Hydrochloric Acid

Hydrochloric Acid

SCHEMBL607840

CC(N)c1cccc2ccccc12.Cl

nearest known ligand 0.54

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
GLA known ✓ P06280 1/20 0.48
ADRA2A known ✓ P08913 4/20 0.47
ADRA2B known ✓ P18089 4/20 0.47
ADRA2C known ✓ P18825 4/20 0.47
SLC6A2 known ✓ P23975 1/20 0.46
SLC6A4 known ✓ P31645 1/20 0.46
SLC6A3 known ✓ Q01959 1/20 0.46
ADRA1A known ✓ P35348 2/20 0.45
ADRA1D known ✓ P25100 1/20 0.45
ADRA1B known ✓ P35368 1/20 0.45
ALDH1A1 P00352 4/20 0.54
CYP1A2 P05177 2/20 0.54
CYP2C9 P11712 1/20 0.54
CYP2C19 P33261 1/20 0.54
LMNA P02545 1/20 0.48
CYP3A4 P08684 2/20 0.45
CYP2D6 P10635 1/20 0.45
NFKB1 P19838 1/20 0.45
PNMT P11086 1/20 0.45
AOC3 Q16853 1/20 0.45

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 SCHEMBL28349939 1.00 ALDH1A1 (0.54) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
Hydrochloric Acid SCHEMBL31221886 1.00 ALDH1A1 (0.54) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
Hydrochloric Acid SCHEMBL7597590 1.00 ALDH1A1 (0.54) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
Hydrochloric Acid SCHEMBL30933601 1.00 ALDH1A1 (0.54) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
Hydrochloric Acid SCHEMBL6251235 1.00 ALDH1A1 (0.54) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
SCHEMBL128713 0.98 ALDH1A1 (0.56) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
SCHEMBL335062 0.98 ALDH1A1 (0.56) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
SCHEMBL21538667 0.98 ALDH1A1 (0.56) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
SCHEMBL353568 0.98 ALDH1A1 (0.56) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA
SCHEMBL29367357 0.98 ALDH1A1 (0.56) ALDH1A1CYP1A2CYP2C9CYP2C19LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2012127385-A1 BENZO [B] [1, 4] OXAZIN DERIVATIVES AS CALCIUM SENSING RECEPTOR MODULATORS LUPIN LIMITED (IN) 2012-09-27 WO claimed
US-20070185346-A1 Kit for automated resolving agent selection and method thereof VAIDYA NITEEN A 2007-08-09 US claimed
EP-1148876-A4 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORP (US) 2003-07-23 EP claimed
EP-1148876-A1 CALCILYTIC COMPOUNDS SmithKline Beecham Corporation (US) 2001-10-31 EP claimed
WO-2000045816-A1 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (GB) 2000-08-10 WO claimed
CN-119662740-A Stable, efficient and environment-friendly silver nanoparticle lactobacillus biosynthesis method and application 郑州轻工业大学 2025-03-21 CN disclosed
US-20240350643-A1 PROTEIN DEGRADATION AGENT SUZHOU KINTOR PHARMACEUTICALS, INC. (CN) 2024-10-24 US disclosed
CN-118724676-A Entecavir Process for the preparation of intermediates 南京工业大学 2024-10-01 CN disclosed
CN-118164913-A Indenopiperidine derivatives, and preparation method and application thereof 浙江大学 2024-06-11 CN disclosed
EP-4361141-A1 PROTEIN DEGRADATION AGENT Suzhou Kintor Pharmaceuticals, Inc. (CN) 2024-05-01 EP disclosed
CN-117545749-A Protein degradation agent 苏州开拓药业股份有限公司 2024-02-09 CN disclosed
CN-115504963-A C-Myc protein degradation agent 苏州开拓药业股份有限公司 2022-12-23 CN disclosed
WO-2007092264-A2 KIT FOR AUTOMATED RESOLVING AGENT SELECTION AND METHOD THEREOF VAIDYA NITEEN A (US) 2007-08-16 WO disclosed
US-20070185346-A1 Kit for automated resolving agent selection and method thereof VAIDYA NITEEN A 2007-08-09 US disclosed
US-20060004230-A1 Process for the preparation of terbinafine and salts thereof CHEMAGIS LTD. (IL) 2006-01-05 US disclosed
EP-1148876-A4 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORP (US) 2003-07-23 EP disclosed
EP-1148876-A1 CALCILYTIC COMPOUNDS SmithKline Beecham Corporation (US) 2001-10-31 EP disclosed
WO-2000045816-A1 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (GB) 2000-08-10 WO disclosed
EP-0907631-A1 INORGANIC ION RECEPTOR-ACTIVE COMPOUNDS NPS PHARMACEUTICALS, INC. (US) 1999-04-14 EP disclosed
WO-1997041090-A1 INORGANIC ION RECEPTOR-ACTIVE COMPOUNDS NPS PHARMACEUTICALS, INC. (US) 1997-11-06 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-20240350643-A1 PROTEIN DEGRADATION AGENT MYC, MYCBP, MYCBP2 GLA 1300/4885ADRA2A 4557/4885ADRA2B 4680/4885
US-20060004230-A1 Process for the preparation of terbinafine and salts thereof TPMT, HNMT, DHPS GLA 3718/4885ADRA2A 3672/4885ADRA2B 2349/4885

“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.