SCHEMBL29366152

SCHEMBL29366152

[Ir].c1ccc(-c2ccccn2)cc1.c1ccc(-c2ccccn2)cc1.c1ccc(-c2ccccn2)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 6/20 0.65
LMNA P02545 5/20 0.65
CCR1 P32246 2/20 0.65
CCR5 P51681 2/20 0.65
CCR8 P51685 2/20 0.65
CYP1A2 P05177 2/20 0.65
POLB P06746 1/20 0.65
METAP1 P53582 1/20 0.65
BLM P54132 1/20 0.65
HIF1A Q16665 1/20 0.65
DOHH Q9BU89 1/20 0.65
P4HTM Q9NXG6 1/20 0.65
CYP2A6 P11509 1/20 0.61
RAB9A P51151 8/20 0.54
NPC1 O15118 6/20 0.54
TP53 P04637 5/20 0.54
SMN1; SMN2 Q16637 5/20 0.54
L3MBTL1 Q9Y468 3/20 0.54
PKM P14618 3/20 0.54
TDP1 Q9NUW8 2/20 0.54

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
SCHEMBL354271 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL301762 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL29461566 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL3985205 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL51343 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL30041479 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL6831244 1.00 KDM4E (0.65) KDM4ELMNACCR1CCR5CCR8
SCHEMBL35754 0.97 KDM4E (0.68) KDM4ELMNACCR1CCR5CCR8
Benzene SCHEMBL29224585 0.97 KDM4E (0.68) KDM4ELMNACCR1CCR5CCR8
SCHEMBL29360780 0.97 KDM4E (0.68) KDM4ELMNACCR1CCR5CCR8

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 1268 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119118900-B Method for synthesizing 3-fluorooxindole compound by visible light catalysis NANJING TECH UNIVERSITY (CN) 2026-05-26 CN claimed
CN-117682986-B Synthesis method of beta-pyridone derivative NANCHANG HANGKONG UNIVERSITY (CN) 2026-05-26 CN claimed
CN-122059918-A Synthesis method and application of cyclobutane chroman skeleton molecular compound 昆明理工大学 2026-05-19 CN claimed
CN-122010869-A Dioxygen di-oxygen benzothiazepines Synthesis method of heptanone derivative 新疆大学 2026-05-12 CN claimed
US-20250353825-A1 CANNABICYCLOL DERIVATIVES AND PREPARATION METHODS THEREOF KUNMING UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) 2025-11-20 US claimed
US-12435027-B1 Preparation method of N-butenyl amide compounds ZHEJIANG NORMAL UNIVERSITY (CN) 2025-10-07 US claimed
CN-117776988-B Preparation of gamma, delta-unsaturated ketone compound by visible light-induced free radical reaction 浙江师范大学 2025-06-24 CN claimed
CN-120058635-A Diastereoselective synthesis method and application of polysubstituted cyclobutane 华东理工大学 2025-05-30 CN claimed
CN-120040461-A Spirobarbitudes compound, preparation method and application 北京工业大学 2025-05-27 CN claimed
CN-120040462-A Spiropyrazinone compound, preparation method and application 北京工业大学 2025-05-27 CN claimed
CN-114751919-A Cyclobutane fused spiro indoline compound as well as preparation method and application thereof 华南理工大学 2022-07-15 CN claimed
CN-114736181-A Synthesis method of visible light mediated acylated benzofuran derivative 河南大学 2022-07-12 CN claimed
CN-114539039-A Method for synthesizing chiral fluorophenethyl alcohol by photo-enzyme catalysis 广东省科学院微生物研究所(广东省微生物分析检测中心) 2022-05-27 CN claimed
CN-114478380-A Photo-oxidation-reduction catalysis N-arylamine and cyclic ketoxime ester C (sp)3)-C(sp3) Cross-coupling method 南昌航空大学 2022-05-13 CN claimed
CN-114478388-A Multifunctional pyrazolone compound and preparation method thereof 北京工业大学 2022-05-13 CN claimed
CN-114436882-A Method for synthesizing asymmetric oxamide derivative 浙江工业大学 2022-05-06 CN claimed
CN-114203943-A Preparation method of PDMS (polydimethylsiloxane) in-situ corrugated antireflection film and preparation method of monochromatic organic light emitting diode 上海大学 2022-03-18 CN claimed
CN-114203944-A In-situ porous antireflection film and preparation method of organic light-emitting diode 上海大学 2022-03-18 CN claimed
EP-3966820-A1 LIGHT-ACTIVATED CONTROLLED RADICAL POLYMERIZATION Facebook Technologies, LLC. (US) 2022-03-16 EP claimed
CN-110256211-B Preparation method of 1, 1-diaryl alkane derivative 南昌航空大学 2022-02-25 CN claimed

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-20250353825-A1 CANNABICYCLOL DERIVATIVES AND PREPARATION METHODS THEREOF CNR2, HMOX1, CASP6 KDM4E 880/4885LMNA 806/4885CCR1 3513/4885
US-12435027-B1 Preparation method of N-butenyl amide compounds BBOX1, NAT1, AADAC KDM4E 1745/4885LMNA 599/4885CCR1 4799/4885

“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.