SCHEMBL537975

SCHEMBL537975

CC(C)(C)[Si](OS(=O)(=O)C(F)(F)F)(c1ccccc1)c1ccccc1

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.33
PTGS1 P23219 5/20 0.33
PTGS2 P35354 5/20 0.33
HSD11B1 P28845 1/20 0.33
CA1 P00915 1/20 0.32
CA5A P35218 1/20 0.32
CA9 Q16790 1/20 0.32
NR1H2 P55055 2/20 0.32
NR1H3 Q13133 2/20 0.32
SLC22A12 Q96S37 2/20 0.31
ELANE P08246 1/20 0.31
NR1I2 O75469 1/20 0.31
RORA P35398 1/20 0.31
RORC P51449 1/20 0.31
RORB Q92753 1/20 0.31
NR1H4 Q96RI1 1/20 0.31
CHRM1 P11229 1/20 0.30
DRD2 P14416 1/20 0.30
DRD4 P21917 1/20 0.30
DRD3 P35462 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
SCHEMBL17456530 0.84 ELANE (0.39) HSD11B1ELANENR1I2RORARORC
SCHEMBL537825 0.81 NR3C2 (0.33) PTGS1PTGS2HSD11B1
SCHEMBL17839065 0.79 CA2 (0.33) CA2CA1
SCHEMBL17466333 0.79 HTR6 (0.33) SLC22A12
SCHEMBL196247 0.78 NR1H2 (0.37) CA2PTGS1PTGS2HSD11B1CA1
SCHEMBL196180 0.78 NR1H2 (0.37) CA2PTGS1PTGS2HSD11B1CA1
SCHEMBL12501660 0.78 CA2 (0.38) CA2CA1
SCHEMBL537935 0.77 CA2 (0.36) CA2PTGS1PTGS2CA1CA5A
SCHEMBL17839117 0.76 CA2 (0.33) CA2CA1
SCHEMBL3857896 0.76 CA2 (0.35) CA2HSD11B1CA1NR1I2RORA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4673424-A1 LIQUID PHASE PEPTIDE SUPPORT SYNTHESIS OF PEPTIDES AND PEPTIDOMIMETICS Regeneron Pharmaceuticals, Inc. (US) 2026-01-07 EP claimed
US-12331072-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-06-17 US claimed
WO-2025104679-A1 PROCESSES FOR MAKING INTERMEDIATES FOR ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2025-05-22 WO claimed
WO-2025083736-A1 NOVEL PROCESS FOR THE PREPARATION OF PIRTOBRUTINIB AND ITS INTERMEDIATES THEREOF MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2025-04-24 WO claimed
CN-119253064-A Multifunctional electrolyte and lithium metal battery 江苏师范大学 2025-01-03 CN claimed
CN-113056475-B Deprotection method for peptide compound or amide compound and resin removal method in solid phase reaction and method for producing peptide compound 中外制药株式会社 2024-09-24 CN claimed
WO-2024182268-A1 LIQUID PHASE PEPTIDE SUPPORT SYNTHESIS OF PEPTIDES AND PEPTIDOMIMETICS REGENERON PHARMACEUTICALS, INC. (US) 2024-09-06 WO claimed
CN-117683064-A Preparation method of series of fluoro-calcitol CD ring related impurities 正大制药(青岛)有限公司 2024-03-12 CN claimed
CN-117567300-A Synthesis method of gamma-amino alcohol containing continuous chiral center 江苏大学 2024-02-20 CN claimed
CN-117088798-A Preparation method of fluoro-calcitol 22, 23-double bond impurity 正大制药(青岛)有限公司 2023-11-21 CN claimed
CN-114276284-A Preparation method of fluocalcitol 正大制药(青岛)有限公司 2022-04-05 CN claimed
CN-113603631-A Synthesis method of N-benzyl-3-hydroxypiperidine 山东盛安贝新能源有限公司 2021-11-05 CN claimed
CN-113264972-A Method for preparing obeticholic acid 四川科伦药物研究院有限公司 2021-08-17 CN claimed
CN-111286021-A Polyether terminated by silyl ether, preparation method thereof and efficient anti-mud water reducer 安徽海螺新材料科技有限公司 2020-06-16 CN claimed
CN-108165303-B Crude oil demulsifier and preparation method and use method thereof 广昌达新材料技术服务(深圳)股份有限公司 2020-04-17 CN claimed
US-20090286996-A1 PROCESS FOR THE PREPARATION OF ZILEUTON DIPHARMA FRANCIS S.R.I. (IT) 2009-11-19 US claimed
EP-0736052-B1 PROCESS TO REACT EPOXIDE-CONTAINING COMPOUNDS AND ALIPHATIC ALCOHOLS DOW CHEMICAL CO (US) 1999-08-11 EP claimed
US-5728796-A Process to react epoxide-containing compounds and aliphatic alcohols THE DOW CHEMICAL COMPANY (US) 1998-03-17 US claimed
US-4772683-A SILYLATION, AZETIDONE THIOLESTERS BRISTOL-MYERS COMPANY (US) 1988-09-20 US claimed
US-4639335-A ANHYDROPENICILLIN INTERMEDIATE BRISTOL-MYERS COMPANY (US) 1987-01-27 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-12331072-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound VIP, PEPD, MLN CA2 3250/4885PTGS1 2748/4885PTGS2 3176/4885
US-20090286996-A1 PROCESS FOR THE PREPARATION OF ZILEUTON MPO, ZYX, F7 CA2 967/4885PTGS1 2444/4885PTGS2 2559/4885

“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.