SCHEMBL400254

SCHEMBL400254

CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2c-1nc1ccccc1c2CO

nearest known ligand 0.84

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TOP1 P11387 18/20 0.84
MEN1 O00255 3/20 0.72
KMT2A Q03164 3/20 0.72
ALDH1A1 P00352 3/20 0.69
GLA P06280 3/20 0.69
KDM4E B2RXH2 2/20 0.69
TP53 P04637 2/20 0.69
HPGD P15428 2/20 0.69
SMN1; SMN2 Q16637 2/20 0.69
STAT6 P42226 1/20 0.69
CHEK1 O14757 1/20 0.69
HDAC3 O15379 1/20 0.69
ABCC4 O15439 1/20 0.69
GMNN O75496 1/20 0.69
LMNA P02545 1/20 0.69
CYP1A2 P05177 1/20 0.69
CYP3A4 P08684 1/20 0.69
HNRNPA1 P09651 1/20 0.69
GAA P10253 1/20 0.69
ALOX15 P16050 1/20 0.69

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
SCHEMBL10130707 1.00 TOP1 (0.84) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL30902657 1.00 TOP1 (0.84) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL29363060 0.94 TOP1 (0.85) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL1005149 0.94 TOP1 (0.85) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL19236135 0.94 TOP1 (0.85) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL29649464 0.94 TOP1 (0.85) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL27606708 0.93 TOP1 (0.86) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL11070279 0.93 TOP1 (0.86) TOP1MEN1KMT2AALDH1A1GLA
SCHEMBL27426962 0.93 TOP1 (0.84) TOP1MEN1KMT2AALDH1A1GLA
Ammonia Solution, Strong SCHEMBL28299902 0.93 TOP1 (0.84) TOP1MEN1KMT2AALDH1A1GLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025101904-A1 NOREPINEPHRINE TRANSPORTER-TARGETED PRODRUGS FOR CANCER THERAPY THE CHILDREN'S HOSPITAL OF PHILADELPHIA (US) 2025-05-15 WO claimed
WO-2024080726-A1 PHARMACEUTICAL COMPOSITION FOR PREVENTING AND TREATING CANCER, CONTAINING NATURAL KILLER CELLS AND TOPOISOMERASE INHIBITOR AS ACTIVE INGREDIENTS (주) 테라베스트 2024-04-18 WO claimed
CN-110200920-B Reduction-sensitive pharmaceutical composition and preparation and application thereof 东南大学 2022-03-08 CN claimed
CN-110302159-B Reduction sensitive lipid pharmaceutical composition and preparation method and application thereof 东南大学 2021-12-24 CN claimed
EP-1003516-A4 METHODS OF ADMINISTERING CAMPTOTHECIN COMPOUNDS FOR THE TREATMENT OF CANCER WITH REDUCED SIDE EFFECTS UNIV GEORGE WASHINGTON (US) 2006-07-12 EP claimed
US-6635628-B2 Administering camptothecin compounds at an alkaline pH for inhibiting diarrhea side effect of camptothecin compounds THE GEORGE WASHINGTON UNIVERSITY 2003-10-21 US claimed
US-20020193391-A1 Methods of administering camptothecin compounds for the treatment of cancer with reduced side effects BOUSCAREL BERNARD (US) 2002-12-19 US claimed
US-6407117-B1 ADMINISTERING IRINOTECAN HYDROCHLORIDE AND BICARBONATE TO MAINTAIN INTESTINAL LUMEN ALKALINITY AND PREVENT DIARRHEA; AIDS TREATMENT THE GEORGE WASHINGTON UNIVERSITY 2002-06-18 US claimed
EP-1003516-A1 METHODS OF ADMINISTERING CAMPTOTHECIN COMPOUNDS FOR THE TREATMENT OF CANCER WITH REDUCED SIDE EFFECTS The George Washington University (US) 2000-05-31 EP claimed
WO-1999065493-A9 METHODS OF ADMINISTERING CAMPTOTHECIN COMPOUNDS FOR THE TREATMENT OF CANCER WITH REDUCED SIDE EFFECTS UNIV GEORGE WASHINGTON (US) 2000-03-23 WO claimed
WO-1999065493-A1 METHODS OF ADMINISTERING CAMPTOTHECIN COMPOUNDS FOR THE TREATMENT OF CANCER WITH REDUCED SIDE EFFECTS THE GEORGE WASHINGTON UNIVERSITY (US) 1999-12-23 WO claimed
US-RE32518-E Camptothecin derivatives KABUSHIKI KAISHA YAKULT HONSHA (JP) 1987-10-13 US claimed
EP-0056692-B1 7-SUBSTITUTED CAMPTOTHECIN DERIVATIVES AND PROCESS FOR THEIR PREPARATION KABUSHIKI KAISHA YAKULT HONSHA (JP) 1985-08-14 EP claimed
US-4399282-A 7-HYDROXYALKYL DERIVATIVES USING FREE RADICAL CATALYSTS; ANTITUMOR AND -CARCINOGENIC AGENTS; NONTOXIC KABUSHIKI KAISHA YAKULT HONSHA (JP) 1983-08-16 US claimed
EP-0056692-A1 7-Substituted camptothecin derivatives and process for their preparation KABUSHIKI KAISHA YAKULT HONSHA (JP) 1982-07-28 EP claimed
JP-57116076-A None JP disclosed
JP-56012393-A None JP disclosed
EP-0056692-A1 7-Substituted camptothecin derivatives and process for their preparation KABUSHIKI KAISHA YAKULT HONSHA (JP) 1982-07-28 EP disclosed
JP-S57116076-A NOVEL CAMPTOTHECIN DERIVATIVE AND ITS PREPARATION YAKULT HONSHA CO LTD 1982-07-19 JP disclosed
JP-S5612393-A NOVEL CAMPTOTHECIN DERIVATIVE YAKULT HONSHA CO LTD 1981-02-06 JP 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-20020193391-A1 Methods of administering camptothecin compounds for the treatment of cancer with reduced side effects SI, SLC10A2, TOP2A TOP1 4/4885MEN1 1206/4885KMT2A 3584/4885

“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.