SCHEMBL7216296

SCHEMBL7216296

O=C(O)c1cc2c(cc1Br)OCO2

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.73
ALDH1A1 P00352 3/20 0.48
MAPK1 P28482 2/20 0.48
MAPT P10636 2/20 0.48
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
HPGD P15428 3/20 0.45
LCK P06239 1/20 0.44
FYN P06241 1/20 0.44
SRD5A2 P31213 1/20 0.43
CA12 O43570 1/20 0.43
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43
CA3 P07451 1/20 0.43
CA4 P22748 1/20 0.43
CA6 P23280 1/20 0.43
CA5A P35218 1/20 0.43
CA7 P43166 1/20 0.43
CA9 Q16790 1/20 0.43
CA13 Q8N1Q1 1/20 0.43

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
SCHEMBL30617194 1.00 SMN1; SMN2 (0.73) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL14907130 0.88 SMN1; SMN2 (0.86) SMN1; SMN2ALDH1A1MAPTMEN1KMT2A
SCHEMBL29921207 0.85 ALDH1A1 (0.57) SMN1; SMN2ALDH1A1MAPK1MEN1KMT2A
SCHEMBL7370339 0.85 ALDH1A1 (0.57) SMN1; SMN2ALDH1A1MAPK1MEN1KMT2A
SCHEMBL9016652 0.82 SMN1; SMN2 (0.51) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL11832759 0.82 SMN1; SMN2 (0.51) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL10913744 0.82 SMN1; SMN2 (0.50) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL11856611 0.79 MAPT (0.55) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL17782662 0.78 KDM4E (0.53) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1
SCHEMBL20749465 0.78 SMN1; SMN2 (0.47) SMN1; SMN2ALDH1A1MAPK1MAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4304588-A1 COMPOUNDS HAVING TETRAHYDROINDOLIZINE-1-CARBOXAMIDE AS BCL-2 INHIBITORS Eil Therapeutics, Inc. (US) 2024-01-17 EP disclosed
CN-116981458-A Compounds with tetrahydroindole-1-carboxamides as BCL-2 inhibitors 伊尔治疗学股份有限公司 2023-10-31 CN disclosed
WO-2023160509-A1 AMIDINE DERIVATIVE COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 中国科学院上海药物研究所 2023-08-31 WO disclosed
US-11697650-B2 Compounds having tetrahydroindolizine-1-carboxamide as BCL-2 inhibitors Eil Therapeutics, Inc. (US) 2023-07-11 US disclosed
US-11697650-B2 Compounds having tetrahydroindolizine-1-carboxamide as BCL-2 inhibitors Eil Therapeutics, Inc. (US) 2023-07-11 US disclosed
US-11697650-B2 Compounds having tetrahydroindolizine-1-carboxamide as BCL-2 inhibitors Eil Therapeutics, Inc. (US) 2023-07-11 US disclosed
US-20230192622-A1 ANTI-SARS-COV-2 DRUG ONCOLYS BIOPHARMA, INC. (JP) 2023-06-22 US disclosed
EP-4154884-A1 ANTI-SARS-COV-2 DURG Oncolys BioPharma, Inc. (JP) 2023-03-29 EP disclosed
US-20220289745-A1 COMPOUNDS HAVING TETRAHYDROINDOLIZINE-1-CARBOXAMIDE AS BCL-2 INHIBITORS EIL TERAPEUTICS, INC. 2022-09-15 US disclosed
US-10662173-B2 Indole and pyrrole compounds, a process for their preparation and pharmaceutical compositions containing them LES LABORATOIRES SERVIER (FR) 2020-05-26 US disclosed
US-20120316342-A1 THERAPEUTIC AGENT FOR HEPATITIS C ONCOLYS BIOPHARMA, INC. (JP) 2012-12-13 US disclosed
EP-2532652-A1 THERAPEUTIC AGENT FOR HEPATITIS C Kagoshima University (JP) 2012-12-12 EP disclosed
US-6620807-B1 Temporary delay of urination for treatment of diabetes, urinary incontinence, bleeding or coagulation disorders WYETH 2003-09-16 US disclosed
EP-1149104-B1 PYRROLOBENZODIAZEPINE CARBOXYAMIDE VASOPRESSIN AGONISTS WYETH CORP (US) 2002-12-11 EP disclosed
CN-1339035-A Pyridobenzodiazepine and pyridobenzoxazepine carboxyamide vasopressin agonists AMERICAN HOME PROD (US) 2002-03-06 CN disclosed
US-6344451-B1 DIABETES INSIPIDUS, NOCTURNAL ENURESIS, NOCTURIA, URINARY INCONTINENCE, BLEEDING AND COAGULATION DISORDERS, OR TEMPORARY DELAY OF URINATION AMERICAN HOME PRODUCTS 2002-02-05 US disclosed
EP-1149097-A2 PYRIDOBENZODIAZEPINE AND PYRIDOBENZOXAZEPINE CARBOXYAMIDE VASOPRESSIN AGONISTS AMERICAN HOME PRODUCTS CORPORATION (US) 2001-10-31 EP disclosed
EP-1149104-A2 PYRROLOBENZODIAZEPINE CARBOXYAMIDE VASOPRESSIN AGONISTS AMERICAN HOME PRODUCTS CORPORATION (US) 2001-10-31 EP disclosed
WO-2000046225-A2 PYRIDOBENZODIAZEPINE AND PYRIDOBENZOXAZEPINE CARBOXYAMIDE VASOPRESSIN AGONISTS AMERICAN HOME PRODUCTS CORPORATION (US) 2000-08-10 WO disclosed
WO-2000046228-A2 PYRROLOBENZODIAZEPINE CARBOXYAMIDE VASOPRESSIN AGONISTS AMERICAN HOME PRODUCTS CORPORATION (US) 2000-08-10 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 (5 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-10662173-B2 Indole and pyrrole compounds, a process for their preparation and pharmaceutical compositions containing them RB1, IDO1, BCL2A1 SMN1; SMN2 3448/4885ALDH1A1 1103/4885MAPK1 2938/4885
US-20230192622-A1 ANTI-SARS-COV-2 DRUG ACE2, ACE, SARS1 SMN1; SMN2 4289/4885ALDH1A1 3243/4885MAPK1 855/4885
US-20220289745-A1 COMPOUNDS HAVING TETRAHYDROINDOLIZINE-1-CARBOXAMIDE AS BCL-2 INHIBITORS BCL2, BCL2L1, BCL2A1 SMN1; SMN2 2191/4885ALDH1A1 758/4885MAPK1 1950/4885
US-11697650-B2 Compounds having tetrahydroindolizine-1-carboxamide as BCL-2 inhibitors BCL2, BCL2L1, BCL2A1 SMN1; SMN2 2191/4885ALDH1A1 758/4885MAPK1 1950/4885
US-20120316342-A1 THERAPEUTIC AGENT FOR HEPATITIS C HAVCR2, SLC10A1, FABP1 SMN1; SMN2 4017/4885ALDH1A1 251/4885MAPK1 1243/4885

“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.