Hydrochloric Acid

Hydrochloric Acid

SCHEMBL846153

Cl.Cl.ClCCCN1CCN(CCCl)CC1

nearest known ligand 0.46

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 18)

geneUniProtsupporting neighboursconfidence
HRH3 known ✓ Q9Y5N1 1/20 0.38
SIGMAR1 known ✓ Q99720 1/20 0.33
GNAI3 P08754 1/20 0.37
GNAO1 P09471 1/20 0.37
GNAI1 P63096 1/20 0.37
RAD52 P43351 1/20 0.36
ALOX15 P16050 1/20 0.35
KDM4E B2RXH2 1/20 0.33
MEN1 O00255 1/20 0.33
USP2 O75604 1/20 0.33
LMNA P02545 1/20 0.33
MAPT P10636 1/20 0.33
HPGD P15428 1/20 0.33
ALOX12 P18054 1/20 0.33
KMT2A Q03164 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
TDP1 Q9NUW8 1/20 0.33

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 SCHEMBL28996755 1.00 HRH3 (0.38) HRH3GNAI3GNAO1GNAI1RAD52
SCHEMBL10552270 0.97 HRH3 (0.39) HRH3GNAI3GNAO1GNAI1RAD52
SCHEMBL23853043 0.91 HRH3 (0.43) HRH3GNAI3GNAO1GNAI1ALOX15
SCHEMBL3412350 0.91
Hydrochloric Acid SCHEMBL29891395 0.88 ALOX15 (0.42) GNAI3GNAO1GNAI1RAD52ALOX15
SCHEMBL7511785 0.85 ALOX15 (0.44) HRH3RAD52ALOX15KDM4ESIGMAR1
SCHEMBL11570567 0.85
Hydrochloric Acid SCHEMBL409216 0.84 PAOX (0.45) HRH3GNAI3GNAO1GNAI1MEN1
Hydrochloric Acid SCHEMBL374447 0.84 PAOX (0.45) HRH3GNAI3GNAO1GNAI1MEN1
Hydrochloric Acid SCHEMBL737731 0.83 HRH3 (0.57) HRH3RAD52LMNAMAPTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12624118-B2 Trispecific binding molecules against BCMA and uses thereof NOVARTIS AG (CH) 2026-05-12 US disclosed
WO-2026085795-A1 SILENCED FC REGIONS PROTEINTECH GROUP, INC. (US) 2026-04-30 WO disclosed
US-20260035473-A1 BINDING MOLECULES AGAINST BCMA AND USES THEREOFPrivate view NOVARTIS AG (CH) 2026-02-05 US disclosed
US-20250326855-A1 ANTI-GLYCO-CD44 ANTIBODIES AND THEIR USES GO THERAPEUTICS, INC. (US) 2025-10-23 US disclosed
EP-4630456-A1 ANTI-CMET ANTIBODY DRUG CONJUGATES AND THERAPEUTIC USES THEREOF Mythic Therapeutics, Inc. (US) 2025-10-15 EP disclosed
US-20250304716-A1 ANTI-GLYCO-MUC1 ANTIBODIES AND THEIR USES GO THERAPEUTICS, INC. (US) 2025-10-02 US disclosed
US-20250223359-A1 CD19 BINDING MOLECULES AND USES THEREOF NOVARTIS AG (CH) 2025-07-10 US disclosed
US-20250136701-A1 ANTI-GLYCO-CMET ANTIBODIES AND THEIR USES GO THERAPEUTICS, INC. (US) 2025-05-01 US disclosed
US-12275795-B2 Binding molecules against BCMA and uses thereof NOVARTIS AG (CH) 2025-04-15 US disclosed
US-12269892-B2 Anti-glyco-MUC1 antibodies and their uses GO THERAPEUTICS, INC. (US) 2025-04-08 US disclosed
US-20050090529-A1 3,5 Disubstituted indazole compounds with nitrogen-bearing 5-membered heterocycles, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation PFIZER INC 2005-04-28 US disclosed
US-20050090509-A1 Thienopyridine-phenylacetamides and their derivatives useful as new anti-angiogenic agents Agouron Pharmaceuticals,Inc. 2005-04-28 US disclosed
US-20050070508-A1 Napthalene carboxamides and their derivatives useful as new anti-angiogenic agents AGOURON PHARMACEUTICALS, INC. 2005-03-31 US disclosed
WO-2005021554-A1 THIENOPYRIDINE-PHENYLACET AMIDES AND THEIR DERIVATIVES USEFUL AS NEW ANTI-ANGIOGENIC AGENTS PFIZER INC. (US) 2005-03-10 WO disclosed
WO-2005021553-A1 NAPHTHALENE CARBOXAMIDES AND THEIR DERIVATIVES USEFUL AS NEW ANTI-ANGIOGENIC AGENTS PFIZER INC. (US) 2005-03-10 WO disclosed
US-20050026960-A1 3, 5 disubstituted indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation AGOURON PHARMACEUTICALS, INC. 2005-02-03 US disclosed
WO-2005009997-A1 3,5 DISUBSTITUTED INDAZOLE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, AND METHODS FOR MEDIATING OR INHIBITING CELL PROLIFERATION PFIZER INC. (US) 2005-02-03 WO disclosed
US-20040224988-A1 Dosage forms and methods of treatment using VEGFR inhibitors AGOURON PHARMACEUTICALS, INC. 2004-11-11 US disclosed
WO-2004087152-A1 DOSAGE FORMS COMPRISING AG013736 PFIZER INC. (US) 2004-10-14 WO disclosed
US-20040192735-A1 Indazole compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use AGOURON PHARMACEUTICALS, INC. 2004-09-30 US 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 (14 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-20050090509-A1 Thienopyridine-phenylacetamides and their derivatives useful as new anti-angiogenic agents CCNA1, PGF, CCNA2 HRH3 203/4885SIGMAR1 1615/4885GNAI3 1988/4885
US-12269892-B2 Anti-glyco-MUC1 antibodies and their uses MUC1, SIGLEC7, SIGLEC9 HRH3 3686/4885SIGMAR1 4741/4885GNAI3 546/4885
US-20250136701-A1 ANTI-GLYCO-CMET ANTIBODIES AND THEIR USES CD2BP2, CSGALNACT1, DNTT HRH3 2463/4885SIGMAR1 3729/4885GNAI3 647/4885
US-20040192735-A1 Indazole compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use CDK3, BRAF, CNKSR1 HRH3 1831/4885SIGMAR1 4829/4885GNAI3 403/4885
US-20050026960-A1 3, 5 disubstituted indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation CDK3, CDK4, CDKL3 HRH3 2564/4885SIGMAR1 4876/4885GNAI3 405/4885
US-20250326855-A1 ANTI-GLYCO-CD44 ANTIBODIES AND THEIR USES CD44, SIGLEC7, SIGLEC9 HRH3 1205/4885SIGMAR1 2783/4885GNAI3 1731/4885
US-20260035473-A1 BINDING MOLECULES AGAINST BCMA AND USES THEREOFPrivate view BCL9, BRCA1, VCAM1 HRH3 120/4885SIGMAR1 423/4885GNAI3 4848/4885
US-12624118-B2 Trispecific binding molecules against BCMA and uses thereof CD2, CD40, CD22 HRH3 35/4885SIGMAR1 866/4885GNAI3 4294/4885
US-20050070508-A1 Napthalene carboxamides and their derivatives useful as new anti-angiogenic agents CCNA1, CCNA2, CCNT1 HRH3 126/4885SIGMAR1 498/4885GNAI3 2265/4885
US-20050090529-A1 3,5 Disubstituted indazole compounds with nitrogen-bearing 5-membered heterocycles, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation CDK3, CDK4, CDK9 HRH3 2212/4885SIGMAR1 4833/4885GNAI3 435/4885
US-20040224988-A1 Dosage forms and methods of treatment using VEGFR inhibitors FLT1, FLT4, KDR HRH3 3457/4885SIGMAR1 1838/4885GNAI3 1796/4885
US-20250223359-A1 CD19 BINDING MOLECULES AND USES THEREOF CD22, BCL9, CD2 HRH3 1905/4885SIGMAR1 4076/4885GNAI3 1457/4885
US-12275795-B2 Binding molecules against BCMA and uses thereof EPCAM, CD40, BCR HRH3 1928/4885SIGMAR1 2977/4885GNAI3 2255/4885
US-20250304716-A1 ANTI-GLYCO-MUC1 ANTIBODIES AND THEIR USES MUC1, SIGLEC7, SIGLEC9 HRH3 3686/4885SIGMAR1 4741/4885GNAI3 546/4885

“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.