Hydrochloric Acid

Hydrochloric Acid

SCHEMBL25383156

Cl.N[C@H](Cc1ccccc1)[C@H](O)C(=O)NCc1nccs1

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
▸ LAP3 P28838 3/20 0.52
▸ ANPEP P15144 1/20 0.52
▸ RNPEP Q9H4A4 1/20 0.52
▸ DNPEP Q9ULA0 1/20 0.52
▸ PKM P14618 1/20 0.46
▸ KDM4E B2RXH2 1/20 0.45
▸ HSPA1A P0DMV8 1/20 0.45
▸ HSPA5 P11021 1/20 0.45
▸ HSPA9 P38646 1/20 0.45
▸ HSPA2 P54652 1/20 0.45
▸ SMN1; SMN2 Q16637 2/20 0.44
▸ CYP1A2 P05177 1/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ MAPT P10636 1/20 0.44
▸ TSHR P16473 1/20 0.44
▸ LTA4H P09960 2/20 0.41
▸ L3MBTL1 Q9Y468 1/20 0.41
▸ GPR88 Q9GZN0 1/20 0.41
▸ ALOX15 P16050 1/20 0.41
▸ CYP3A4 P08684 4/20 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 SCHEMBL25383162 1.00 LAP3 (0.52) LAP3ANPEPRNPEPDNPEPPKM
Hydrochloric Acid SCHEMBL25381350 0.82 SMN1; SMN2 (0.65) LAP3ANPEPRNPEPDNPEPKDM4E
Hydrochloric Acid SCHEMBL25381356 0.82 SMN1; SMN2 (0.65) LAP3ANPEPRNPEPDNPEPKDM4E
Hydrochloric Acid SCHEMBL30567907 0.81 PKM (0.43) LAP3ANPEPRNPEPDNPEPPKM
Hydrochloric Acid SCHEMBL31362073 0.81 PKM (0.43) LAP3ANPEPRNPEPDNPEPPKM
Hydrochloric Acid SCHEMBL17595507 0.81 LAP3 (0.66) LAP3ANPEPRNPEPDNPEPLTA4H
SCHEMBL17097365 0.79 LAP3 (0.68) LAP3ANPEPRNPEPDNPEPLTA4H
SCHEMBL7951029 0.79 LAP3 (0.68) LAP3ANPEPRNPEPDNPEPLTA4H
SCHEMBL16254379 0.79 PKM (0.50) PKMKDM4EHSPA1AHSPA5HSPA9
SCHEMBL25382013 0.77 SMN1; SMN2 (0.49) PKMKDM4EHSPA1AHSPA5HSPA9

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250064789-A1 KETOAMIDE DERIVATIVES AND PHARMACEUTICAL USES THEREOF WESTVAC BIOPHARMA CO., LTD. (CN) 2025-02-27 — — US disclosed
EP-4488264-A1 KETO AMIDE DERIVATIVES AND PHARMACEUTICAL USE THEREOF WestVac Biopharma Co., Ltd. (CN) 2025-01-08 — — EP disclosed
CN-116693447-B Ketone amide derivative and pharmaceutical application thereof 成都威斯克生物医药有限公司 2024-08-13 — — CN disclosed
WO-2023165334-A1 KETO AMIDE DERIVATIVES AND PHARMACEUTICAL USE THEREOF 成都威斯克生物医药有限公司 2023-09-07 — — WO disclosed
CN-116693447-A Ketone amide derivative and pharmaceutical application thereof 成都威斯克生物医药有限公司 2023-09-05 — — CN 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-20250064789-A1 KETOAMIDE DERIVATIVES AND PHARMACEUTICAL USES THEREOF ACE2, ACE, PKD2 LAP3 2675/4885ANPEP 939/4885RNPEP 547/4885

“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.

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