SCHEMBL1127579

SCHEMBL1127579

c1ccc(C[Se]Cc2ccccc2)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 2/20 0.52
▸ CYP1A1 P04798 1/20 0.52
▸ CYP1B1 Q16678 1/20 0.52
▸ CALM1 P0DP23 1/20 0.50
▸ TSHR P16473 3/20 0.45
▸ ALDH1A1 P00352 2/20 0.45
▸ LOXL2 Q9Y4K0 2/20 0.45
▸ IDO1 P14902 1/20 0.45
▸ TP53 P04637 1/20 0.45
▸ TRPA1 O75762 1/20 0.45
▸ MAOB P27338 1/20 0.43
▸ HPGD P15428 1/20 0.43
▸ ALOX15 P16050 1/20 0.43
▸ ALOX12 P18054 1/20 0.43
▸ CASP1 P29466 1/20 0.43
▸ HSD17B10 Q99714 1/20 0.43
▸ TAAR1 Q96RJ0 2/20 0.42
▸ FAAH O00519 1/20 0.42
▸ PRSS1 P07477 1/20 0.42
▸ PRSS2 P07478 1/20 0.42

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
SCHEMBL3088081 0.97 CYP1A2 (0.50) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL4406066 0.91 CYP1A2 (0.46) CYP1A2CYP1A1CYP1B1CALM1TSHR
Cyanide SCHEMBL21808145 0.91 CYP1A1 (0.52) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL1127627 0.84 FNTA (0.54) CYP1A2IDO1CA1CA2CA9
Bisbenzyldiselenide SCHEMBL441260 0.80 CYP1A1 (0.52) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL28859310 0.79 CYP1A2 (0.41) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL28452710 0.79 TP53 (0.46) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL9279484 0.78 — —
Bisbenzyldiselenide SCHEMBL29169728 0.78 CYP1A1 (0.56) CYP1A2CYP1A1CYP1B1CALM1TSHR
SCHEMBL28439038 0.75 TP53 (0.42) CYP1A2CYP1A1CYP1B1TP53HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114920916-B Continuous synthesis method of poly (butylene succinate) 上海师范大学 2023-11-28 — — CN claimed
CN-113980252-B Continuous production method of modified poly (butylene succinate) 上海师范大学 2023-09-01 — — CN claimed
CN-112501583-B Preparation method of transition metal diselenide film 北京大学深圳研究生院 2023-01-24 — — CN claimed
CN-113980252-A Continuous production method of modified poly (butylene succinate) 上海师范大学 2022-01-28 — — CN claimed
CN-112501583-A Preparation method of transition metal diselenide film 北京大学深圳研究生院 2021-03-16 — — CN claimed
CN-104477856-B A kind of synthetic method of cadmium telluride quantum dot and the synthetic method of II type cadmium telluride core-shell quanta dots CHAO HU UNIVERSITY (CN) 2016-03-09 — — CN claimed
CN-103911155-B A kind of core-shell quanta dots of red-emitting and synthetic method thereof CHAO HU UNIVERSITY (CN) 2016-01-20 — — CN claimed
CN-104477856-A Synthesis method of cadmium telluride quantum dots and synthesis method of Type II cadmium telluride core-shell quantum dots CHAO HU UNIVERSITY 2015-04-01 — — CN claimed
CN-103911155-A Red light-emitting core-shell quantum dot and synthetic method thereof CHAO HU UNIVERSITY 2014-07-09 — — CN claimed
US-6482311-B1 Methods for suppression of filamentous coke formation TDA RESEARCH, INC. 2002-11-19 — — US claimed
US-20020128161-A1 Materials and methods for suppression of filamentous coke formation AIR FORCE, UNITED STATES 2002-09-12 — — US claimed
US-20260132541-A1 SYNTHESIS OF MONOLAYER TRANSITION METAL DICHALCOGENIDES BY ELECTROSTATIC SELF-ASSEMBLY CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2026-05-14 — — US disclosed
US-12379525-B2 Plastic lens DAICEL CORPORATION (JP) 2025-08-05 — — US disclosed
US-20250242575-A1 HARDCOAT-LESS FILM, LAMINATE, MULTILAYER LAMINATE, AND DISPLAY DEVICE DAICEL CORPORATION (JP) 2025-07-31 — — US disclosed
US-20250248279-A1 TRANSPARENT LAMINATE, IMAGE DISPLAY DEVICE, AND FLEXIBLE DEVICE DAICEL CORPORATION (JP) 2025-07-31 — — US disclosed
US-4013528-A SELENOUREA COMPOUND DECOMPOSED TO SELENIUM XEROX CORPORATION (US) 1977-03-22 — — US disclosed
US-4007101-A DECOMPOSITION OF ORGANO-SELENIUM COMPOUNDS XEROX CORPORATION (US) 1977-02-08 — — US disclosed
US-4007100-A Process for preparation of solid phase dispersion of photoconductive materials XEROX CORPORATION (US) 1977-02-08 — — US disclosed
US-3994791-A FORMING SELENIUM FROM ORGANO-SELENIUM COMPOUNDS XEROX CORPORATION (US) 1976-11-30 — — US disclosed
US-3967964-A Photosensitive film comprising an organopolyselenide and an organomercury compound XEROX CORPORATION (US) 1976-07-06 — — 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 (1 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-20260132541-A1 SYNTHESIS OF MONOLAYER TRANSITION METAL DICHALCOGENIDES BY ELECTROSTATIC SELF-ASSEMBLY DCX, DSG1, MEF2D CYP1A2 2428/4885CYP1A1 3215/4885CYP1B1 3203/4885

“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.

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