Abrine (L)

Abrine (L)

SCHEMBL5056403

CNC(Cc1c[nH]c2ccccc12)C(=O)O.Cl

nearest known ligand 0.69

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 Abrine (L). 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
ACE known ✓ P12821 3/20 0.67
ALOX15 P16050 1/20 0.69
KDM4E B2RXH2 2/20 0.66
MAPT P10636 2/20 0.66
APAF1 O14727 1/20 0.66
POLB P06746 1/20 0.66
RECQL P46063 1/20 0.66
L3MBTL1 Q9Y468 1/20 0.66
ITGB2 P05107 3/20 0.65
ICAM1 P05362 3/20 0.65
ITGAL P20701 3/20 0.65
SMN1; SMN2 Q16637 1/20 0.63
ECE1 P42892 4/20 0.62
MEN1 O00255 1/20 0.62
LMNA P02545 1/20 0.62
MPO P05164 1/20 0.62
TSHR P16473 1/20 0.62
BLM P54132 1/20 0.62
PMP22 Q01453 1/20 0.62
KMT2A Q03164 1/20 0.62

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
Abrine SCHEMBL5056408 1.00 ALOX15 (0.69) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL23668057 1.00 ALOX15 (0.69) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL161767 0.99 ALOX15 (0.70) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL29404678 0.99 ALOX15 (0.70) ALOX15ACEKDM4EMAPTAPAF1
Abrine (L) SCHEMBL18777 0.99 ALOX15 (0.70) ALOX15ACEKDM4EMAPTAPAF1
Abrine (L) SCHEMBL29585648 0.99 ALOX15 (0.70) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL18778 0.99 ALOX15 (0.70) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL30320025 0.97 ALOX15 (0.69) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL8871893 0.97 ALOX15 (0.69) ALOX15ACEKDM4EMAPTAPAF1
Abrine SCHEMBL30413313 0.97 ALOX15 (0.69) ALOX15ACEKDM4EMAPTAPAF1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1926466-A2 STABLE EMULSION SYSTEMS WITH HIGH SALT TOLERANCE COMBE INCORPORATED (US) 2008-06-04 EP claimed
WO-2007040598-A2 STABLE EMULSION SYSTEMS WITH HIGH SALT TOLERANCE COMBE INCORPORATED (US) 2007-04-12 WO claimed
US-20070065390-A1 Stable emulsion systems with high salt tolerance RECKITT BENCKISER LLC 2007-03-22 US claimed
CN-112961096-B Chalcone tryptophan derivatives with cisplatin nephrotoxicity and antitumor activity 安徽医科大学 2023-05-30 CN disclosed
CN-112961096-A Chalcone tryptophan derivatives with improved cisplatin nephrotoxicity and antitumor activity 安徽医科大学 2021-06-15 CN disclosed
CN-110156846-A A kind of preparation process of D-galactosamine hydrochloride 南京博源医药科技有限公司 2019-08-23 CN disclosed
EP-1926466-A2 STABLE EMULSION SYSTEMS WITH HIGH SALT TOLERANCE COMBE INCORPORATED (US) 2008-06-04 EP disclosed
WO-2007040598-A2 STABLE EMULSION SYSTEMS WITH HIGH SALT TOLERANCE COMBE INCORPORATED (US) 2007-04-12 WO disclosed
US-20070065390-A1 Stable emulsion systems with high salt tolerance RECKITT BENCKISER LLC 2007-03-22 US disclosed
EP-0227787-B1 PRODUCTION OF INDOLE ALPHA-KETOACIDS FROM ALPHA-AMINOACID, PARTICULARLY OF INDOLEPYRUVIC ACID POLIFARMA S.p.A. (IT) 1990-08-29 EP disclosed
EP-0227787-A1 PRODUCTION OF INDOLE ALPHA-KETOACIDS FROM ALPHA-AMINOACID, PARTICULARLY OF INDOLEPYRUVIC ACID. POLIFARMA SPA (IT) 1987-07-08 EP disclosed
WO-1987000169-A1 PRODUCTION OF INDOLE ALPHA-KETOACIDS FROM ALPHA-AMINOACID, PARTICULARLY OF INDOLEPYRUVIC ACID POLIFARMA S.P.A. (IT) 1987-01-15 WO disclosed