SCHEMBL5511518

SCHEMBL5511518

COc1ccc(Cl)c(NCc2ccccc2)c1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.57
HDAC1 Q13547 1/20 0.52
HDAC8 Q9BY41 1/20 0.52
HDAC6 Q9UBN7 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
TACR3 P29371 1/20 0.52
ACP1 P24666 3/20 0.50
RAB9A P51151 2/20 0.49
EGFR P00533 2/20 0.49
TP53 P04637 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
NPC1 O15118 1/20 0.49
ABCB1 P08183 1/20 0.49
ABCG2 Q9UNQ0 1/20 0.49
P2RX7 Q99572 1/20 0.48
DRD2 P14416 1/20 0.48
DRD3 P35462 1/20 0.48
NCF1 P14598 1/20 0.48
MAPT P10636 2/20 0.48
MEN1 O00255 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
SCHEMBL5436700 0.88 TACR3 (0.52) L3MBTL1TACR3ACP1RAB9AEGFR
SCHEMBL30691740 0.83 HDAC8 (0.60) TDP1HDAC1HDAC8HDAC6L3MBTL1
SCHEMBL8557712 0.83 HDAC1 (0.54) HDAC1HDAC8HDAC6L3MBTL1TACR3
SCHEMBL6689330 0.81 LMNA (0.55) HDAC1HDAC8HDAC6L3MBTL1TACR3
SCHEMBL6814420 0.81 NCF1 (0.54) HDAC1L3MBTL1TACR3ACP1RAB9A
SCHEMBL5436695 0.81 POLB (0.55) TDP1L3MBTL1ACP1RAB9ANPC1
SCHEMBL413427 0.80 TDP1 (0.56) TDP1L3MBTL1ACP1SMN1; SMN2P2RX7
SCHEMBL11037476 0.79 GAA (0.59) L3MBTL1TACR3ACP1RAB9AEGFR
SCHEMBL10787691 0.79 RAB9A (0.55) TACR3ACP1RAB9AEGFRTP53
SCHEMBL11510637 0.78 HDAC1 (0.59) HDAC1HDAC8HDAC6L3MBTL1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119039158-A Preparation method of aromatic amine compound 浙江工业大学 2024-11-29 CN disclosed
US-9475769-B2 Zinc halide mediated cyclization process leading to tricyclic indoles GE HEALTHCARE LIMITED (GB) 2016-10-25 US disclosed
US-9475769-B2 Zinc halide mediated cyclization process leading to tricyclic indoles GE HEALTHCARE LIMITED (GB) 2016-10-25 US disclosed
US-9475769-B2 Zinc halide mediated cyclization process leading to tricyclic indoles GE HEALTHCARE LIMITED (GB) 2016-10-25 US disclosed
US-20150336891-A1 Zinc Halide Mediated Cyclization Process Leading to Tricyclic Indoles GE HEALTHCARE LIMITED (GB) 2015-11-26 US disclosed
US-20150336891-A1 Zinc Halide Mediated Cyclization Process Leading to Tricyclic Indoles GE HEALTHCARE LIMITED (GB) 2015-11-26 US disclosed
US-20150336891-A1 Zinc Halide Mediated Cyclization Process Leading to Tricyclic Indoles GE HEALTHCARE LIMITED (GB) 2015-11-26 US disclosed
EP-2925723-A1 ZINC HALIDE MEDIATED CYCLIZATION PROCESS LEADING TO TRICYCLIC INDOLES GE Healthcare Limited (GB) 2015-10-07 EP disclosed
WO-2014083163-A1 ZINC HALIDE MEDIATED CYCLIZATION PROCESS LEADING TO TRICYCLIC INDOLES GE HEALTHCARE LIMITED (GB) 2014-06-05 WO disclosed
US-7160909-B2 Cyclopenta[b]indole derivatives as sPLA2 inhibitors ELI LILLY AND COMPANY (US) 2007-01-09 US disclosed
EP-1438290-B1 CYCLOHEPT B!INDOLE DERIVATIVES AS SPLA2 INHIBITORS LILLY CO ELI (US) 2005-12-14 EP disclosed
US-20050026988-A1 Cyclopenta'b! indole derivatives as spla inhibitors KINNICK MICHAEL DEAN (US) 2005-02-03 US disclosed
US-20040198801-A1 Cyclohept'b!indole derivatives as spla2 inhibitors KINNICK MICHAEL DEAN (US) 2004-10-07 US disclosed
EP-1438290-A1 CYCLOHEPT B!INDOLE DERIVATIVES AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2004-07-21 EP disclosed
EP-0952149-B1 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitiors LILLY CO ELI (US) 2004-06-09 EP disclosed
US-6713645-B1 INHIBITING SPLA2 MEDIATED RELEASE OF FATTY ACIDS FOR TREATMENT OF CONDITIONS SUCH AS SEPTIC SHOCK ELI LILLY AND COMPANY 2004-03-30 US disclosed
WO-2003016277-A1 CYCLOHEPT`B!INDOLE DERIVATIVES AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2003-02-27 WO disclosed
US-6177440-B1 THERAPY FOR SEPSIS SHOCK; PHOSPHOLIPASE INHBITOR ELI LILLY AND COMPANY 2001-01-23 US disclosed
CN-1240210-A Substituted tricyclic compound LILLY CO ELI (US) 2000-01-05 CN disclosed
EP-0952149-A2 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitiors ELI LILLY AND COMPANY (US) 1999-10-27 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 (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-20050026988-A1 Cyclopenta'b! indole derivatives as spla inhibitors PTGIS, PLA2G4A, PLA2G4B TDP1 2766/4885HDAC1 3437/4885HDAC8 4055/4885
US-20150336891-A1 Zinc Halide Mediated Cyclization Process Leading to Tricyclic Indoles IDO1, IDO2, TPH2 TDP1 3208/4885HDAC1 111/4885HDAC8 451/4885
US-20040198801-A1 Cyclohept'b!indole derivatives as spla2 inhibitors SPTSSB, CPT1A, TPH2 TDP1 2538/4885HDAC1 2499/4885HDAC8 3581/4885

“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.