Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4093025

CC1=C(C)C(C)(C)C([Zr]C2=C(C)C(C)=C(C)C2(C)C)=C1C.Cl

nearest known ligand 0.32

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 1)

geneUniProtsupporting neighboursconfidence
CTSD P07339 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
Hydrochloric Acid SCHEMBL137722 1.00 CTSD (0.32) CTSD
Hydrochloric Acid SCHEMBL8162359 1.00 CTSD (0.32) CTSD
SCHEMBL248760 0.97 CTSD (0.33) CTSD
Chloromethane SCHEMBL9353096 0.95 CTSD (0.30) CTSD
Fluoride SCHEMBL5613215 0.94 CTSD (0.32) CTSD
Bromide SCHEMBL7870148 0.94 CTSD (0.32) CTSD
SCHEMBL3845460 0.94 CTSD (0.32) CTSD
Methane SCHEMBL4577018 0.94 CTSD (0.32) CTSD
SCHEMBL8652405 0.92 CTSD (0.31) CTSD
Chloromethane SCHEMBL3682470 0.92 CTSD (0.31) CTSD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7074736-B2 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY (US) 2006-07-11 US claimed
EP-1201684-A2 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY (US) 2002-05-02 EP claimed
US-20020052536-A1 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY 2002-05-02 US claimed
EP-3187500-B1 METHOD FOR PRODUCING ANTITUMOR AGENT USING A HOMOGENIZER EISAI R&D MAN CO LTD (JP) 2019-01-02 EP disclosed
EP-3187500-A1 METHOD FOR PRODUCING ANTITUMOR AGENT USING HOMOGENIZER Eisai R&D Management Co., Ltd. (JP) 2017-07-05 EP disclosed
US-20090203771-A1 NOVEL INTERMEDIATE FOR HALICHONDRIN B ANALOG SYNTHESIS AND NOVEL DESULFONYLATION REACTION USED FOR THE INTERMEDIATE EISAI R&D MANAGEMENT CO., LTD. (JP) 2009-08-13 US disclosed
US-7074736-B2 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY (US) 2006-07-11 US disclosed
EP-1160008-B1 Gas distributor plate for a gas phase polymerization apparatus MITSUI CHEMICALS INC (JP) 2003-07-23 EP disclosed
EP-1201684-A2 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY (US) 2002-05-02 EP disclosed
US-20020052536-A1 Hydrozirconated matrix and process for polyolefin production ROHM AND HAAS COMPANY 2002-05-02 US disclosed
EP-0721798-B1 Gas distributor plate for a gas phase polymerisation apparatus MITSUI CHEMICALS INC (JP) 2002-03-06 EP disclosed
EP-1160008-A1 Gas distributor plate for a gas phase polymerization apparatus Mitsui Chemicals, Inc. (JP) 2001-12-05 EP disclosed
US-5753191-A UNIFORMLY DIFFUSES GAS FLOW IN FLUIDIZED BED ZONE MITSUI CHEMICALS, INC. (JP) 1998-05-19 US disclosed
EP-0721798-A2 Gas distributor plate for a gas phase polymerisation apparatus MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1996-07-17 EP disclosed
EP-0576213-A2 Process for polymerizing olefins MITSUBISHI CHEMICAL CORPORATION (JP) 1993-12-29 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 (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-20020052536-A1 Hydrozirconated matrix and process for polyolefin production HOGA1, PPIP5K2, HPD CTSD 877/4885
US-20090203771-A1 NOVEL INTERMEDIATE FOR HALICHONDRIN B ANALOG SYNTHESIS AND NOVEL DESULFONYLATION REACTION USED FOR THE INTERMEDIATE NISCH, BMP2, SHH CTSD 3524/4885

“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.