Gestodene
drugOn this page
Also known as GestodenoSH B 331SH-B-331SID144205785SID170466131GestodeneÊGestodeneÂ
Summary
Gestodene (CHEMBL1213583) is a phase-3 clinical-stage small molecule.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Clinical trials: 13
- Chemistry: 310.4 Da · C21H26O2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1213583 |
| Name | Gestodene |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 3033968 |
| Molecular formula | C21H26O2 |
| Molecular weight | 310.4 |
| InChIKey | SIGSPDASOTUPFS-XUDSTZEESA-N |
SMILES: CC[C@]12CC[C@H]3[C@H]([C@@H]1C=C[C@]2(C#C)O)CCC4=CC(=O)CC[C@H]34
IUPAC name: (8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-1,2,6,7,8,9,10,11,12,14-decahydrocyclopenta[a]phenanthren-3-one
Also known as: Gestodene, Gestodeno, SH B 331, SH-B-331, GESTODENE, SID144205785, SID170466131, gestodene, GestodeneÊ, GestodeneÂ
Patent coverage: 1,576 distinct patent families (5,754 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 6 (assay-derived). Sample: Androgen receptor, Estrogen receptor, Progesterone receptor, Sodium-dependent serotonin transporter, Mu-type opioid receptor, Gamma-aminobutyric acid receptor subunit alpha-1.
Bioactivity
ChEMBL activities: 5 potent at pChembl ≥ 5 of 6 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| AR | 8.52 | AC50 | 3 | nM | CHEMBL_ACT_25203428 |
| PGR | 8.52 | AC50 | 3 | nM | CHEMBL_ACT_25204361 |
| ESR1 | 5.92 | AC50 | 1200 | nM | CHEMBL_ACT_25138928 |
| P62813 | 5.67 | AC50 | 2160 | nM | CHEMBL_ACT_25207931 |
| SLC6A4 | 5.34 | AC50 | 4590 | nM | CHEMBL_ACT_25151397 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
0 indications (0 at ChEMBL trial phase 4).
Clinical trials
Total trials: 13.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 6 |
| PHASE3 | 3 |
| Not specified | 2 |
| PHASE1/PHASE2 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00910637 | PHASE3 | COMPLETED | Study Investigating the Efficacy and Safety of a Contraceptive Patch for 13 Cycles |
| NCT00914693 | PHASE3 | COMPLETED | EU/LA Pearl Index Study - Transdermal Contraceptive Patch |
| NCT00920985 | PHASE3 | COMPLETED | US Cycle Control and Blood Pressure Study |
| NCT00729404 | PHASE2 | TERMINATED | Inhibition of Ovulation, Patch, Ethinylestradiol and Gestodene |
| NCT00873483 | PHASE2 | COMPLETED | US Ovulation Inhibition Study in Obese Women |
| NCT00915915 | PHASE2 | COMPLETED | Inhibition of Ovulation and Pharmacokinetics of Transdermal Ethinylestradiol (EE) and Gestodene (GSD) |
| NCT00933179 | PHASE2 | COMPLETED | FC Patch Low: Metabolism Study |
| NCT01204190 | PHASE2 | COMPLETED | Investigation of Three Contraceptive Hormone Patches in Regard to Inhibition of Ovulation Following Application Over 3 Treatment Cycles in Healthy, Young Women. |
| NCT02550977 | PHASE2 | COMPLETED | Russia/Ukraine Suppression of Ovarian Activity Study |
| NCT03881904 | PHASE1/PHASE2 | UNKNOWN | OCP Pretreatment in PCOS Patients Undergoing ICSI Using Antagonist Protocol |
| NCT01083264 | PHASE1 | COMPLETED | Relative Bioavailability, Transdermally Administered EE and GSD, 3 Applications Sites |
| NCT06396208 | Not specified | COMPLETED | Quick-starting of a Quadriphasic Contraceptive Pills, 1 - 3 mg Estradiol Valerate/ 2 - 3 mg Dienogest VS 20 mcg Ethinylestradiol/75 mcg Gestodene Focusing on Ovulation Inhibition |
| NCT06396221 | Not specified | COMPLETED | Quick-starting of a New Combined Hormonal Contraceptive Pills, 15 mg Estetrol/3 mg Drospirenone VS 20 mcg Ethinylestradiol/75 mcg Gestodene Focusing on Ovulation Inhibition |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.