Indole

Indole

SCHEMBL2796776

Cl.Cl.Cl.c1ccc2[nH]ccc2c1

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 Indole. 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 1/20 0.94
PARP1 known ✓ P09874 1/20 0.44
GAA known ✓ P10253 1/20 0.44
IMPDH2 known ✓ P12268 1/20 0.40
IMPDH1 known ✓ P20839 1/20 0.40
AHR P35869 7/20 0.94
CA1 P00915 2/20 0.94
CA4 P22748 2/20 0.94
CA6 P23280 2/20 0.94
TRPA1 O75762 1/20 0.94
ITGB2 P05107 1/20 0.94
ICAM1 P05362 1/20 0.94
ITGAL P20701 1/20 0.94
ADK P55263 1/20 0.94
NPC1 O15118 1/20 0.50
ALDH1A1 P00352 1/20 0.46
CYP2A6 P11509 3/20 0.44
NR4A2 P43354 2/20 0.44
CMA1 P23946 1/20 0.44
F7 P08709 1/20 0.44

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
Indole SCHEMBL29646222 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL10464295 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL30172823 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL1354880 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL7562348 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL29418280 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL1475229 1.00 AHR (0.94) AHRCA1CA4CA6TRPA1
Indole SCHEMBL23704202 0.97 AHR (0.90) AHRCA1CA4CA6TRPA1
Indole SCHEMBL29800701 0.97 AHR (0.90) AHRCA1CA4CA6TRPA1
Indole SCHEMBL9215713 0.97 AHR (0.90) AHRCA1CA4CA6TRPA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2290877-A None JP disclosed
US-8247407-B2 Pharmaceutical composition with anti-diabetic action Zakrytoe Artsionernoe Obschestvo “Masterclone” (RU) 2012-08-21 US disclosed
US-20100168092-A1 PHARMACEUTICAL COMPOSITION WITH ANTI-DIABETIC ACTION ZAKRYTOE ARTSINONEMOE OBSCHESTO "MASTERCLONE" 2010-07-01 US disclosed
EP-0392913-B1 (3-Diethylaminopropyl)-1-amino-5-methyldipyrido [4,3-b] [3,4-f] indole trihydrochloride ELF SANOFI (FR) 1993-06-23 EP disclosed
JP-H02290877-A 1-(3-DIETHYLAMINOPROPYL)AMINO-5-METHYLDIPYRIDO (4,3-B) (3,4-F1 INDOLE TRIHYDROCHLORIDE SANOFI SA 1990-11-30 JP disclosed
EP-0392913-A1 (3-Diethylaminopropyl)-1-amino-5-methyldipyrido [4,3-b] [3,4-f] indole trihydrochloride ELF SANOFI (FR) 1990-10-17 EP 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 (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-20100168092-A1 PHARMACEUTICAL COMPOSITION WITH ANTI-DIABETIC ACTION IAPP, GPR119, PNLIP CA2 2196/4885PARP1 3102/4885GAA 667/4885

“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.