Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3950971

Cl.N[C@@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1

nearest known ligand 0.75

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
▸ TACR1 known ✓ P25103 7/20 0.75
▸ HSP90AA1 known ✓ P07900 1/20 0.58
▸ HSP90AB1 known ✓ P08238 1/20 0.58
▸ GAA known ✓ P10253 1/20 0.53
▸ MAPT P10636 3/20 0.67
▸ MEN1 O00255 2/20 0.67
▸ KMT2A Q03164 2/20 0.67
▸ KDM4E B2RXH2 2/20 0.67
▸ LMNA P02545 1/20 0.67
▸ MPO P05164 1/20 0.67
▸ TSHR P16473 1/20 0.67
▸ BLM P54132 1/20 0.67
▸ PMP22 Q01453 1/20 0.67
▸ HIF1A Q16665 1/20 0.67
▸ LTA4H P09960 1/20 0.58
▸ PLA2G2A P14555 1/20 0.58
▸ LNPEP Q9UIQ6 1/20 0.58
▸ NMBR P28336 2/20 0.55
▸ ERAP1 Q9NZ08 3/20 0.55
▸ SMN1; SMN2 Q16637 1/20 0.54

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 SCHEMBL28897384 1.00 TACR1 (0.75) TACR1MAPTMEN1KMT2AKDM4E
Hydrochloric Acid SCHEMBL29401056 1.00 TACR1 (0.75) TACR1MAPTMEN1KMT2AKDM4E
Hydrochloric Acid SCHEMBL29401116 1.00 TACR1 (0.75) TACR1MAPTMEN1KMT2AKDM4E
Hydrochloric Acid SCHEMBL4685036 1.00 TACR1 (0.75) TACR1MAPTMEN1KMT2AKDM4E
SCHEMBL1167913 0.99 TACR1 (0.77) TACR1MAPTMEN1KMT2AKDM4E
SCHEMBL8025702 0.99 TACR1 (0.77) TACR1MAPTMEN1KMT2AKDM4E
SCHEMBL1167914 0.99 TACR1 (0.77) TACR1MAPTMEN1KMT2AKDM4E
SCHEMBL31119836 0.99 TACR1 (0.77) TACR1MAPTMEN1KMT2AKDM4E
Phosphoric Acid SCHEMBL27857626 0.94 TACR1 (0.71) TACR1MAPTMEN1KMT2AKDM4E
Trifluoroacetic Acid SCHEMBL8787543 0.92 TACR1 (0.68) TACR1MAPTMEN1KMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111574710-B Dendritic tryptophan compound, preparation method thereof and application thereof as antibacterial agent 威海晨源分子新材料有限公司 2022-07-01 — — CN claimed
CN-111518275-B Dendritic tryptophan compound, preparation method thereof and application thereof as virus invasion inhibitor 威海晨源分子新材料有限公司 2022-07-01 — — CN claimed
CN-111574710-A Dendritic tryptophan compound, preparation method thereof and application thereof as antibacterial agent 威海晨源分子新材料有限公司 2020-08-25 — — CN claimed
CN-111518275-A Dendritic tryptophan compound, preparation method thereof and application thereof as virus invasion inhibitor 威海晨源分子新材料有限公司 2020-08-11 — — CN claimed
JP-11228573-A — — None — — JP disclosed
JP-4327592-A — — None — — JP disclosed
CN-115477656-B Dioxahexacyclic-tetrahydrocarboline-3-formylamino acid targeting P-selectin, preparation and application 首都医科大学 2024-04-19 — — CN disclosed
CN-114644583-B Indole derivative and preparation method and application thereof 中国医学科学院医药生物技术研究所 2024-02-06 — — CN disclosed
CN-115477656-A Dioxane-tetrahydro carboline-3-formylamino acid with P-selectin as target and preparation and application thereof 首都医科大学 2022-12-16 — — CN disclosed
CN-111574710-B Dendritic tryptophan compound, preparation method thereof and application thereof as antibacterial agent 威海晨源分子新材料有限公司 2022-07-01 — — CN disclosed
CN-111518275-B Dendritic tryptophan compound, preparation method thereof and application thereof as virus invasion inhibitor 威海晨源分子新材料有限公司 2022-07-01 — — CN disclosed
CN-114644583-A Indole derivative and preparation method and application thereof 中国医学科学院医药生物技术研究所 2022-06-21 — — CN disclosed
JP-H04327592-A PHOSPHONIC ACID AMIDE DERIVATIVE NIPPON CHEMIPHAR CO LTD 1992-11-17 — — JP disclosed
WO-1992013545-A1 ENDOTHELIN CONVERTING ENZYME INHIBITORS ABBOTT LABORATORIES (US) 1992-08-20 — — WO disclosed
WO-1991012267-A1 ANTI-OXIDATIVE AND ANTI-INFLAMMATORY METAL:PEPTIDE COMPLEXES AND USES THEREOF PROCYTE CORPORATION (US) 1991-08-22 — — WO disclosed
US-4978669-A ALTERING MACRONUTRIENT PREFERENCE NEUREX CORPORATION (US) 1990-12-18 — — US disclosed
WO-1990014827-A1 METHOD OF SUPPRESSING APPETITE BY ADMINISTRATION OF TETRAHYDRO-β-CARBOLINE DERIVATIVES NEUREX CORPORATION (US) 1990-12-13 — — WO disclosed
EP-0190588-A1 Quinazolino-1,4-benzodiazepin-6,9-diones, processes for their preparation and pharmaceutical compositions containing them MERCK & CO. INC. (US) 1986-08-13 — — EP disclosed
US-4554272-A CHOLECYSTOKININ INHIBITORS MERCK & CO., INC. (US) 1985-11-19 — — US disclosed
US-3953416-A Synthetic decapeptide having the activity of the luteinizing hormone releasing hormone and method for manufacturing the same FOLKERS KARL 1976-04-27 — — US disclosed
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