Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2460422

CCCCCCCCCCCCCC(CCCCCCCCCCCC)NC(=O)C(N)C(N)C(=O)[C@@H](N)CCCNC(=N)N.Cl.Cl.Cl

nearest known ligand 0.48

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
RRM1 known ✓ P23921 1/20 0.44
DPP4 known ✓ P27487 1/20 0.36
S1PR2 known ✓ O95136 1/20 0.35
S1PR1 known ✓ P21453 1/20 0.35
S1PR3 known ✓ Q99500 1/20 0.35
S1PR5 known ✓ Q9H228 1/20 0.35
GNAI3 P08754 1/20 0.48
GNAO1 P09471 1/20 0.48
GNAI1 P63096 1/20 0.48
DPP7 Q9UHL4 3/20 0.47
NOD1 Q9Y239 2/20 0.39
NPY4R P50391 6/20 0.38
NPY1R P25929 5/20 0.38
NPY2R P49146 4/20 0.38
NPY5R Q15761 4/20 0.38
SIRT6 Q8N6T7 1/20 0.37
SIRT1 Q96EB6 1/20 0.37
TLR2 O60603 1/20 0.36
SPHK1 Q9NYA1 3/20 0.36
DPP8 Q6V1X1 1/20 0.36

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
SCHEMBL446551 0.99 GNAI3 (0.49) GNAI3GNAO1GNAI1DPP7RRM1
Hydrochloric Acid SCHEMBL446543 0.91 GNAI3 (0.50) GNAI3GNAO1GNAI1DPP7RRM1
SCHEMBL14627405 0.89 GNAI3 (0.51) GNAI3GNAO1GNAI1DPP7RRM1
Hydrochloric Acid SCHEMBL5540410 0.88 GNAI3 (0.52) GNAI3GNAO1GNAI1DPP7RRM1
SCHEMBL16209914 0.83 GNAI3 (0.57) GNAI3GNAO1GNAI1DPP7RRM1
SCHEMBL25670816 0.80 GNAI3 (0.50) GNAI3GNAO1GNAI1DPP7RRM1
SCHEMBL24420660 0.80 DPP7 (0.73) GNAI3GNAO1GNAI1DPP7RRM1
SCHEMBL27115127 0.80 DPP7 (0.73) GNAI3GNAO1GNAI1DPP7RRM1
Hydrochloric Acid SCHEMBL3486209 0.79 DPP7 (0.41) GNAI3GNAO1GNAI1DPP7RRM1
Hydrochloric Acid SCHEMBL27908684 0.79 DPP7 (0.41) GNAI3GNAO1GNAI1DPP7RRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1771206-B1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS GMBH (DE) 2018-04-11 EP disclosed
US-20170036990-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS AG (DE) 2017-02-09 US disclosed
US-9486538-B2 Lipids, lipid complexes and use thereof SILENCE THERAPEUTICS GMBH (DE) 2016-11-08 US disclosed
US-9387262-B2 Coated lipid complexes and their use SILENCE THERAPEUTICS GMBH (DE) 2016-07-12 US disclosed
EP-2992902-A1 LIPID COMPLEXES COATED WITH PEG AND THEIR USES Silence Therapeutics GmbH (DE) 2016-03-09 EP disclosed
US-20150359906-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS AG (DE) 2015-12-17 US disclosed
US-9125820-B2 Lipids, lipid complexes and use thereof SILENCE THERAPEUTICS GMBH (DE) 2015-09-08 US disclosed
US-20150031752-A1 COATED LIPID COMPLEXES AND THEIR USE SILENCE THERAPEUTICS AG (DE) 2015-01-29 US disclosed
US-20140329885-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS GMBH (DE) 2014-11-06 US disclosed
US-8852472-B2 Coated lipid complexes and their use SILENCE THERAPEUTICS GMBH (DE) 2014-10-07 US disclosed
US-8735453-B2 Lipids, lipid complexes and use thereof SILENCE THERAPEUTICS GMBH (DE) 2014-05-27 US disclosed
US-20130165381-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS AG (DE) 2013-06-27 US disclosed
US-8357722-B2 Lipids, lipid complexes and use thereof Silence Therpeutics AG (DE) 2013-01-22 US disclosed
US-20110294871-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF SILENCE THERAPEUTICS AG (DE) 2011-12-01 US disclosed
US-8017804-B2 Lipids, lipid complexes and use thereof SILENCE THERAPEUTICS AG (DE) 2011-09-13 US disclosed
US-20100062967-A1 COATED LIPID COMPLEXES AND THEIR USE SILENCE THERAPEUTICS AG (DE) 2010-03-11 US disclosed
US-20080274116-A1 Lipids, Lipid Complexes and Use Thereof SILENCE THERAPEUTICS AG (DE) 2008-11-06 US disclosed
EP-1771206-A2 LIPIDS, LIPID COMPLEXES AND USE THEREOF atugen AG (DE) 2007-04-11 EP disclosed
WO-2005105152-A2 LIPIDS, LIPID COMPLEXES AND USE THEREOF ATUGEN AG (DE) 2005-11-10 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 (8 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-20110294871-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF MGLL, LIPA, SGMS1 RRM1 2729/4885DPP4 345/4885S1PR2 127/4885
US-20130165381-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF MGLL, LIPA, LIPC RRM1 2846/4885DPP4 223/4885S1PR2 173/4885
US-20100062967-A1 COATED LIPID COMPLEXES AND THEIR USE HDLBP, NR1H3, CETP RRM1 4043/4885DPP4 2985/4885S1PR2 575/4885
US-20170036990-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF MGLL, LIPA, LIPC RRM1 2846/4885DPP4 223/4885S1PR2 173/4885
US-20150359906-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF MGLL, LIPA, LIPC RRM1 2846/4885DPP4 223/4885S1PR2 173/4885
US-20150031752-A1 COATED LIPID COMPLEXES AND THEIR USE HDLBP, NR1H3, CETP RRM1 4043/4885DPP4 2985/4885S1PR2 575/4885
US-20080274116-A1 Lipids, Lipid Complexes and Use Thereof MGLL, LIPA, SGMS1 RRM1 2638/4885DPP4 346/4885S1PR2 128/4885
US-20140329885-A1 LIPIDS, LIPID COMPLEXES AND USE THEREOF MGLL, LIPA, LIPC RRM1 2846/4885DPP4 223/4885S1PR2 173/4885

“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.