Pygenic Acid A

Pygenic Acid A

SCHEMBL4962201

C[C@H]1[C@H](C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@H]12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD11B1 P28845 3/20 1.00
▸ POLB P06746 3/20 1.00
▸ PTPN2 P17706 2/20 1.00
▸ PTPN1 P18031 2/20 1.00
▸ PTPN6 P29350 2/20 1.00
▸ GPBAR1 Q8TDU6 2/20 1.00
▸ USP7 Q93009 2/20 1.00
▸ PYGM P11217 1/20 1.00
▸ HTT P42858 1/20 1.00
▸ AKR1B10 O60218 2/20 0.80
▸ AKR1B1 P15121 2/20 0.80
▸ GABRP O00591 1/20 0.80
▸ GABRD O14764 1/20 0.80
▸ GABRA1 P14867 1/20 0.80
▸ GABRB1 P18505 1/20 0.80
▸ GABRG2 P18507 1/20 0.80
▸ GABRB3 P28472 1/20 0.80
▸ GABRA5 P31644 1/20 0.80
▸ GABRA3 P34903 1/20 0.80
▸ GABRA2 P47869 1/20 0.80

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
Corosolic Acid SCHEMBL13735311 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL4456542 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL18428539 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL1157257 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL13629647 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL12181488 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL14628105 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL13629630 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL22027588 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6
Corosolic Acid SCHEMBL4456541 1.00 HSD11B1 (1.00) HSD11B1POLBPTPN2PTPN1PTPN6

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116660543-A Diagnostic and prognostic markers for nonalcoholic fatty liver disease and uses thereof 中国人民解放军陆军军医大学第一附属医院 2023-08-29 — — CN claimed
CN-113975283-B Anti-angiogenic composition containing sepsis a isolated from Prunella vulgaris as active ingredient 韩国韩医药振兴院 2024-12-10 — — CN disclosed
US-20200163983-A1 SAPONIN COMPOUND TARGETING PD-1 AND APPLICATION THEREOF SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2020-05-28 — — US disclosed
US-20180118657-A1 METHODS FOR INHIBITING MUSCLE ATROPHY UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2018-05-03 — — US disclosed
US-20130203712-A1 METHODS FOR INHIBITING MUSCLE ATROPHY UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2013-08-08 — — US disclosed
EP-0914139-B1 ANTIVIRAL AGENTS FROM PLANT EXTRACTS AND USE FOR TREATMENT OF VIRAL INFECTIONS TSAI HSIU-HSIEN (TW) 2008-02-27 — — EP disclosed
US-20060235078-A1 Insulin secretion potentiator USE-TECHNO CORPORATION 2006-10-19 — — US disclosed
EP-1674089-A1 ACCELERATOR FOR INITIAL INSULIN SECRETION Use-Techno Corporation (JP) 2006-06-28 — — EP disclosed
WO-2006054370-A1 GLUCONEOGENESIS INHIBITING AGENT USE-TECHNO CORPORATION (JP) 2006-05-26 — — WO disclosed
US-20050143464-A1 With low side effects, which rapidly stimulate early insulin secretion and suppress blood glucose increase only at mealtimes; antidiabetic agent; triterpene acids or alcohols with picene ring; corosolic acids; oleanene acids; ursenoic acids; banaba plant extracts USE-TECHNO CORPORATION 2005-06-30 — — US disclosed
US-6214350-B1 Process for preparing an anti-viral medicinal product from plant extracts HWANG SHIE-MING (US) 2001-04-10 — — US disclosed
EP-0914139-A2 ANTIVIRAL AGENTS FROM PLANT EXTRACTS AND USE FOR TREATMENT OF VIRAL INFECTIONS Sage, R & D (US) 1999-05-12 — — EP disclosed
WO-1998001144-A9 ANTIVIRAL AGENTS FROM PLANT EXTRACTS AND USE FOR TREATMENT OF VIRAL INFECTIONS — 1999-03-18 — — WO disclosed
US-5837257-A COMPOSITIONS DERIVED FROM CHINESE HERBAL MEDICINES, MEDICINAL PLANTS, AND EXTRACTS THEREOF SAGE R&D (US) 1998-11-17 — — US disclosed
WO-1998001144-A1 ANTIVIRAL AGENTS FROM PLANT EXTRACTS AND USE FOR TREATMENT OF VIRAL INFECTIONS SAGE R & D (US) 1998-01-15 — — 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-20050143464-A1 With low side effects, which rapidly stimulate early insulin secretion and suppress blood glucose increase only at mealtimes; antidiabetic agent; triterpene acids or alcohols with picene ring; corosolic acids; oleanene acids; ursenoic acids; banaba plant extracts GPR119, IRS1, AMY1A HSD11B1 18/4885POLB 2537/4885PTPN2 2179/4885
US-20200163983-A1 SAPONIN COMPOUND TARGETING PD-1 AND APPLICATION THEREOF PDCD1, CD274, PDCD1LG2 HSD11B1 110/4885POLB 3215/4885PTPN2 235/4885
US-20060235078-A1 Insulin secretion potentiator IAPP, GPR119, IRS1 HSD11B1 36/4885POLB 4362/4885PTPN2 1100/4885
US-20180118657-A1 METHODS FOR INHIBITING MUSCLE ATROPHY TNNC1, PYGM, GYS1 HSD11B1 130/4885POLB 3218/4885PTPN2 4663/4885
US-20130203712-A1 METHODS FOR INHIBITING MUSCLE ATROPHY TNNC1, PYGM, GYS1 HSD11B1 130/4885POLB 3218/4885PTPN2 4663/4885

“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.

Send feedback