MODIFIED RAPESEED PROTEIN ISOLATE DSM IP ASSETS BV (NL) 2025-07-30 EP disclosed
EP-4558529-A1 ANTIBODIES BINDING TO HUMAN PAD4 AND USES THEREOF Bristol-Myers Squibb Company (US) 2025-05-28 EP disclosed
US-4246351-A COMPRISING POROUS ADDITION COPOLYMERS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1981-01-20 US disclosed
US-4153687-A Derivatives, having an inhibitory action against protease and an antiphlogistic action, of the trypsin-kallikrein inhibitor obtained from cattle organs (BPTI), their preparation and their use as medicaments BAYER AKTIENGESELLSCHAFT (DE) 1979-05-08 US disclosed
US-4118481-A LYSINE, ARGININE, TYROSINE, PROTEASE INHIBITION BAYER AKTIENGESELLSCHAFT (DE) 1978-10-03 US disclosed
US-3940478-A Proteolytic enzymes as adjuncts to antibiotic prophylaxis of contaminated wounds SUTURES, INC. (US) 1976-02-24 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 (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-12559570-B2 Anti-PAD2 antibody PADI2, PADI1, PADI4 BCHE 2229/4885ACHE 3055/4885PDE4A 727/4885

“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.