Trientine

Trientine

SCHEMBL205201

Cl.NCCNCCNCCN

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 Trientine. 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
CA2 known ✓ P00918 4/20 0.92
ESR1 known ✓ P03372 1/20 0.45
KDM4E B2RXH2 1/20 1.00
CA12 O43570 5/20 0.92
CA6 P23280 5/20 0.92
CA7 P43166 5/20 0.92
CA9 Q16790 5/20 0.92
CA14 Q9ULX7 5/20 0.92
CA5B Q9Y2D0 5/20 0.92
CA4 P22748 4/20 0.92
CA5A P35218 4/20 0.92
LMNA P02545 3/20 0.92
TDP1 Q9NUW8 3/20 0.92
CA3 P07451 3/20 0.92
ALOX15 P16050 3/20 0.92
CA1 P00915 2/20 0.92
ALDH1A1 P00352 1/20 0.92
TP53 P04637 1/20 0.92
MEN1 O00255 2/20 0.83
RECQL P46063 2/20 0.83

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 SCHEMBL28797750 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Hydrochloric Acid SCHEMBL285388 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Trientine SCHEMBL506113 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Hydrochloric Acid SCHEMBL284758 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Trientine SCHEMBL2027642 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Trientine SCHEMBL505712 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Trientine SCHEMBL506189 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Hydrochloric Acid SCHEMBL1625351 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Hydrochloric Acid SCHEMBL1626082 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9
Hydrochloric Acid SCHEMBL28797761 1.00 KDM4E (1.00) KDM4ECA12CA6CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4688828-A1 RADIOPHARMACEUTICAL CONJUGATE COMPOUND FOR DIAGNOSIS AND/OR THERAPEUTIC USES THEREOF Jubilant DraxImage Inc. (CA) 2026-02-11 EP claimed
US-12539339-B2 Radiopharmaceutical conjugate compound for diagnosis and/or therapeutic uses thereof JUBILANT DRAXIMAGE INC. (IN) 2026-02-03 US claimed
WO-2025099636-A1 ALBUMIN CONJUGATES AND RADIOPHARMACEUTICAL COMPOSITIONS THEREOF JUBILANT DRAXIMAGE INC (CA) 2025-05-15 WO claimed
US-20250144254-A1 ALBUMIN CONJUGATES AND RADIOPHARMACEUTICAL COMPOSITION THEREOF JUBILANT DRAXIMAGE INC. (CA) 2025-05-08 US claimed
WO-2024201255-A1 RADIOPHARMACEUTICAL CONJUGATE COMPOUND FOR DIAGNOSIS AND/OR THERAPEUTIC USES THEREOF JUBILANT DRAXIMAGE INC. (CA) 2024-10-03 WO claimed
US-20240316226-A1 RADIOPHARMACEUTICAL CONJUGATE COMPOUND FOR DIAGNOSIS AND/OR THERAPEUTIC USES THEREOF JUBILANT DRAXIMAGE INC. (CA) 2024-09-26 US claimed
CN-118562473-A Double-layer coated microcapsule corrosion inhibitor for oil and gas field and preparation method thereof 中国石油天然气股份有限公司 2024-08-30 CN claimed
EP-4210751-A1 ANTI-CERULOPLASMIN ANTIBODIES AND USES THEREOF Alexion Pharmaceuticals, Inc. (US) 2023-07-19 EP claimed
US-20220334135-A1 METHODS OF MEASURING COPPER CONCENTRATION IN BIOLOGICAL SAMPLES ALEXION PHARMACEUTICALS, INC. (US) 2022-10-20 US claimed
CN-110448994-B Process method for trapping NO by using renewable amino functional eutectic solvent 北京化工大学 2022-08-05 CN claimed
EP-1069821-A4 METHOD OF CONTROLLING PROLIFERATION AND DIFFERENTIATION OF STEM AND PROGENITOR CELLS GAMIDA CELL LTD (IL) 2001-11-21 EP claimed
EP-1119345-A1 ENCAPSULATION OF SENSITIVE LIQUID COMPONENTS INTO A MATRIX TO OBTAIN DISCRETE SHELF-STABLE PARTICLES GENERAL MILLS, INC. (US) 2001-08-01 EP claimed
EP-1117762-A1 METHODS OF CONTROLLING PROLIFERATION AND DIFFERENTIATION OF STEM AND PROGENITOR CELLS Gamida Cell Ltd. (IL) 2001-07-25 EP claimed
EP-1069821-A1 METHOD OF CONTROLLING PROLIFERATION AND DIFFERENTIATION OF STEM AND PROGENITOR CELLS Gamida Cell Ltd. (IL) 2001-01-24 EP claimed
WO-2000021504-A1 ENCAPSULATION OF SENSITIVE LIQUID COMPONENTS INTO A MATRIX TO OBTAIN DISCRETE SHELF-STABLE PARTICLES GENERAL MILLS, INC. (US) 2000-04-20 WO claimed
WO-2000018885-A1 METHODS OF CONTROLLING PROLIFERATION AND DIFFERENTIATION OF STEM AND PROGENITOR CELLS GAMIDA CELL LTD. (IL) 2000-04-06 WO claimed
EP-0935523-A4 EMBEDDING AND ENCAPSULATION OF CONTROLLED RELEASE PARTICLES GEN MILLS INC (US) 1999-12-29 EP claimed
WO-1999040783-A1 METHOD OF CONTROLLING PROLIFERATION AND DIFFERENTIATION OF STEM AND PROGENITOR CELLS GAMIDA CELL LTD. (IL) 1999-08-19 WO claimed
EP-0935523-A1 EMBEDDING AND ENCAPSULATION OF CONTROLLED RELEASE PARTICLES GENERAL MILLS, INC. (US) 1999-08-18 EP claimed
WO-1998018610-A1 EMBEDDING AND ENCAPSULATION OF CONTROLLED RELEASE PARTICLES LENGERICH BERNHARD H VAN (US) 1998-05-07 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-12539339-B2 Radiopharmaceutical conjugate compound for diagnosis and/or therapeutic uses thereof SLC7A1, SLC39A11, SLC39A3 CA2 253/4885ESR1 3148/4885KDM4E 1420/4885

“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.