SCHEMBL21243898

SCHEMBL21243898

Cc1c(Cl)cc2c(cnn2C2CCCCO2)c1B1OC(C)(C)C(C)(C)O1

nearest known ligand 0.36

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP4F2 P78329 2/20 0.36
CYP4A11 Q02928 2/20 0.36
RXRA P19793 1/20 0.36
RXRB P28702 1/20 0.36
RXRG P48443 1/20 0.36
DGAT2 Q96PD7 1/20 0.35
ALDH1A1 P00352 1/20 0.33
LMNA P02545 1/20 0.33
POLB P06746 1/20 0.33
RET P07949 1/20 0.32
ATR Q13535 1/20 0.31
PDE1A P54750 2/20 0.31
PDE1B Q01064 2/20 0.31
PDE1C Q14123 2/20 0.31
YTHDC1 Q96MU7 1/20 0.30

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
SCHEMBL29418904 1.00 CYP4F2 (0.36) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL23546535 0.91 RXRA (0.36) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL23043733 0.89 CYP4F2 (0.39) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL25795327 0.88 RXRA (0.40) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL31127775 0.88 RXRA (0.35) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL21379111 0.88 CYP4F2 (0.40) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL21243880 0.88 CYP4F2 (0.38) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL29592576 0.88 CYP4F2 (0.40) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL31527219 0.87 RXRA (0.34) CYP4F2CYP4A11RXRARXRBRXRG
SCHEMBL24802911 0.87 RXRA (0.34) CYP4F2CYP4A11RXRARXRBRXRG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
US-12624033-B2 KRAS inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2026-05-12 US disclosed
US-20250250271-A1 KRAS INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2025-08-07 US disclosed
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-06-12 US disclosed
US-20250154148-A1 KRAS INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2025-05-15 US disclosed
EP-4548918-A2 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS Incyte Corporation (US) 2025-05-07 EP disclosed
US-20250059205-A1 Heterocyclic Compounds and Methods of Use AMGEN INC. (US) 2025-02-20 US disclosed
US-20240409558-A1 IRREVERSIBLE INHIBITORS OF KRAS BIOMEA FUSION, INC. 2024-12-12 US disclosed
US-20240309020-A1 KRAS G12D INHIBITORS ARRAY BIOPHARMA INC. 2024-09-19 US disclosed
US-20240239788-A1 SMALL MOLECULE INHIBITORS OF KRAS G12D MUTANT TAIHO PHARMACEUTICAL CO., LTD. (JP) 2024-07-18 US disclosed
CN-114615981-A KRAS G12D inhibitors 米拉蒂治疗股份有限公司 2022-06-10 CN disclosed
US-20210355121-A1 FUSED TRICYCLIC KRAS INHIBITORS INCYTE CORPORATION 2021-11-18 US disclosed
WO-2021211864-A1 FUSED TRICYCLIC KRAS INHIBITORS INCYTE CORPORATION (US) 2021-10-21 WO disclosed
WO-2021041671-A1 KRAS G12D INHIBITORS Mirati Therapeutics, Inc. (US) 2021-03-04 WO disclosed
EP-3749665-A1 TETRAHYDROQUINAZOLINE DERIVATIVES USEFUL AS ANTICANCER AGENTS Pfizer Inc. (US) 2020-12-16 EP disclosed
US-20200331911-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. 2020-10-22 US disclosed
US-20200331911-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. 2020-10-22 US disclosed
US-10590115-B2 Tetrahydroquinazoline derivatives useful as anticancer agents PFIZER INC. (US) 2020-03-17 US disclosed
US-20190248767-A1 Tetrahydroquinazoline Derivatives Useful as Anticancer Agents PFIZER INC. (US) 2019-08-15 US disclosed
WO-2019155399-A1 TETRAHYDROQUINAZOLINE DERIVATIVES USEFUL AS ANTICANCER AGENTS PFIZER INC. (US) 2019-08-15 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 (13 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-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS CYP4F2 3406/4885CYP4A11 1064/4885RXRA 4205/4885
US-20190248767-A1 Tetrahydroquinazoline Derivatives Useful as Anticancer Agents TOP2A, TOP1, TOP2B CYP4F2 579/4885CYP4A11 1687/4885RXRA 4159/4885
US-20240409558-A1 IRREVERSIBLE INHIBITORS OF KRAS KRAS, NRAS, TP53 CYP4F2 4657/4885CYP4A11 4349/4885RXRA 2045/4885
US-10590115-B2 Tetrahydroquinazoline derivatives useful as anticancer agents TOP2A, TOP1, TOP2B CYP4F2 579/4885CYP4A11 1687/4885RXRA 4159/4885
US-20250059205-A1 Heterocyclic Compounds and Methods of Use KRAS, NRAS, HRAS CYP4F2 2561/4885CYP4A11 1528/4885RXRA 2831/4885
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS CYP4F2 2828/4885CYP4A11 2524/4885RXRA 3260/4885
US-20240239788-A1 SMALL MOLECULE INHIBITORS OF KRAS G12D MUTANT KRAS, NRAS, HRAS CYP4F2 4690/4885CYP4A11 4627/4885RXRA 3326/4885
US-20250154148-A1 KRAS INHIBITORS KRAS, NRAS, HRAS CYP4F2 4675/4885CYP4A11 4085/4885RXRA 3532/4885
US-20250250271-A1 KRAS INHIBITORS KRAS, NRAS, HRAS CYP4F2 4675/4885CYP4A11 4085/4885RXRA 3532/4885
US-20200331911-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS CYP4F2 4223/4885CYP4A11 1434/4885RXRA 3298/4885
US-20210355121-A1 FUSED TRICYCLIC KRAS INHIBITORS KRAS, NRAS, HRAS CYP4F2 2545/4885CYP4A11 2241/4885RXRA 3493/4885
US-12624033-B2 KRAS inhibitors KRAS, NRAS, BRAF CYP4F2 4423/4885CYP4A11 3994/4885RXRA 4744/4885
US-20240309020-A1 KRAS G12D INHIBITORS KRAS, NRAS, HRAS CYP4F2 3182/4885CYP4A11 991/4885RXRA 3173/4885

“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.