SCHEMBL29431119

SCHEMBL29431119

COc1ccc(-c2c3nc(c(-c4ccc(OC)cc4)c4ccc([nH]4)c(-c4ccc(OC)cc4)c4nc(c(-c5ccc(OC)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1.[Co+2]

nearest known ligand 0.55

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ TERT O14746 4/20 0.55
▸ ABCG2 Q9UNQ0 1/20 0.55
▸ TOP1 P11387 4/20 0.54
▸ CYCS P99999 4/20 0.53
▸ ENPP2 Q13822 1/20 0.51
▸ KDM4E B2RXH2 2/20 0.44
▸ NPC1 O15118 2/20 0.44
▸ RAB9A P51151 2/20 0.44
▸ MAPT P10636 1/20 0.44
▸ CASP3 P42574 1/20 0.44
▸ SENP8 Q96LD8 1/20 0.44
▸ SENP7 Q9BQF6 1/20 0.44
▸ SENP6 Q9GZR1 1/20 0.44
▸ ALDH1A1 P00352 1/20 0.43
▸ PKM P14618 1/20 0.43
▸ SMN1; SMN2 Q16637 1/20 0.43

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
SCHEMBL30539978 1.00 TERT (0.55) TERTABCG2TOP1CYCSENPP2
Hydrochloric Acid SCHEMBL31122235 0.98 TERT (0.54) TERTABCG2TOP1CYCSENPP2
SCHEMBL29414382 0.98 TERT (0.57) TERTABCG2TOP1CYCSENPP2
SCHEMBL949511 0.98 TERT (0.57) TERTABCG2TOP1CYCSENPP2
SCHEMBL2338257 0.97 TERT (0.55) TERTABCG2TOP1CYCSENPP2
SCHEMBL22265228 0.97 TERT (0.55) TERTABCG2TOP1CYCSENPP2
SCHEMBL20856304 0.97 TERT (0.59) TERTABCG2TOP1CYCSENPP2
SCHEMBL8430292 0.97 TERT (0.55) TERTABCG2TOP1CYCSENPP2
Hydrochloric Acid SCHEMBL15768782 0.97 TERT (0.55) TERTABCG2TOP1CYCSENPP2
SCHEMBL29515314 0.97 TERT (0.55) TERTABCG2TOP1CYCSENPP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250270352-A1 METHODS OF REVERSIBLE-ADDITION FRAGMENTATION CHAIN TRANSFER STEP-GROWTH POLYMERIZATION AND POLYMERS THEREFROM NATIONAL SCIENCE FOUNDATION 2025-08-28 — — US disclosed
CN-119360107-A Silage quality detection method and silage quality detection system 内蒙古农业大学 2025-01-24 — — CN disclosed
EP-3965928-B1 PROCESS FOR PREPARING POLYPROPYLENE CARBONATE ENI SPA (IT) 2024-07-03 — — EP disclosed
CN-118176223-A Process for reversible-addition fragmentation chain transfer step-growth polymerization and polymers prepared by the same 北卡罗来纳大学教堂山分校 2024-06-11 — — CN disclosed
EP-2602655-B1 Ophthalmic filter ESSILOR INT (FR) 2024-04-03 — — EP disclosed
CN-117783019-A On-site detection method of CTC black tea production place based on solution phase color sensing array 安徽农业大学 2024-03-29 — — CN disclosed
US-11865521-B2 Bifunctional catalyst for hydrogenation of carbon dioxide, and method for preparing hydrocarbon by using same KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2024-01-09 — — US disclosed
US-11753551-B2 Stable organic light emitting coating YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. 2023-09-12 — — US disclosed
US-11733203-B2 Sensing cell and sensing device NATIONAL TSING HUA UNIVERSITY (TW) 2023-08-22 — — US disclosed
US-11635547-B2 Composition for the manufacture of an ophthalmic lens comprising an encapsulated light-absorbing additive ESSILOR INTERNATIONAL (FR) 2023-04-25 — — US disclosed
EP-2602654-B1 Ophthalmic filter ESSILOR INT (FR) 2023-04-19 — — EP disclosed
EP-3497488-B2 OPHTALMIC LENS COMPRISING AN ENCAPSULATED LIGHT-ABSORBING ADDITIVE ESSILOR INT (FR) 2023-03-22 — — EP disclosed
WO-2023034335-A1 METHODS OF REVERSIBLE-ADDITION FRAGMENTATION CHAIN TRANSFER STEP-GROWTH POLYMERIZATION AND POLYMERS THEREFROM THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2023-03-09 — — WO disclosed
CN-113571719-B Biomass carbon material derived transition metal-based catalyst, preparation method and application thereof, and solid zinc-air battery 云南大学 2022-09-30 — — CN disclosed
CN-109564297-B Ophthalmic lenses comprising encapsulated light absorbing additives 依视路国际公司 2022-08-16 — — CN disclosed
US-20220220253-A1 PROCESS FOR PREPARING POLYPROPYLENE CARBONATE ENI S.P.A. (IT) 2022-07-14 — — US disclosed
US-11327202-B2 Composition for the manufacture of an ophthalmic lens comprising an encapsulated light-absorbing additive ESSILOR INTERNATIONAL (FR) 2022-05-10 — — US disclosed
US-20220128508-A1 SENSING CELL AND SENSING DEVICE NATIONAL TSING HUA UNIVERSITY (TW) 2022-04-28 — — US disclosed
US-20220088578-A1 BIFUNCTIONAL CATALYST FOR HYDROGENATION OF CARBON DIOXIDE, AND METHOD FOR PREPARING HYDROCARBON BY USING SAME KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2022-03-24 — — US disclosed
EP-3965928-A1 PROCESS FOR PREPARING POLYPROPYLENE CARBONATE ENI S.p.A. (IT) 2022-03-16 — — 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-20220088578-A1 BIFUNCTIONAL CATALYST FOR HYDROGENATION OF CARBON DIOXIDE, AND METHOD FOR PREPARING HYDROCARBON BY USING SAME TDO2, SCO2, HAO2 TERT 58/4885ABCG2 4720/4885TOP1 352/4885
US-11865521-B2 Bifunctional catalyst for hydrogenation of carbon dioxide, and method for preparing hydrocarbon by using same TDO2, SCO2, HAO2 TERT 58/4885ABCG2 4720/4885TOP1 352/4885
US-20220220253-A1 PROCESS FOR PREPARING POLYPROPYLENE CARBONATE PPOX, PGM2, POLR2B TERT 610/4885ABCG2 4445/4885TOP1 904/4885

“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.

Send feedback