Hydrochloric Acid

Hydrochloric Acid

SCHEMBL852064

C(c1ccccc1)=[Ru](=C1N(C2CCCCC2)CCN1C1CCCCC1)=C1N(C2CCCCC2)CCN1C1CCCCC1.Cl.Cl

nearest known ligand 0.40

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 15)

geneUniProtsupporting neighboursconfidence
HSD11B1 known ✓ P28845 1/20 0.38
GAA known ✓ P10253 3/20 0.35
HSP90AA1 known ✓ P07900 2/20 0.34
OPRM1 known ✓ P35372 1/20 0.32
OPRD1 known ✓ P41143 1/20 0.32
OPRK1 known ✓ P41145 1/20 0.32
SLC18A3 Q16572 1/20 0.38
ALDH1A1 P00352 4/20 0.35
KDM4E B2RXH2 3/20 0.35
LMNA P02545 3/20 0.35
HPGD P15428 2/20 0.35
SMN1; SMN2 Q16637 3/20 0.34
MAPK1 P28482 1/20 0.34
POLB P06746 2/20 0.33
OGFRL1 Q5TC84 1/20 0.32

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
SCHEMBL4607065 0.98 HSD11B1 (0.39) HSD11B1SLC18A3ALDH1A1KDM4EGAA
Hydrochloric Acid SCHEMBL1008609 0.75 SLC18A3 (0.35) SLC18A3ALDH1A1KDM4EGAASMN1; SMN2
SCHEMBL4607064 0.73 SLC18A3 (0.36) SLC18A3ALDH1A1KDM4EGAASMN1; SMN2
SCHEMBL28898023 0.72 HSD11B1 (0.34) HSD11B1SLC18A3ALDH1A1KDM4EGAA
Hydrochloric Acid SCHEMBL1006742 0.70 HSD11B1 (0.39) HSD11B1SLC18A3ALDH1A1KDM4EGAA
SCHEMBL819176 0.68 HSD11B1 (0.38) HSD11B1SLC18A3ALDH1A1KDM4EGAA
Hydrochloric Acid SCHEMBL6879846 0.66 CYP2D6 (0.32) ALDH1A1HPGD
Hydrochloric Acid SCHEMBL1007232 0.64 HSD11B1 (0.35) HSD11B1SLC18A3ALDH1A1KDM4EGAA
Hydrochloric Acid SCHEMBL28132082 0.63 OPRM1 (0.42) HSD11B1SLC18A3GAAPOLBOPRM1
Hydrochloric Acid SCHEMBL1045367 0.63 OPRM1 (0.42) HSD11B1SLC18A3GAAPOLBOPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250215137-A1 COPOLYMER, RUBBER COMPOSITION AND CROSSLINKED RUBBER ZEON CORPORATION (JP) 2025-07-03 US disclosed
US-20250215136-A1 RUBBER COMPOSITION AND CROSSLINKED RUBBER PRODUCT ZEON CORPORATION (JP) 2025-07-03 US disclosed
US-20250091969-A1 CYCLOPENTENE RECOVERY METHOD ZEON CORPORATION (JP) 2025-03-20 US disclosed
EP-4502059-A1 RUBBER COMPOSITION AND CROSSLINKED RUBBER PRODUCT Zeon Corporation (JP) 2025-02-05 EP disclosed
EP-4502014-A1 COPOLYMER, RUBBER COMPOSITION AND CROSSLINKED RUBBER Zeon Corporation (JP) 2025-02-05 EP disclosed
WO-2025013873-A1 CYCLOPENTENE RECOVERY METHOD 日本ゼオン株式会社 2025-01-16 WO disclosed
EP-4461720-A1 CYCLOPENTENE RECOVERY METHOD Zeon Corporation (JP) 2024-11-13 EP disclosed
US-11707648-B2 Golf ball SUMITOMO RUBBER INDUSTRIES, LTD. (JP) 2023-07-25 US disclosed
WO-2023132366-A1 CYCLOPENTENE RECOVERY METHOD 日本ゼオン株式会社 2023-07-13 WO disclosed
US-11390709-B2 Liquid copolymer formed by ring-opening copolymerization of cyclopentene, crosslinkable composition, and crosslinked rubber object ZEON CORPORATION (JP) 2022-07-19 US disclosed
US-7037993-B2 Norbornene-based ring-opening polymerization polymer, product of hydrogenation of norbornene-based ring-opening polymerization polymer, and processes for producing these ZEON CORPORATION (JP) 2006-05-02 US disclosed
EP-1640153-A1 MULTILAYER BODY AND METHOD FOR PRODUCING SAME Zeon Corporation (JP) 2006-03-29 EP disclosed
EP-1589055-A1 PROCESS FOR PRODUCING CYCLOOLEFIN RESIN FILM AND PROCESS FOR PRODUCING CYCLOOLEFIN POLYMER SHEET OR FILM Zeon Corporation (JP) 2005-10-26 EP disclosed
EP-1589054-A1 POLYMERIZABLE COMPOSITION, THERMOPLASTIC RESIN COMPOSITION, CROSSLINKED RESIN, AND CROSSLINKED RESIN COMPOSITE MATERIALS Zeon Corporation (JP) 2005-10-26 EP disclosed
US-20050148746-A1 Norbornene-based ring-opening polymerization polymer, product of hydrogenation of norbornene-based ring-opening polymerization polymer, and processes for producing these ZEON CORPORATION (JP) 2005-07-07 US disclosed
US-6908970-B2 Process for producing hydrogenated product of cyclic olefin polymer prepared through ring-opening polymerization ZEON CORPORATION (JP) 2005-06-21 US disclosed
EP-1535941-A1 PROCESSES FOR PRODUCING THERMOPLASTIC RESINS, CROSSLINKED RESINS AND CROSSLINKED RESIN COMPOSITE MATERIALS ZEON CORPORATION (JP) 2005-06-01 EP disclosed
US-20030050406-A1 Process for producing hydrogenated product of cyclic olefin polymer prepared through ring-opening polymerization ZEON CORPORATION 2003-03-13 US disclosed
US-6486264-B1 Process for producing hydrogenated ring-opening polymerization polymer of cycloolefin ZEON CORPORATION (JP) 2002-11-26 US disclosed
EP-1197509-A1 PROCESS FOR PRODUCING HYDROGENATED RING-OPENING POLYMERIZATION POLYMER OF CYCLOOLEFIN Nippon Zeon Co., Ltd. (JP) 2002-04-17 EP 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 (1 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-20250091969-A1 CYCLOPENTENE RECOVERY METHOD CYC1, CYCS, DHPS HSD11B1 310/4885GAA 4437/4885HSP90AA1 2402/4885

“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.