SCHEMBL737479

SCHEMBL737479

OCc1cc(Cl)c(O)c(Cl)c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 6/20 0.52
TSHR P16473 5/20 0.52
CYP3A4 P08684 3/20 0.52
RECQL P46063 3/20 0.52
TTR P02766 2/20 0.52
ALDH1A1 P00352 1/20 0.52
ACHE P22303 2/20 0.50
THRB P10828 2/20 0.48
CYP2C9 P11712 3/20 0.46
CYP1A2 P05177 3/20 0.46
CYP2C19 P33261 3/20 0.46
ALOX15 P16050 2/20 0.46
ALOX12 P18054 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
HIF1A Q16665 2/20 0.46
KDM4E B2RXH2 1/20 0.43
CASP6 P55212 1/20 0.43
CYP2D6 P10635 2/20 0.42
HPGD P15428 3/20 0.42
MAPK1 P28482 2/20 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
Phosphonic Acid SCHEMBL4093450 0.89 HSD17B10 (0.42) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL13365218 0.87 ACHE (0.44) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL9812457 0.85 KDM4E (0.57) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL3913401 0.83 ERN1 (0.41) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL4093452 0.82 TSHR (0.37) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL1965439 0.80 HPGD (0.48) HSD17B10TSHRCYP3A4RECQLALDH1A1
SCHEMBL70208 0.80 HSD17B10 (0.55) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL7885118 0.80 HSD17B10 (0.55) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL2927011 0.79 HSD17B10 (0.48) HSD17B10TSHRCYP3A4RECQLTTR
SCHEMBL4825263 0.79 TRPV1 (0.49) HSD17B10TSHRTHRBALOX15KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12577236-B2 Processes for preparation of Tezacaftor LAURUS LABS LIMITED (IN) 2026-03-17 US disclosed
CN-119913563-A PtZn-ZnOx interface active site-rich catalyst for low-potential benzoic acid production, and preparation method and application thereof 华南理工大学 2025-05-02 CN disclosed
US-20250044700-A1 PATTERN FORMING METHOD AND METHOD FOR PRODUCING ELECTRONIC DEVICE FUJIFILM CORPORATION (JP) 2025-02-06 US disclosed
WO-2024254923-A1 POLYMER FOR PHOTOETCHING MEDIUM COMPOSITION, AND PHOTOETCHING MEDIUM COMPOSITION 嘉庚创新实验室 2024-12-19 WO disclosed
CN-115975561-B E (E)NFPreparation method of graded lignan-based wood adhesive 中国林业科学研究院林产化学工业研究所 2024-12-17 CN disclosed
EP-4405097-B1 VPO CATALYST HAVING IMPROVED SELECTIVITY AND STABILITY AND METHOD FOR THE PREPARATION THEREOF CLARIANT INT LTD (CH) 2024-11-20 EP disclosed
CN-118957652-A Nickel-based bimetallic phosphide catalyst and preparation method and application thereof 中国地质大学(武汉) 2024-11-15 CN disclosed
CN-118420442-B Method for preparing vanillin by reducing vanillin with silicon powder 天津市职业大学 2024-09-13 CN disclosed
CN-118420442-A Method for preparing vanillin by reducing vanillin with silicon powder 天津市职业大学 2024-08-02 CN disclosed
EP-4405097-A1 VPO CATALYST HAVING IMPROVED SELECTIVITY AND STABILITY AND METHOD FOR THE PREPARATION THEREOF Clariant International Ltd (CH) 2024-07-31 EP disclosed
US-5183810-A Hyptoensive agents MERCK & CO., INC. (US) 1993-02-02 US disclosed
EP-0517812-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO. INC. (US) 1992-12-16 EP disclosed
EP-0515548-A1 IMIDAZOLE ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO. INC. (US) 1992-12-02 EP disclosed
EP-0515535-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO. INC. (US) 1992-12-02 EP disclosed
WO-1991011999-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO., INC. (US) 1991-08-22 WO disclosed
WO-1991012001-A1 ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO., INC. (US) 1991-08-22 WO disclosed
WO-1991012002-A1 IMIDAZOLE ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED BENZYL ELEMENT MERCK & CO., INC. (US) 1991-08-22 WO disclosed
US-4923885-A PSORIASIS, GASTROINTESTINAL DISORDERS, SKIN DISORDERS; ANTICARCINOGENIC, ANTITUMOR, AND ANTIGROWTH AGENTS MERCK & CO., INC. (US) 1990-05-08 US disclosed
US-4525304-A Process for preparing oxazolinoazetidinones ELI LILLY AND COMPANY (US) 1985-06-25 US disclosed
EP-0109817-A2 Process for preparing oxazolinoazetidinones ELI LILLY AND COMPANY (US) 1984-05-30 EP 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-12577236-B2 Processes for preparation of Tezacaftor CYP4A11, F9, CYP3A4 HSD17B10 912/4885TSHR 34/4885CYP3A4 3/4885

“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.