SCHEMBL263386

SCHEMBL263386

CC1(C)OB(c2ccccc2OC(F)F)OC1(C)C

nearest known ligand 0.39

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ LPL P06858 3/20 0.39
▸ LIPG Q9Y5X9 3/20 0.39
▸ TNF P01375 1/20 0.37
▸ KMT2A Q03164 1/20 0.35
▸ LIPE Q05469 6/20 0.34
▸ HTT P42858 1/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.34
▸ ALOX12 P18054 1/20 0.34
▸ NR1I2 O75469 1/20 0.33
▸ DRD1 P21728 1/20 0.33
▸ BACE1 P56817 1/20 0.33
▸ CXCR2 P25025 2/20 0.33

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
SCHEMBL29574549 1.00 LPL (0.39) LPLLIPGTNFKMT2ALIPE
SCHEMBL4315605 0.91 KMT2A (0.35) LPLLIPGTNFKMT2ALIPE
SCHEMBL2026497 0.86 LPL (0.38) LPLLIPGTNFKMT2ALIPE
SCHEMBL31648336 0.86 JAK2 (0.38) LPLLIPGTNFLIPENR1I2
SCHEMBL26197525 0.83 LPL (0.33) LPLLIPGTNFBACE1
SCHEMBL13727784 0.83 LPL (0.41) LPLLIPGTNFCXCR2
SCHEMBL29878543 0.83 LPL (0.41) LPLLIPGTNFCXCR2
SCHEMBL14358557 0.83 LPL (0.41) LPLLIPGTNFKMT2ALIPE
SCHEMBL22131084 0.80 LPL (0.44) LPLLIPGLIPE
SCHEMBL25367719 0.80 MEN1 (0.36) LPLLIPGKMT2ALIPESMN1; SMN2

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 69 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-20260049074-A1 THIADIAZOLYL DERIVATIVES IDEAYA BIOSCIENCES, INC. (US) 2026-02-19 — — US disclosed
US-20260015360-A1 BIARYL DERIVATIVES AND RELATED USES MOMA THERAPEUTICS, INC. 2026-01-15 — — US disclosed
US-12509454-B2 Thiadiazolyl derivatives IDEAYA BIOSCIENCES, INC. (US) 2025-12-30 — — US disclosed
US-12187684-B2 Benzimidazole derivatives as modulators of retinoid-related orphan receptor gamma (RORγ) and pharmaceutical use thereof JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2025-01-07 — — US disclosed
US-20240309020-A1 KRAS G12D INHIBITORS ARRAY BIOPHARMA INC. 2024-09-19 — — US disclosed
US-11964989-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2024-04-23 — — US disclosed
CN-114615981-B KRAS G12D inhibitors 米拉蒂治疗股份有限公司 2024-04-12 — — CN disclosed
CN-114502535-B Acid addition salts of rory modulators 江苏恒瑞医药股份有限公司 2024-04-12 — — CN disclosed
US-20240059689-A1 PURINE DERIVATIVES AS ANTICANCER AGENTS MEDIVIR AB (SE) 2024-02-22 — — US disclosed
US-20090048306-A1 PYRIDINE DERIVATIVES PFIZER, INC. (US) 2009-02-19 — — US disclosed
US-20090048306-A1 PYRIDINE DERIVATIVES PFIZER, INC. (US) 2009-02-19 — — US disclosed
US-20090048306-A1 PYRIDINE DERIVATIVES PFIZER, INC. (US) 2009-02-19 — — US disclosed
WO-2008135826-A2 2 -PYRIDINE CARBOXAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS PFIZER LIMITED (GB) 2008-11-13 — — WO disclosed
WO-2008135826-A2 2 -PYRIDINE CARBOXAMIDE DERIVATIVES AS SODIUM CHANNEL MODULATORS PFIZER LIMITED (GB) 2008-11-13 — — WO disclosed
WO-2008124850-A1 FUSED RING HETEROCYCLE KINASE MODULATORS SGX PHARMACEUTICALS, INC. (US) 2008-10-16 — — WO disclosed
WO-2008124850-A1 FUSED RING HETEROCYCLE KINASE MODULATORS SGX PHARMACEUTICALS, INC. (US) 2008-10-16 — — WO disclosed
US-20070287711-A1 FUSED RING HETEROCYCLE KINASE MODULATORS SGX PHARMACEUTICALS, INC. (US) 2007-12-13 — — US disclosed
US-20070287711-A1 FUSED RING HETEROCYCLE KINASE MODULATORS SGX PHARMACEUTICALS, INC. (US) 2007-12-13 — — US disclosed
US-20070287711-A1 FUSED RING HETEROCYCLE KINASE MODULATORS SGX PHARMACEUTICALS, INC. (US) 2007-12-13 — — 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 (10 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-20240059689-A1 PURINE DERIVATIVES AS ANTICANCER AGENTS RRM2, TYMP, PNP LPL 4447/4885LIPG 4853/4885TNF 2662/4885
US-20260049074-A1 THIADIAZOLYL DERIVATIVES POLH, POLM, POLD1 LPL 2017/4885LIPG 1727/4885TNF 4669/4885
US-20260015360-A1 BIARYL DERIVATIVES AND RELATED USES POLB, POLA1, POLN LPL 1951/4885LIPG 1995/4885TNF 4786/4885
US-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS LPL 3982/4885LIPG 2426/4885TNF 4086/4885
US-20070287711-A1 FUSED RING HETEROCYCLE KINASE MODULATORS MAP3K20, TTK, MAP3K19 LPL 4301/4885LIPG 2925/4885TNF 4407/4885
US-20090048306-A1 PYRIDINE DERIVATIVES SDHA, P2RX4, P2RX3 LPL 3931/4885LIPG 4769/4885TNF 959/4885
US-12187684-B2 Benzimidazole derivatives as modulators of retinoid-related orphan receptor gamma (RORγ) and pharmaceutical use thereof RORC, RORB, RORA LPL 2423/4885LIPG 3577/4885TNF 2626/4885
US-11964989-B2 KRas G12D inhibitors KRAS, NRAS, HRAS LPL 3923/4885LIPG 3144/4885TNF 4230/4885
US-12509454-B2 Thiadiazolyl derivatives POLD1, POLQ, DNA2 LPL 1462/4885LIPG 2091/4885TNF 3415/4885
US-20240309020-A1 KRAS G12D INHIBITORS KRAS, NRAS, HRAS LPL 4181/4885LIPG 3541/4885TNF 3636/4885

“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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