Hydrochloric Acid

Hydrochloric Acid

SCHEMBL17261836

CC(C)c1ccc(Cn2ccc3c4c(N)nc(NC5CC5)nc4ccc32)cc1.Cl.Cl

nearest known ligand 0.98

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 16)

geneUniProtsupporting neighboursconfidence
▸ F2R P25116 15/20 0.98
▸ KDM4E B2RXH2 1/20 0.98
▸ MEN1 O00255 1/20 0.98
▸ TP53 P04637 1/20 0.98
▸ CYP1A2 P05177 1/20 0.98
▸ CYP3A4 P08684 1/20 0.98
▸ CYP2D6 P10635 1/20 0.98
▸ MAPT P10636 1/20 0.98
▸ HPGD P15428 1/20 0.98
▸ ALOX15 P16050 1/20 0.98
▸ TSHR P16473 1/20 0.98
▸ CYP2C19 P33261 1/20 0.98
▸ KMT2A Q03164 1/20 0.98
▸ HSD17B10 Q99714 1/20 0.98
▸ SLC2A1 P11166 3/20 0.49
▸ DHFR P00374 1/20 0.48

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 SCHEMBL29514998 1.00 F2R (0.98) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL29413913 0.99 F2R (1.00) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL1760395 0.99 F2R (1.00) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL35210414 0.99 F2R (1.00) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL15324357 0.87 F2R (0.78) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL24166774 0.86 F2R (0.77) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL24164678 0.84 F2R (0.74) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL24166733 0.84 F2R (0.73) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL4256302 0.84 F2R (0.73) F2RKDM4EMEN1TP53CYP1A2
SCHEMBL24165333 0.82 F2R (0.71) F2RKDM4EMEN1TP53CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12000825-B2 Method of selecting stem cells having ability to produce extracellular vesicles with high efficiency using activation of protease-activated receptor-mediated signaling pathways SAMSUNG LIFE PUBLIC WELFARE FOUNDATION (KR) 2024-06-04 — — US disclosed
EP-3143036-B1 PAR-1 BASED THERAPEUTIC CONJUGATES AND USES THEREOF TEL HASHOMER MEDICAL RES INFRASTRUCTURE & SERVICES LTD (IL) 2023-08-02 — — EP disclosed
EP-3964566-A1 METHOD FOR SELECTING STEM CELLS HAVING ABILITY TO PRODUCE EXTRACELLULAR VESICLES WITH HIGH EFFICIENCY BY USING ACTIVITY OF PROTEASE-ACTIVATED RECEPTOR-MEDIATED SIGNALING PATHWAYS Samsung Life Public Welfare Foundation (KR) 2022-03-09 — — EP disclosed
CN-113767166-A Method for selecting stem cells having the ability to efficiently produce extracellular vesicles using protease-activated receptor-mediated activation of signaling pathways 社会福祉法人三星生命公益财团 2021-12-07 — — CN disclosed
US-20210255169-A1 Method Of Selecting Stem Cells Having Ability To Produce Extracellular Vesicles With High Efficiency Using Activation Of Protease-Activated Receptor-Mediated Signaling Pathways SAMSUNG LIFE PUBLIC WELFARE FOUNDATION (KR) 2021-08-19 — — US disclosed
US-11077109-B2 Compounds having antibacterial activity and methods of use THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2021-08-03 — — US disclosed
US-20190201401-A1 COMPOUNDS HAVING ANTIBACTERIAL ACTIVITY AND METHODS OF USE THE TRUSTEES OF PRINCETON UNIVERSITY 2019-07-04 — — US disclosed
US-10028999-B2 PAR-1 based therapeutic conjugates and uses thereof TEL HASHOMER MEDICAL RESEARCH INFRASTRUCTURE AND SERVICES LTD. (IL) 2018-07-24 — — US disclosed
EP-3143036-A1 PAR-1 BASED THERAPEUTIC CONJUGATES AND USES THEREOF Tel Hashomer Medical Research Infrastructure and Services Ltd. (IL) 2017-03-22 — — EP disclosed
US-20170072014-A1 PAR-1 BASED THERAPEUTIC CONJUGATES AND USES THEREOF TEL HASHOMER MEDICAL RESEARCH INFRASTRUCTURE AND SERVICES LTD. (IL) 2017-03-16 — — US disclosed
WO-2015173802-A1 PAR-1 BASED THERAPEUTIC CONJUGATES AND USES THEREOF TEL HASHOMER MEDICAL RESEARCH INFRASTRUCTURE AND SERVICES LTD. (IL) 2015-11-19 — — WO 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-20190201401-A1 COMPOUNDS HAVING ANTIBACTERIAL ACTIVITY AND METHODS OF USE MMP8, MRPL21, CLPP F2R 1882/4885KDM4E 4633/4885MEN1 3504/4885
US-11077109-B2 Compounds having antibacterial activity and methods of use MMP8, MRPL21, CLPP F2R 1882/4885KDM4E 4633/4885MEN1 3504/4885

“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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