SCHEMBL60730

SCHEMBL60730

c1ccc2ccc3nc4ccccc4c3c2nc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.55
CYP3A4 P08684 2/20 0.47
KDM4E B2RXH2 5/20 0.47
SMN1; SMN2 Q16637 5/20 0.47
MAPT P10636 5/20 0.47
TDP1 Q9NUW8 3/20 0.47
TP53 P04637 2/20 0.47
CCR1 P32246 2/20 0.47
CCR5 P51681 2/20 0.47
CCR8 P51685 2/20 0.47
HTT P42858 2/20 0.47
HIF1A Q16665 2/20 0.47
GMNN O75496 1/20 0.47
HSP90AA1 P07900 1/20 0.47
MMP2 P08253 1/20 0.47
CYP2D6 P10635 1/20 0.47
MMP9 P14780 1/20 0.47
ALOX15 P16050 1/20 0.47
TSHR P16473 1/20 0.47
NFKB1 P19838 1/20 0.47

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
SCHEMBL9394726 0.86 LMNA (0.45) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL30311893 0.79 LMNA (0.43) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL10623725 0.79 LMNA (0.43) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL29687953 0.77 LMNA (0.58) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL982910 0.77 LMNA (0.58) LMNACYP3A4KDM4ESMN1; SMN2MAPT
Phenazine SCHEMBL5691639 0.76 LMNA (0.85) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL28399164 0.76 LMNA (0.56) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL6032927 0.75 LMNA (0.59) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL18748071 0.75 LMNA (0.54) LMNACYP3A4KDM4ESMN1; SMN2MAPT
SCHEMBL17422697 0.73 CYP3A4 (0.54) LMNACYP3A4KDM4ESMN1; SMN2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122081965-A Synthesis method and application of electrochemical promotion of indolobenzselenazepine ketone compound 2026-05-26 CN disclosed
EP-2822943-B1 PHOSPHOINOSITIDE 3-KINASE INHIBITORS KARUS THERAPEUTICS LTD (GB) 2018-10-03 EP disclosed
EP-2310396-B1 MACROCYCLIC INDOLE DERIVATIVES USEFUL AS HEPATITIS C VIRUS INHIBITORS JANSSEN SCIENCES IRELAND UC (IE) 2017-09-06 EP disclosed
EP-2099804-B1 COMPOUNDS FOR THE TREATMENT OF HEPATITIS C BRISTOL MYERS SQUIBB CO (US) 2017-03-22 EP disclosed
US-9427440-B2 Macrocyclic indole derivatives useful as hepatitis C virus inhibitors JANSSEN SCIENCES IRELAND UC (IE) 2016-08-30 US disclosed
EP-2518073-B1 Compounds for the treatment of Hepatitis C BRISTOL MYERS SQUIBB CO (US) 2015-08-26 EP disclosed
US-8921355-B2 Macrocyclic indole derivatives useful as hepatitis C virus inhibitors JANSSEN R & D IRELAND (IE) 2014-12-30 US disclosed
EP-2118109-B1 COMPOUNDS FOR THE TREATMENT OF HEPATITIS C BRISTOL MYERS SQUIBB CO (US) 2014-11-26 EP disclosed
US-20140186299-A1 Cyclopropyl Fused Indolobenzazepine HCV NS5B Inhibitors BRISTOL MYERS SQUIBB CO (US) 2014-07-03 US disclosed
US-20140186299-A1 Cyclopropyl Fused Indolobenzazepine HCV NS5B Inhibitors BRISTOL MYERS SQUIBB CO (US) 2014-07-03 US disclosed
US-7153848-B2 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY (US) 2006-12-26 US disclosed
US-20060166964-A1 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY 2006-07-27 US disclosed
US-20060046983-A1 Inhibitors of HCV replication BRISTOL-MYERS SQUIBB COMPANY 2006-03-02 US disclosed
WO-2006020082-A1 INHIBITORS OF HCV REPLICATION BRISTOL-MYERS SQUIBB COMPANY (US) 2006-02-23 WO disclosed
US-4070467-A Trans-octahydro-pyrido-indolo-benzazepine-3-alkanols, -alkanonitriles,-alkanoic acid and ester as tranquilizers ENDO LABORATORIES, INC. (US) 1978-01-24 US disclosed
US-4018930-A ANALGESICS, SEDATIVES, TRANQUILIZERS ENDO LABORATORIES, INC. (US) 1977-04-19 US disclosed
US-3989717-A ANTIDEPRESSANTS HOFFMANN-LA ROCHE INC. (US) 1976-11-02 US disclosed
US-3989717-A ANTIDEPRESSANTS HOFFMANN-LA ROCHE INC. (US) 1976-11-02 US disclosed
US-3959300-A Novel indolobenzazepine derivatives, useful as tranquilizers ENDO LABORATORIES, INC. (US) 1976-05-25 US disclosed
US-3959300-A Novel indolobenzazepine derivatives, useful as tranquilizers ENDO LABORATORIES, INC. (US) 1976-05-25 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 (3 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-20140186299-A1 Cyclopropyl Fused Indolobenzazepine HCV NS5B Inhibitors HAVCR2, ZC3HAV1, HCCS LMNA 3938/4885CYP3A4 54/4885KDM4E 1448/4885
US-20060166964-A1 Inhibitors of HCV replication EIF2AK2, HCCS, IDO1 LMNA 3453/4885CYP3A4 500/4885KDM4E 2251/4885
US-20060046983-A1 Inhibitors of HCV replication EIF2AK2, HCCS, IDO1 LMNA 3453/4885CYP3A4 500/4885KDM4E 2251/4885

“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.