Tegafur

Tegafur

SCHEMBL4552

O=c1[nH]c(=O)n(C2CCCO2)cc1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TYMS

The experimentally established mechanism targets of Tegafur. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 1.00
MAPT P10636 2/20 1.00
ESR1 P03372 1/20 1.00
SMN1; SMN2 Q16637 3/20 0.69
ALDH1A1 P00352 2/20 0.69
KMT2A Q03164 2/20 0.69
POLB P06746 1/20 0.69
HPGD P15428 1/20 0.45
TSHR P16473 1/20 0.45
PMP22 Q01453 1/20 0.45
HBB P68871 1/20 0.45
HDAC1 Q13547 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
MEN1 O00255 1/20 0.38

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
Tegafur SCHEMBL8537231 1.00 LMNA (1.00) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL7698456 1.00 LMNA (1.00) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL4553 1.00 LMNA (1.00) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL4155129 0.98 LMNA (0.97) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL22320166 0.98 LMNA (0.97) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL28304686 0.97 LMNA (0.94) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL28156468 0.97 LMNA (0.94) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL28851751 0.96 LMNA (0.92) LMNAMAPTESR1SMN1; SMN2ALDH1A1
SCHEMBL10940658 0.95 LMNA (0.91) LMNAMAPTESR1SMN1; SMN2ALDH1A1
Tegafur SCHEMBL1276356 0.90 LMNA (0.81) LMNAMAPTESR1SMN1; SMN2ALDH1A1

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

Appears in 55523 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260141690-A1 LAYER-WISE KNOWLEDGE DISTILLATION FOR VISION LANGUAGE MODELS NVIDIA CORP (US) 2026-05-21 US claimed
CN-122056884-A Methods of treating pancreatic cancer 坎莫森特里克斯公司 2026-05-19 CN claimed
CN-122028934-A Combination of CLDN18_2 antibody and chemotherapeutic drug and application thereof 江苏奥赛康生物医药有限公司 2026-05-12 CN claimed
CN-122011207-A CAR-T cell over-expressing H2A.Z as well as preparation method and application thereof 中国科学院微生物研究所 2026-05-12 CN claimed
CN-122006800-A Cu@TS-1 molecular sieve catalyst and preparation method and application thereof 石河子大学 2026-05-12 CN claimed
EP-3978473-B1 COMPOUND CONTAINING AN INDOLEACETIC ACID CORE STRUCTURE AND USE THEREOF BEIJING AN JIAN XI BIO MEDICAL TECH CO LTD (CN) 2026-05-06 EP claimed
US-20260116861-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-04-30 US claimed
EP-4729063-A2 TREATMENT OF CANCER USING COENZYME Q10 COMBINATION THERAPIES BPGbio, Inc. (US) 2026-04-22 EP claimed
EP-3515892-B1 COMPOUNDS AND METHODS FOR IDO AND TDO MODULATION, AND INDICATIONS THEREFOR PLEXXIKON INC (US) 2026-04-15 EP claimed
EP-4720132-A1 COMBINATION THERAPIES INVOLVING CLAUDIN 18.2 ANTAGONISTS FOR TREATMENT OF CANCER Suzhou Transcenta Therapeutics Co., Ltd. (CN) 2026-04-08 EP claimed
EP-0227593-A1 Use of chelating agents THE HOSPITAL FOR SICK CHILDREN (CA) 1987-07-01 EP claimed
EP-0224885-A1 Antitumor composition. WAKUNAGA SEIYAKU KABUSHIKI KAISHA (JP) 1987-06-10 EP claimed
US-4650801-A CYTOSINE TO INHIBIT DECOMPOSITION TAIHO PHARMACEUTICAL COMPANY, LTD. (JP) 1987-03-17 US claimed
EP-0180188-A2 A composition for increasing the anti-cancer activity of an anti-cancer compound OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1986-05-07 EP claimed
US-4507301-A Anti-cancer composition for delivering 5-fluorouracil TAIHO PHARMACEUTICAL COMPANY, LIMITED (JP) 1985-03-26 US claimed
US-4328229-A Anti-cancer composition for delivering 5-fluorouracil to cancer tissues TAIHO PHARMACEUTICAL COMPANY LIMITED (JP) 1982-05-04 US claimed
US-4256885-A 5-FLUOROURACIL AND 2,3-DIHYDROFURAN, ACID CATALYSTS MITSUI TOATSU KAGAKU KABUSHIKI KAISHA (JP) 1981-03-17 US claimed
US-4249006-A Method of producing 5-fluorouracil derivatives TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1981-02-03 US claimed
US-3960864-A Method of synthesizing 1-(tetrahydro-2-furanyl)-5-fluorouracil THE UNIVERSITY OF UTAH (US) 1976-06-01 US claimed
US-3948897-A Synthesis of 1-(tetrahydro-2-furanyl)-5-fluorouracil (Ftorafur) via direct fluorination THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF HEALTH, EDUCATION AND WELFARE (US) 1976-04-06 US claimed