Acridine

Acridine

SCHEMBL96928

Cl.Cl.c1ccc2nc3ccccc3cc2c1

nearest known ligand 0.94

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 Acridine. 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
GLA known ✓ P06280 2/20 0.94
ACHE known ✓ P22303 1/20 0.94
HTR3A known ✓ P46098 1/20 0.62
GAA known ✓ P10253 2/20 0.54
CACNA1B known ✓ Q00975 1/20 0.48
MAPT P10636 3/20 0.94
ALDH1A1 P00352 3/20 0.94
HPGD P15428 3/20 0.94
NQO2 P16083 2/20 0.60
KMT2A Q03164 3/20 0.54
KDM4E B2RXH2 2/20 0.54
NPC1 O15118 2/20 0.54
POLB P06746 2/20 0.54
RAB9A P51151 2/20 0.54
LMNA P02545 1/20 0.54
PTBP1 P26599 1/20 0.54
RCE1 Q9Y256 1/20 0.54
TDP1 Q9NUW8 1/20 0.50
STAT3 P40763 1/20 0.50
MEN1 O00255 1/20 0.48

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
Acridine SCHEMBL30257128 1.00 MAPT (0.94) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL1798660 1.00 MAPT (0.94) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL28062881 0.97 MAPT (0.88) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL4972293 0.97 ALDH1A1 (1.00) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL3045498 0.97 ALDH1A1 (1.00) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL8339 0.97 ALDH1A1 (1.00) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL1772714 0.97 ALDH1A1 (1.00) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL29352289 0.97 ALDH1A1 (1.00) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL1551975 0.94 ALDH1A1 (0.94) MAPTALDH1A1HPGDGLAACHE
Acridine SCHEMBL2401648 0.94 ALDH1A1 (0.94) MAPTALDH1A1HPGDGLAACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260139331-A1 HIGH-THROUGHPUT METHODS FOR ISOLATING AND CHARACTERIZING AMMONIUM-EXCRETING MUTANT LIBRARIES GENERATED BY CHEMICAL MUTAGENESIS PIVOT BIO INC (US) 2026-05-21 US claimed
US-20220282340-A1 HIGH-THROUGHPUT METHODS FOR ISOLATING AND CHARACTERIZING AMMONIUM-EXCRETING MUTANT LIBRARIES GENERATED BY CHEMICAL MUTAGENESIS HSBC BANK USA, N.A. 2022-09-08 US claimed
CN-114008221-A High throughput method for isolating and characterizing pools of ammonium secreting mutants generated by chemical mutagenesis 皮沃特生物股份有限公司 2022-02-01 CN claimed
WO-1999006405-A1 PYRAZOLO-ACRIDINE DERIVATIVES HAVING ANTITUMOUR ACTIVITY UNIVERSITA' DEGLI STUDI DI CAMERINO (IT) 1999-02-11 WO claimed
US-20260139331-A1 HIGH-THROUGHPUT METHODS FOR ISOLATING AND CHARACTERIZING AMMONIUM-EXCRETING MUTANT LIBRARIES GENERATED BY CHEMICAL MUTAGENESIS PIVOT BIO INC (US) 2026-05-21 US disclosed
US-12612669-B2 High-throughput methods for isolating and characterizing ammonium-excreting mutant libraries generated by chemical mutagenesis PIVOT BIO, INC. (US) 2026-04-28 US disclosed
US-12442014-B2 Oomycete resistance in cucumber and tomato NUNHEMS B.V. (NL) 2025-10-14 US disclosed
CN-113924367-B Method for improving rice grain yield 南京农业大学 2024-07-23 CN disclosed
US-11987799-B2 Downy mildew resistance in Cucurbitaceae plants NUNHEMS B.V. (NL) 2024-05-21 US disclosed
CN-115918526-A Haploid inducer compositions and methods of use thereof 先正达参股股份有限公司 2023-04-07 CN disclosed
CN-115915927-A Methods for inducing endogenous tandem replication events 莱顿大学医学中心附属莱顿教学医院 2023-04-04 CN disclosed
US-20220282340-A1 HIGH-THROUGHPUT METHODS FOR ISOLATING AND CHARACTERIZING AMMONIUM-EXCRETING MUTANT LIBRARIES GENERATED BY CHEMICAL MUTAGENESIS HSBC BANK USA, N.A. 2022-09-08 US disclosed
EP-2426205-A1 GENES HOMOLOGOUS TO THE FLOWERING LOCUS T (FT) GENE AND THE USE THEREOF FOR MODULATING TUBERIZATION Consejo Superior de Investigaciones Científicas (CSIC) (ES) 2012-03-07 EP disclosed
CN-1942430-A 5-aminolevulinic acid salts, method for the production thereof and use thereof COSMO OIL CO LTD (JP) 2007-04-04 CN disclosed
CN-1163595-C Process for inactivation of viruses with aid of acridine or acridine derivatives 2004-08-25 CN disclosed
US-5871361-A Educational kit MICROBIX BIOSYSTEMS, INC. (CA) 1999-02-16 US disclosed
WO-1999006405-A1 PYRAZOLO-ACRIDINE DERIVATIVES HAVING ANTITUMOUR ACTIVITY UNIVERSITA' DEGLI STUDI DI CAMERINO (IT) 1999-02-11 WO disclosed
CN-1132249-A Process for inactivation of viruses with aid of acridine or acridine derivatives BEHRINGWERKE AG (DE) 1996-10-02 CN disclosed
US-4244954-A Acridine compounds and methods of combatting viruses with them STERLING DRUG INC. (US) 1981-01-13 US disclosed
US-4150134-A Aminoalkoxy substituted 9(aryl or aralkyl)-acridines STERLING DRUG INC. (US) 1979-04-17 US 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-12612669-B2 High-throughput methods for isolating and characterizing ammonium-excreting mutant libraries generated by chemical mutagenesis QPCTL, GLUL, GFPT1 GLA 2655/4885ACHE 4139/4885HTR3A 4412/4885
US-20260139331-A1 HIGH-THROUGHPUT METHODS FOR ISOLATING AND CHARACTERIZING AMMONIUM-EXCRETING MUTANT LIBRARIES GENERATED BY CHEMICAL MUTAGENESIS GLUL, SPOUT1, QPCTL GLA 2376/4885ACHE 3542/4885HTR3A 4408/4885

“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.