Pi-Clonidine

Pi-Clonidine

SCHEMBL5274141

Cl.Clc1cc(I)cc(Cl)c1NC1=NCCN1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 Pi-Clonidine. 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
ADRA2A known ✓ P08913 9/20 0.97
ADRA2B known ✓ P18089 8/20 0.97
ADRA2C known ✓ P18825 8/20 0.97
HTR1D known ✓ P28221 4/20 0.97
HTR1B known ✓ P28222 3/20 0.97
ADRA1A known ✓ P35348 4/20 0.69
ADRA1D known ✓ P25100 3/20 0.69
ADRA1B known ✓ P35368 3/20 0.69
HTR2A known ✓ P28223 1/20 0.67
HTR2C known ✓ P28335 1/20 0.67
HTR7 known ✓ P34969 1/20 0.67
HRH2 known ✓ P25021 2/20 0.64
HTR1A known ✓ P08908 1/20 0.64
OPRK1 known ✓ P41145 1/20 0.64
CFB known ✓ P00751 2/20 0.56
LMNA P02545 5/20 1.00
BLM P54132 3/20 1.00
CYP2D6 P10635 3/20 0.97
NISCH Q9Y2I1 3/20 0.97
CYP1A2 P05177 1/20 0.97

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
Pi-Clonidine SCHEMBL563884 0.98 ADRA2A (1.00) LMNABLMADRA2AADRA2BADRA2C
SCHEMBL11180812 0.85 ADRA2A (0.76) LMNABLMADRA2AADRA2BADRA2C
Apraclonidine SCHEMBL1002875 0.84 BLM (1.00) LMNABLMADRA2AADRA2BADRA2C
SCHEMBL24658874 0.82 ADRA2A (0.71) LMNABLMADRA2AADRA2BADRA2C
Apraclonidine SCHEMBL34128 0.82 ADRA2A (1.00) LMNABLMADRA2AADRA2BADRA2C
SCHEMBL10414088 0.82 ADRA2A (0.71) LMNABLMADRA2AADRA2BADRA2C
Apraclonidine SCHEMBL1649431 0.81 ADRA2A (0.97) LMNABLMADRA2AADRA2BADRA2C
Bromide SCHEMBL11608848 0.81 ADRA2A (0.69) LMNABLMADRA2AADRA2BADRA2C
Clonidine SCHEMBL2231324 0.80 ADRA2A (1.00) LMNABLMADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL1322022 0.79 LMNA (0.69) LMNABLMADRA2AADRA2BADRA2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1776955-B1 Medical use and composition for the treatment of lipid and glucose metabolism disorders VEROSCIENCE LLC (US) 2012-08-15 EP disclosed
EP-1776955-A1 Method and composition for the treatment of lipid and glucose metabolism disorders PLIVA D.D. (HR) 2007-04-25 EP disclosed
US-6855707-B2 Method for the treatment of lipid and glucose metabolism disorders PLIVA D.D. (HR) 2005-02-15 US disclosed
US-20030147899-A1 Endogenous hormone adjuvant and uses thereof DHABHAR FIRDAUS S (US) 2003-08-07 US disclosed
US-20030050226-A1 Dopamine analog amide SHASHOUA VICTOR E (US) 2003-03-13 US disclosed
US-20020187985-A1 Method and composition for the treatment of lipid and glucose metabolism disorders VEROSCIENCE LLC 2002-12-12 US disclosed
US-6407137-B2 A PRODRUG COMPOUND CAPABLE OF FACILITATING THE PASSAGE OF A DRUG ACROSS THE BLOOD BRAIN BARRIER COMPRISING A FATTY ACID COUPLED TO A DRUG TO FORM A PRODRUG PROTARGA, INC. 2002-06-18 US disclosed
US-20010056116-A1 Dopamine analog amide LUITPOLD PHARMACEUTICALS, INC. 2001-12-27 US disclosed
US-20010016582-A1 METHOD AND COMPOSITION FOR THE TREATMENT OF LIPID AND GLUCOSE METABOLISM DISORDERS CINCOTTA ANTHONY H (US) 2001-08-23 US disclosed
US-6258836-B1 FATTY ACID COUPLED TO ANTIAIDS SUBSTANCE, ANTIBIOTIC, CHOLINERGIC AGONIST AND OTHER USES FOR PASSING THE BLOOD BRAIN BARRIER PROTARGA, INC. 2001-07-10 US disclosed
US-6107499-A FACILITATING THE TRANSPORT OF A NEUROTRANSMITTER ACROSS THE BLOOD BRAIN BARRIER BY ADMINISTERING THE DRUG, A NEUROTRANSMITTER SUCH AS DOPAMINE COVALENTLY COUPLED TO A SINGLE, STRAIGHT-CHAINED FATTY ACID CARRIER MOLECULE NEUROMEDICA, INC. (US) 2000-08-22 US disclosed
US-5994392-A PASSAGE OF DRUG THROUGH BLOOD BRAIN BARRIER NEUROMEDICA, INC. (US) 1999-11-30 US disclosed
US-5877183-A Treatment of lipid and glucose metabolism disorders with dopamine and serotonin agonists ERGO RESEARCH CORPORATION (US) 1999-03-02 US disclosed
WO-1997046239-A1 TREATMENT OF LIPID AND GLUCOSE METABOLISM DISORDERS WITH DOPAMINE AND SEROTONIN AGONISTS ERGO RESEARCH CORPORATION (US) 1997-12-11 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 (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-20010056116-A1 Dopamine analog amide FABP7, SLC6A3, ALOX15 ADRA2A 100/4885ADRA2B 305/4885ADRA2C 260/4885
US-20030050226-A1 Dopamine analog amide FABP7, SLC6A3, ALOX15 ADRA2A 100/4885ADRA2B 305/4885ADRA2C 260/4885

“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.