Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1271897

Cl.F/C(COc1ccc2c(c1)[nH]c1ccccc12)=C1/CN2CCC1CC2

nearest known ligand 0.98

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
▸ GABRA1 known ✓ P14867 2/20 0.34
▸ GABRG2 known ✓ P18507 2/20 0.34
▸ GABRB3 known ✓ P28472 2/20 0.34
▸ GABRA3 known ✓ P34903 2/20 0.34
▸ GABRA2 known ✓ P47869 2/20 0.34
▸ GABRP known ✓ O00591 1/20 0.34
▸ GABRD known ✓ O14764 1/20 0.34
▸ GABRB1 known ✓ P18505 1/20 0.34
▸ GABRA5 known ✓ P31644 1/20 0.34
▸ GABRB2 known ✓ P47870 1/20 0.34
▸ GABRA4 known ✓ P48169 1/20 0.34
▸ GABRE known ✓ P78334 1/20 0.34
▸ GABRA6 known ✓ Q16445 1/20 0.34
▸ GABRG1 known ✓ Q8N1C3 1/20 0.34
▸ GABRG3 known ✓ Q99928 1/20 0.34
▸ GABRQ known ✓ Q9UN88 1/20 0.34
▸ GAA known ✓ P10253 1/20 0.33
▸ DRD3 known ✓ P35462 1/20 0.33
▸ HTT P42858 2/20 0.98
▸ THRB P10828 1/20 0.98

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 SCHEMBL1061360 1.00 HTT (0.98) HTTTHRBKIF11CTSVCTSL
Hydrochloric Acid SCHEMBL1271899 1.00 HTT (0.98) HTTTHRBKIF11CTSVCTSL
Hydrochloric Acid SCHEMBL31741907 1.00 HTT (0.98) HTTTHRBKIF11CTSVCTSL
SCHEMBL8248041 0.99 HTT (1.00) HTTTHRBKIF11CTSVCTSL
SCHEMBL29369556 0.99 HTT (1.00) HTTTHRBKIF11CTSVCTSL
SCHEMBL8898611 0.99 HTT (1.00) HTTTHRBKIF11CTSVCTSL
SCHEMBL8898607 0.99 HTT (1.00) HTTTHRBKIF11CTSVCTSL
SCHEMBL8898736 0.98 HTT (0.98) HTTTHRBKIF11CTSVCTSL
Hydrochloric Acid SCHEMBL8900179 0.87 THRB (0.76) HTTTHRBKIF11CTSVCTSL
Hydrochloric Acid SCHEMBL8900181 0.87 THRB (0.76) HTTTHRBKIF11CTSVCTSL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160193231-A1 RETT SYNDROME AND TREATMENTS THEREFORE RETT SYNDROME RES TRUST (US) 2016-07-07 — — US disclosed
US-9297031-B2 Production of carotenoids in oleaginous yeast and fungi DSM IP ASSETS B.V. (NL) 2016-03-29 — — US disclosed
US-20140234928-A1 PRODUCTION OF CAROTENOIDS IN OLEAGINOUS YEAST AND FUNGI DSM IP ASSETS B.V. (NL) 2014-08-21 — — US disclosed
US-20120149886-A1 PRODUCTION OF CAROTENOIDS IN OLEAGINOUS YEAST AND FUNGI MICROBIA, INC. (US) 2012-06-14 — — US disclosed
WO-2011077245-A2 COMPOSITIONS FONDAZIONE CENTRO SAN RAFFAELE DEL MONTE TABOR (IT) 2011-06-30 — — WO disclosed
US-20110039299-A1 PRODUCTION OF CAROTENOIDS IN OLEAGINOUS YEAST AND FUNGI MICROBIA PRECISION ENGINEERING (US) 2011-02-17 — — US disclosed
US-20040102405-A1 Using compounds comprising oligonucleotides targeted to nucleic acid encoding squalene synthase; for diagnosis and treatment of disease associated with expression of squalene synthase; cardiovascular disorders, atherosclerosis ISIS PHARMACEUTICALS INC. 2004-05-27 — — US disclosed
EP-0812840-A1 NOVEL QUINUCLIDINE DERIVATIVES HAVING TRICYCLIC FUSED HETERO RING YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1997-12-17 — — EP disclosed
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