Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2302788

Cl.N=C(N)c1ccc(N)c([N+](=O)[O-])c1

nearest known ligand 0.65

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 17)

geneUniProtsupporting neighboursconfidence
PARP1 known ✓ P09874 1/20 0.46
LMNA P02545 1/20 0.65
PRSS1 P07477 9/20 0.60
PRSS2 P07478 1/20 0.58
PRSS3 P35030 1/20 0.58
TDP1 Q9NUW8 3/20 0.55
MAPT P10636 3/20 0.55
MEN1 O00255 2/20 0.55
KMT2A Q03164 2/20 0.55
POLB P06746 1/20 0.55
ALDH1A1 P00352 1/20 0.55
CYP3A4 P08684 1/20 0.55
ALOX15 P16050 1/20 0.55
TSHR P16473 1/20 0.51
PLG P00747 1/20 0.46
CRHBP P24387 1/20 0.45
CRHR2 Q13324 1/20 0.45

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
SCHEMBL7384522 0.98 LMNA (0.67) LMNAPRSS1PRSS2PRSS3TDP1
Hydrochloric Acid SCHEMBL6369255 0.84 LMNA (0.72) LMNATDP1MAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL13269367 0.83 PRSS1 (0.60) LMNAPRSS1PRSS2PRSS3MAPT
SCHEMBL12857754 0.83 LMNA (0.65) LMNATDP1MAPTMEN1KMT2A
SCHEMBL1470130 0.82 LMNA (0.74) LMNATDP1MAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL11294839 0.82 LMNA (0.59) LMNAPRSS1TDP1MAPTMEN1
Hydrochloric Acid SCHEMBL9202510 0.81 TSHR (0.63) PRSS1PRSS2PRSS3MAPTKMT2A
SCHEMBL4873598 0.81 PRSS1 (0.59) LMNAPRSS1PRSS2PRSS3MAPT
SCHEMBL1063063 0.81 LMNA (0.67) LMNATDP1MAPTMEN1KMT2A
SCHEMBL31174170 0.80 LMNA (0.77) LMNATDP1MAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109553608-A The purposes of a kind of five yuan of 6-membered heterocyclic compounds and preparation method thereof and treatment tumour 北京大学 2019-04-02 CN disclosed
CN-109554469-A The tumour cell and its molecular marker of T cell acute lymphatic leukemia 北京大学 2019-04-02 CN disclosed
CN-109554468-A PU.1 inhibitor and its application 北京大学 2019-04-02 CN disclosed
US-9181280-B2 Factor VIIa inhibitor PHARMACYCLICS LLC (US) 2015-11-10 US disclosed
US-20140221667-A1 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2014-08-07 US disclosed
US-8729117-B2 Factor VIIa inhibitor PHARMACYCLICS, INC. (US) 2014-05-20 US disclosed
US-20140080879-A1 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2014-03-20 US disclosed
US-8415328-B2 Factor VIIa inhibitor PHARMACYCLICS, INC (US) 2013-04-09 US disclosed
US-20110207939-A1 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2011-08-25 US disclosed
US-20080275250-A1 Factor Viia Inhibitor PHARMACYCLICS, INC. (US) 2008-11-06 US disclosed
US-20080242644-A1 Factor Viia Inhibitor PHARMACYCLICS, INC. (US) 2008-10-02 US disclosed
EP-1761504-A2 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2007-03-14 EP disclosed
EP-1751114-A2 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2007-02-14 EP disclosed
WO-2005121102-A2 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2005-12-22 WO disclosed
WO-2005118554-A2 FACTOR VIIA INHIBITOR PHARMACYCLICS, INC. (US) 2005-12-15 WO disclosed
WO-1999026932-A1 BY AMIDINO GROUP SUBSTITUTED HETEROCYCLIC DERIVATIVES AND THEIR USE AS ANTICOAGULANTS AXYS PHARMACEUTICALS, INC. (US) 1999-06-03 WO disclosed
EP-0009163-B1 Substituted bisbenzimidazole derivatives, their preparation and antiprotozoic and antiviral agents HOECHST AKTIENGESELLSCHAFT (DE) 1982-06-30 EP disclosed
EP-0009163-A2 Substituted bisbenzimidazole derivatives, their preparation and antiprotozoic and antiviral agents HOECHST AKTIENGESELLSCHAFT (DE) 1980-04-02 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 (5 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-20080242644-A1 Factor Viia Inhibitor F7, F9, F5 PARP1 2090/4885LMNA 534/4885PRSS1 231/4885
US-20110207939-A1 FACTOR VIIA INHIBITOR F7, F9, F5 PARP1 2090/4885LMNA 534/4885PRSS1 231/4885
US-20140080879-A1 FACTOR VIIA INHIBITOR F7, F9, F5 PARP1 2090/4885LMNA 534/4885PRSS1 231/4885
US-20140221667-A1 FACTOR VIIA INHIBITOR F7, F9, F5 PARP1 2090/4885LMNA 534/4885PRSS1 231/4885
US-20080275250-A1 Factor Viia Inhibitor F7, F9, F5 PARP1 2086/4885LMNA 552/4885PRSS1 231/4885

“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.