SCHEMBL198077

SCHEMBL198077

O=C(O)c1c(I)ccnc1F

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 3/20 0.46
KDM4E B2RXH2 6/20 0.44
ASPH Q12797 2/20 0.44
KDM8 Q8N371 2/20 0.44
ALDH1A1 P00352 3/20 0.34
KDM5A P29375 2/20 0.34
KDM3A Q9Y4C1 2/20 0.34
KDM6B O15054 1/20 0.34
TET3 O43151 1/20 0.34
KDM4A O75164 1/20 0.34
BBOX1 O75936 1/20 0.34
MAPT P10636 1/20 0.34
KDM5C P41229 1/20 0.34
KDM4D Q6B0I6 1/20 0.34
TET2 Q6N021 1/20 0.34
ALKBH5 Q6P6C2 1/20 0.34
KDM7A Q6ZMT4 1/20 0.34
TET1 Q8NFU7 1/20 0.34
EGLN2 Q96KS0 1/20 0.34
FTO Q9C0B1 1/20 0.34

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
SCHEMBL31281607 1.00 NAPRT (0.46) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL28280472 0.83 KDM4E (0.38) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL2674661 0.82 NAPRT (0.36) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL15549181 0.82 NAPRT (0.36) NAPRTKDM4EASPHKDM8MAPT
SCHEMBL26618917 0.82 NAPRT (0.36) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL2114463 0.79 NAPRT (0.48) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL3516266 0.78 CA12 (0.40) KDM4EALDH1A1KDM3AKDM6BKDM5C
SCHEMBL29004701 0.78 FFAR1 (0.35) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL30634909 0.78 GAA (0.37) NAPRTKDM4EASPHKDM8ALDH1A1
SCHEMBL26618864 0.78 GAA (0.37) NAPRTKDM4EASPHKDM8ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107328-A1 AGONISTS OF PARATHYROID HORMONE 1 AND INCRETIN RECEPTORS SEPTERNA, INC. (US) 2026-05-21 WO disclosed
US-20250250293-A1 INHIBITORS OF MEK KINASE MOSAICA MEDICINES, INC. 2025-08-07 US disclosed
US-20250214995-A1 CONDENSED BICYCLIC HETEROAROMATIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2025-07-03 US disclosed
WO-2025088571-A1 CRYSTALLINE FORMS OF TEAD INHIBITOR ASTRAZENECA AB (SE) 2025-05-01 WO disclosed
EP-4514793-A1 CONDENSED BICYCLIC HETEROAROMATIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER Astrazeneca AB (SE) 2025-03-05 EP disclosed
EP-4486750-A1 INHIBITORS OF MEK KINASE Kinnate Biopharma Inc. (US) 2025-01-08 EP disclosed
CN-119156385-A Fused bicyclic heteroaromatic compounds and their use in the treatment of cancer 阿斯利康(瑞典)有限公司 2024-12-17 CN disclosed
US-12122800-B2 Inhibitors of MEK kinase KINNATE BIOPHARMA INC. (US) 2024-10-22 US disclosed
US-11976083-B2 Inhibitors of peptidylarginine deiminases GILEAD SCIENCES, INC. (US) 2024-05-07 US disclosed
CN-115551862-B Macrocyclic inhibitors of peptidyl arginine deiminase 吉利德科学公司 2024-04-12 CN disclosed
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE AMGEN INC. (US) 2011-05-19 US disclosed
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE AMGEN INC. (US) 2011-05-19 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US disclosed
EP-1881976-A1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS Amgen Inc., (US) 2008-01-30 EP disclosed
WO-2006116713-A1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS AMGEN INC. (US) 2006-11-02 WO 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 (6 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-12122800-B2 Inhibitors of MEK kinase BRAF, NRAS, RAF1 NAPRT 1960/4885KDM4E 940/4885ASPH 3099/4885
US-11976083-B2 Inhibitors of peptidylarginine deiminases PADI4, PADI2, PADI1 NAPRT 1433/4885KDM4E 936/4885ASPH 1852/4885
US-20080312232-A1 Substituted amide derivatives and methods of use HGF, HGFAC, MET NAPRT 467/4885KDM4E 3651/4885ASPH 29/4885
US-20250250293-A1 INHIBITORS OF MEK KINASE BRAF, NRAS, RAF1 NAPRT 1960/4885KDM4E 940/4885ASPH 3099/4885
US-20250214995-A1 CONDENSED BICYCLIC HETEROAROMATIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, TP53, SDHA NAPRT 2134/4885KDM4E 2306/4885ASPH 1496/4885
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE HGF, HGFAC, MET NAPRT 467/4885KDM4E 3651/4885ASPH 29/4885

“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.