Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1998660

CCN(CC)Cc1cc(N)ccc1O.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
ACHE known ✓ P22303 3/20 1.00
PRKCI known ✓ P41743 1/20 0.96
CACNA1B known ✓ Q00975 1/20 0.64
JAK2 known ✓ O60674 1/20 0.59
CA2 known ✓ P00918 5/20 0.48
BCHE known ✓ P06276 1/20 0.43
GAA known ✓ P10253 1/20 0.40
KCNH2 known ✓ Q12809 1/20 0.40
POLB P06746 2/20 0.64
KDM4E B2RXH2 1/20 0.64
MEN1 O00255 1/20 0.64
ALDH1A1 P00352 1/20 0.64
MAPT P10636 1/20 0.64
THRB P10828 1/20 0.64
APEX1 P27695 1/20 0.64
MAPK1 P28482 1/20 0.64
HTT P42858 1/20 0.64
RECQL P46063 1/20 0.64
APBA1 Q02410 1/20 0.64
KMT2A Q03164 1/20 0.64

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 SCHEMBL1998656 1.00 ACHE (1.00) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL111109 0.98 PRKCI (1.00) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL29565648 0.98 PRKCI (1.00) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL5270782 0.91 PRKCI (0.86) ACHEPRKCIPOLBKDM4EMEN1
Hydrochloric Acid SCHEMBL29355056 0.85 ACHE (0.74) ACHEPRKCIPOLBKDM4EMEN1
Hydrochloric Acid SCHEMBL3336998 0.85 ACHE (0.74) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL7566226 0.84 PRKCI (0.73) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL5190111 0.84 PRKCI (0.74) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL1498028 0.83 PRKCI (0.73) ACHEPRKCIPOLBKDM4EMEN1
SCHEMBL28837441 0.83 PRKCI (0.73) ACHEPRKCIPOLBKDM4EMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120202243-A Thermosetting resin composition, cured film, substrate, and electronic component 捷恩智株式会社 2025-06-24 CN disclosed
EP-1885486-B1 AFFINITY ADSORBENTS FOR FACTOR VIII AND VON WILLEBRAND'S FACTOR PROMETIC BIOSCIENCES LTD (GB) 2016-03-23 EP disclosed
US-7960182-B2 Affinity adsorbents for Factor VIII and von Willebrand's Factor PROMETIC BIOSCIENCES LTD. (GB) 2011-06-14 US disclosed
US-20090275141-A1 Affinity Adsorbents for Factor VIII and Von Willebrand's Factor DEPARTMENT OF ECONOMIC DEVELOPMENT (IM) 2009-11-05 US disclosed
EP-1885486-A1 AFFINITY ADSORBENTS FOR FACTOR VIII AND VON WILLEBRAND'S FACTOR Prometic Biosciences Ltd (GB) 2008-02-13 EP disclosed
US-7214700-B2 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN INC. (US) 2007-05-08 US disclosed
WO-2006120427-A1 AFFINITY ADSORBENTS FOR FACTOR VIII AND VON WILLEBRAND'S FACTOR PROMETIC BIOSCIENCES LTD. (GB) 2006-11-16 WO disclosed
US-20040039196-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2004-02-26 US disclosed
US-20030216462-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2003-11-20 US disclosed
EP-1299355-A2 (2-OXINDOL-3-YLIDENYL)ACETIC ACID DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS Sugen, Inc. (US) 2003-04-09 EP disclosed
US-20020028828-A1 (2-oxindol-3-ylidenyl)acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2002-03-07 US disclosed
WO-2001083450-A2 (2-OXINDOL-3-YLIDENYL)ACETIC ACID DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS SUGEN, INC. (US) 2001-11-08 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 (4 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-20020028828-A1 (2-oxindol-3-ylidenyl)acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 ACHE 3714/4885PRKCI 23/4885CACNA1B 3573/4885
US-20040039196-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 ACHE 3714/4885PRKCI 23/4885CACNA1B 3573/4885
US-20030216462-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 ACHE 3714/4885PRKCI 23/4885CACNA1B 3573/4885
US-20090275141-A1 Affinity Adsorbents for Factor VIII and Von Willebrand's Factor F8, F13B, F12 ACHE 4873/4885PRKCI 2062/4885CACNA1B 1868/4885

“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.