(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide
- CAS No.
- 439687-69-1
- Chemical Name:
- (2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide
- Synonyms
- Nelivaptan;NB-415;SSR 149415;SSR 149415 - Nelivaptan;Nelivaptan(SSR-149,415);(2S,4R)-1-[(3R)-5-chloro-1-(2,4-dimethoxyphenyl)sulfonyl-3-(2-methoxyphenyl)-2-oxoindol-3-yl]-4-hydroxy-N,N-dimethylpyrrolidine-2-carboxamide;(2S,4R)-1-((R)-5-Chloro-1-((2,4-dimethoxyphenyl)sulfonyl)-3-(2-methoxyphenyl)-2-oxoindolin-3-yl)-4-hydroxy-N,N-dimethylpyrrolidine-2-carboxamide;(2S,4R)-1-[(3R)-5-Chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-2,3-dihydro-3-(2-methoxyphenyl)-2-oxo-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-2-pyrrolidinecarboxamide;2-PYRROLIDINECARBOXAMIDE, 1-[(3R)-5-CHLORO-1-[(2,4-DIMETHOXYPHENYL)SULFONYL]-2,3-DIHYDRO-3-(2-METHOXYPHENYL)-2-OXO-1H-INDOL-3-YL]-4-HYDROXY-N,N-DIMETHYL-, (2S,4R)-;(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide
- CBNumber:
- CB02448473
- Molecular Formula:
- C30H32ClN3O8S
- Molecular Weight:
- 630.11
- MDL Number:
- MFCD06199090
- MOL File:
- 439687-69-1.mol
- MSDS File:
- SDS
- TDS File:
- TDS
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide Properties
| Boiling point | 799.7±70.0 °C(Predicted) |
|---|---|
| Density | 1.414±0.06 g/cm3(Predicted) |
| storage temp. | Store at -20°C |
| solubility | 63.01mg/ml in DMSO; 63.01mg/ml in ethanol |
| pka | 14.14±0.40(Predicted) |
| form | Solid |
| color | White to off-white |
| FDA UNII | 3TY57MQ4OA |
| UNSPSC Code | 12352200 |
| NACRES | NA.21 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS08 |
|---|---|
| Signal word | Warning |
| Hazard statements | H373 |
| Precautionary statements | P260-P314-P501 |
| WGK Germany | WGK 3 |
| Storage Class | 11 - Combustible Solids |
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Biosynth | PSA68769 | SSR 149415 | 439687-69-1 | 25mg | $877 | 2026-06-04 | Buy |
| Biosynth | PSA68769 | SSR 149415 | 439687-69-1 | 50mg | $1403.5 | 2026-06-04 | Buy |
| Biosynth | PSA68769 | SSR 149415 | 439687-69-1 | 100mg | $2246 | 2026-06-04 | Buy |
| ChemScene | CS-0002429 | Nelivaptan 99.89% | 439687-69-1 | 1mg | $97 | 2026-06-04 | Buy |
| ChemScene | CS-0002429 | Nelivaptan 99.89% | 439687-69-1 | 5mg | $200 | 2026-06-04 | Buy |
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide Chemical Properties,Uses,Production
Uses
SSR 149415 is a vasopressin V1b receptor antagonist.
Biological Activity
SSR149415 is an orally active, selective vasopressin V1b receptor antagonist (human/r at Ki in nM = 1.5/1.3/V1b, 91/1050/V1a, 1412/2897/V2, 174/270/OT) th at inhibits 30 nM AVP-induced Ca2+ response in human and r at V1b CHO transfectants (Ki = 1.26/2.0 nM). SSR149415 suppresses AVP-mediated physiological responses in vivo, including corticotropin secretion (1-30 mg/kg p.o. or i.p. in rats) upon exogenous AVP administration (0.3 μg/kg alone or 0.03 μg/kg with 0.1 μg corticoliberin/kg via i.v.), restraint stress-Induced corticotropin secretion (EC50 = 10 mg/kg i.p. in rats), and in a murine model of anxiety (four-plate test; 1-10 mg/kg i.p. or 3-10 mg/kg p.o. acute or 10 mg/kg/day p.o.).
in vivo
Nelivaptan (1-30 mg/kg; 30 min i.p. or 2 h p.o. before an exogenous AVP injection) inhibits exogenous AVP-induced increase in plasma corticotropin in Sprague-Dawley rats[1].
Nelivaptan (1-10 mg/kg; p.o.; 1, 2, 3, 4, and 6 h before the AVP challenge) produces powerful dose-dependent inhibition of the corticotropin increase in response to exogenous AVP plus corticotropin-releasing factor (CRF) in Sprague-Dawley rats[1].
Nelivaptan (1-10 mg/kg; i.p. 30 min or 60 min before test; or p.o. for 7 days) displays anxiolytic-like activity after acute and 7-day repeated administrations in male NMRI mice [1].
Nelivaptan (30 mg/kg; i.p.; daily for two weeks) retains efficacy in reducing both measured indices of depression-like behavior (learned helplessness and anhedonia), even when neurogenesis is blocked in male Wistar rats with chronic mild stress[2].
| Animal Model: | Male Wistar rats (300-400 g, aged 3 months) with chronic mild stress[2] |
| Dosage: | 30 mg/kg |
| Administration: | Intraperitoneal injection (i.p.); daily for two weeks |
| Result: | Chronic administration reversed learned helplessness and anhedonia even when methylazoxymethanol (MAM) was administered. Attenuated these depressive-like behaviors after 1 week. Restored the density of Ki-67-positive cells to control levels. |
| Animal Model: | Male Sprague-Dawley CD rats (275-300 g)[1] |
| Dosage: | 1, 3, 10, 30 mg/kg |
| Administration: | Intraperitoneal injection (i.p.) or Oral gavage (p.o.); 30 min i.p. or 2 h p.o. before an exogenous AVP injection |
| Result: | Antagonized AVP-induced corticotropin secretion in a dose-dependent manner by both intraperitoneal and oral routes. The inhibition was significant from 10 mg/kg p.o. and 3 mg/kg i.p. upwards. The inhibitory action lasted significantly for more than 2 h at 10 mg/kg i.p. and up to 4 h at 10 mg/kg p.o.. Had no effect on basal corticotropin plasma levels up to 30 mg/kg p.o.. |
| Animal Model: | Male Sprague-Dawley CD rats (275-300 g)[1] |
| Dosage: | 1, 3, 10 mg/kg |
| Administration: | Oral gavage (p.o.); 1, 2, 3, 4, and 6 h before the AVP challenge (10 mg/kg) |
| Result: | Produced powerful dose-dependent inhibition of the corticotropin increase in response to exogenous AVP plus corticoliberin; the effect was significant from the dose of 3 mg/kg p.o.. Complete blockade was achieved at 10 mg/kg. Showed a fast onset of action, the inhibitory effect was maximal at 1 h after administration. The inhibitory effect on corticotropin secretion lasted significantly more than 4 h, demonstrating a long-lasting oral effect in a specific V1b-related model. |
| Animal Model: | Male NMRI mice (20 g)[1] |
| Dosage: | 1, 3, 10 mg/kg |
| Administration: | Intraperitoneal injection (i.p.) or Oral gavage (p.o.); i.p. (1, 3, 10 mg/kg) 30 min or 60 min befeore; p.o. (10 mg/kg) for 7 days, |
| Result: | In the acute experiments, i.p. and p.o. compound increased the number of punished crossings showing marked anxiolytic effects. Post hoc analysis revealed that these effects reached statistical significance from 3 mg/kg p.o. and i.p. The anxiolytic-like activity was still significantly maintained when given repeatedly at 10 mg/kg p.o. for 7 days. The oral time course of the anxiolytic-like action performed at 10 mg/kg indicated that effects lasted for more than 4 h. |
storage
Store at -20°C
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide Preparation Products And Raw materials
Raw materials
Preparation Products
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Shanghai EFE Biological Technology Co., Ltd. | 021-65675885 18964387627 | info@efebio.com | China | 9799 | 58 |
| Shanghai YuanYe Biotechnology Co., Ltd. | 15026964105 | 2881489226@qq.com | China | 89667 | 60 |
| Shanghai Hongye Biotechnology Co. Ltd | 400-9205774 400-920-5774 | sales@glpbio.cn | China | 6705 | 58 |
| TargetMol Chemicals Inc. | +1-781-999-5354; +1-00000000000 | marketing@targetmol.com | United States | 32431 | 58 |
| Sichuan Changdexiangshun Co., Ltd. | 13989459766;18781211904 | 348632238@qq.com | China | 176 | 58 |
| TargetMol Chemicals Inc. | 4008200310 15002144251 | marketing@tsbiochem.com | China | 24951 | 58 |
| Suzhou Meishi Biotechnology Co., Ltd. | 1173954148q | meishipharma@126.com | China | 20027 | 58 |
| Hangzhou Runyan Medical Technology Co., LTD | 571-13989459766 18112526015 | sales@runyanpharma.com | China | 496 | 58 |
| Beijing Boorsen Biotechnology Co., Ltd | 400-901-9800 18611424007 | cis@bioss.com.cn | China | 9185 | 58 |
| Shanghai Aladdin Biochemical Technology Co.,Ltd. | 6206333 13167063860 | anhua.mao@aladdin-e.com | China | 43293 | 58 |
View Lastest Price from (2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
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2026-07-15 | Nelivaptan
439687-69-1
|
$71.00-220.00 | 99.46% | 10g | TargetMol Chemicals Inc. | ||
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2025-08-21 | Nelivaptan(SSR-149415)
439687-69-1
|
1g | 99.0%min. HPLC | 10000 | HangZhou RunYan Pharma Technology Co.,LTD. |
-

- Nelivaptan
439687-69-1
- $71.00-220.00
- 99.46%
- TargetMol Chemicals Inc.
-

- Nelivaptan(SSR-149415)
439687-69-1
- 99.0%min. HPLC
- HangZhou RunYan Pharma Technology Co.,LTD.
(2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide Spectrum
439687-69-1((2S,4R)-1-[(R)-5-Chloro-1-(2,4-dimethoxy-benzenesulfonyl)-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-pyrrolidine-2-carboxylic acid dimethylamide)Related Search:
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