Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2825475

Cl.Cl.O=P(O)(O)C12CC3CC(CC(C3)C1)C2

nearest known ligand 0.95

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
GAA known ✓ P10253 1/20 0.95
GRIN2D known ✓ O15399 1/20 0.33
GRIN3B known ✓ O60391 1/20 0.33
GRIN1 known ✓ Q05586 1/20 0.33
GRIN2A known ✓ Q12879 1/20 0.33
GRIN2B known ✓ Q13224 1/20 0.33
GRIN2C known ✓ Q14957 1/20 0.33
GRIN3A known ✓ Q8TCU5 1/20 0.33
SIGMAR1 known ✓ Q99720 1/20 0.33
HSD11B1 known ✓ P28845 1/20 0.31
NPSR1 Q6W5P4 1/20 0.38
LMNA P02545 2/20 0.38
THRB P10828 2/20 0.38
POLB P06746 1/20 0.38
BLM P54132 1/20 0.38
PMP22 Q01453 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
EPHX2 P34913 2/20 0.36
EPHX1 P07099 2/20 0.36
TSHR P16473 3/20 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
SCHEMBL5736635 0.97 GAA (1.00) GAANPSR1LMNATHRBPOLB
Hydrochloric Acid SCHEMBL29127785 0.84 GAA (0.68) GAANPSR1LMNATHRBPOLB
SCHEMBL6466244 0.77 GAA (0.65) GAANPSR1LMNATHRBPOLB
SCHEMBL18207941 0.72 GAA (0.58) GAATSHR
SCHEMBL2825473 0.70 GAA (0.56) GAANPSR1LMNATHRBPOLB
Phosphoric Acid SCHEMBL27509750 0.70 GAA (0.56) GAANPSR1LMNATHRBPOLB
SCHEMBL1092162 0.70 GAA (0.56) GAANPSR1LMNATHRBPOLB
SCHEMBL1091418 0.70 GAA (0.56) GAANPSR1LMNATHRBPOLB
Phosphoric Acid SCHEMBL21408297 0.70 GAA (0.56) GAANPSR1LMNATHRBPOLB
Hydrochloric Acid SCHEMBL28398363 0.67 GAA (0.46) GAANPSR1LMNATHRBPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2243549-B1 A CATALYST SYSTEM LUCITE INT UK LTD (GB) 2020-09-02 EP disclosed
US-9802185-B2 Catalyst system LUCITE INTERNATIONAL UK LIMITED (GB) 2017-10-31 US disclosed
US-20150321186-A1 CATALYST SYSTEM Mitsubishi Chemical UK Limited (GB) 2015-11-12 US disclosed
EP-2243548-B1 A CATALYST SYSTEM LUCITE INT UK LTD (GB) 2015-11-11 EP disclosed
US-9040445-B2 Catalyst system LUCITE INTERNATIONAL UK LIMITED (GB) 2015-05-26 US disclosed
EP-1713582-B1 A CATALYST SYSTEM LUCITE INT UK LTD (GB) 2013-11-06 EP disclosed
EP-1554039-B1 A CATALYST SYSTEM COMPRISING A 1,2-BIS-(PHOSPHINO)METALLOCENE LIGAND LUCITE INT UK LTD (GB) 2013-07-03 EP disclosed
EP-2243549-A1 A catalyst system Lucite International UK Limited (GB) 2010-10-27 EP disclosed
EP-2243548-A1 A catalyst system Lucite International UK Limited (GB) 2010-10-27 EP disclosed
EP-1534427-B1 AN ADAMANTYL CATALYST SYSTEM LUCITE INT UK LTD (GB) 2009-10-21 EP disclosed
US-7371705-B2 Phospha-adamantane(s) catalytic system LUCITE INTERNATIONAL UK LIMITED (GB) 2008-05-13 US disclosed
US-20070282124-A1 Catalyst System LUCENT INTERNATIONAL UK LIMITED (GB) 2007-12-06 US disclosed
US-20060252935-A1 Catalyst system LUCITE INTERNATIONAL UK LIMITED (GB) 2006-11-09 US disclosed
EP-1713582-A1 A CATALYST SYSTEM Lucite International UK Limited (GB) 2006-10-25 EP disclosed
US-20060106259-A1 Phospha-adamantane(s) catalytic system LUCITE INTERNATIONAL UK LIMITED (GB) 2006-05-18 US disclosed
WO-2005079981-A1 A CATALYST SYSTEM LUCITE INTERNATIONAL UK LIMITED (GB) 2005-09-01 WO disclosed
EP-1554039-A2 A CATALYST SYSTEM COMPRISING A 1,2-BIS-(PHOSPHINOALKYL)FERROCENE LIGAND Lucite International UK Limited (GB) 2005-07-20 EP disclosed
EP-1534427-A1 AN ADAMANTYL CATALYTIC SYSTEM Lucite International UK Limited (GB) 2005-06-01 EP disclosed
WO-2004024322-A2 A CATALYST SYSTEM COMPRISING A 1,2-BIS-(PHOSPHINOALKYL) FERROCENE LIGAND LUCITE INTERNATIONAL UK LIMITED (GB) 2004-03-25 WO disclosed
WO-2004014552-A1 A PHOSPHA-ADAMANTANE (S) CATALYTIC SYSTEM LUCITE INTERNATIONAL UK LIMITED (GB) 2004-02-19 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-20060106259-A1 Phospha-adamantane(s) catalytic system ADORA2A, ADORA3, ADGRE5 GAA 3243/4885GRIN2D 567/4885GRIN3B 522/4885
US-20060252935-A1 Catalyst system ELOB, SOD1, ESR1 GAA 1618/4885GRIN2D 1910/4885GRIN3B 729/4885
US-20150321186-A1 CATALYST SYSTEM SMS, COASY, ABCB7 GAA 3561/4885GRIN2D 3265/4885GRIN3B 1989/4885
US-20070282124-A1 Catalyst System SMS, COASY, ABCB7 GAA 3561/4885GRIN2D 3265/4885GRIN3B 1989/4885

“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.